{ "count" : 123422, "data" : [ { "id" : "6a2c8d9f74d8ee00a097978f", "title" : "Director, Quality Assurance, GCP", "company" : "Xenon Pharmaceuticals", "industry" : "R&D Operations", "salary" : { "min" : 216400.0, "max" : 234900.0, "currency" : "USD", "frequency" : "Yearly" }, "location" : "Boston", "locations" : [ "Boston" ], "timestamp" : "2026-06-15T08:09:19.942", "fingerprint" : "06bd59d556e5791cebd8f981c6fe98c23f42be4668e5b9d4b8ed5cc7de5b74ae", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/xenon/166325d2-cf3d-4b81-bdb5-e8ee120e7f60/application", "externalId" : "166325d2-cf3d-4b81-bdb5-e8ee120e7f60", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Boston", "state" : "Massachusetts", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "42.3588336,-71.0578303" } ], "locationText" : "Boston, Massachusetts, United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "professionalSkills" : [ "Quality oversight", "Compliance interpretation", "Root cause analysis", "Budget management" ], "hardSkillsList" : [ "GLP auditing", "GCP auditing", "Regulatory inspections", "Quality systems development" ], "softSkillsList" : [ "Leadership", "Mentoring" ], "hardSkills" : [ { "name" : "GLP auditing", "level" : "intermediate" }, { "name" : "GCP auditing", "level" : "intermediate" }, { "name" : "Regulatory inspections", "level" : "intermediate" }, { "name" : "Quality systems development", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "Quality Assurance, GCP, GLP", "majorSkillsList" : [ "Quality Assurance", "GCP", "GLP" ], "coreResponsibilities" : "Lead quality oversight of GLP programs, Manage GLP audit program, Develop annual GLP audit plan, Lead quality oversight of early phase clinical programs, Provide GLP/GCP compliance interpretation, Provide GLP/GCP consultation, Provide GLP/GCP training, Provide root cause analysis, Identify critical quality issues, Escalate critical quality issues, Assist with regulatory inspection preparation, Coordinate regulatory inspections, Maintain cross-functional communications, Collaborate on quality principles, Collaborate on regulatory requirements, Ensure compliance with legislation, Ensure compliance with regulations, Develop GLP/GCP objectives, Propose GLP/GCP objectives, Plan budget proposals, Manage approved budgets, Recruit direct reports, Lead direct reports, Direct direct reports, Develop direct reports, Coach direct reports, Evaluate direct reports", "teamCollaboration" : "Cross-functional communications; Internal stakeholders; External stakeholders; Multidisciplinary team", "projectManagementSkills" : [ "Project teams", "Critical milestones", "Timelines", "Budgets" ], "domainKnowledge" : "Neuroscience; Drug discovery; Clinical development; Ion channel biology; Human genetics; Biopharmaceutical industry; GLP regulations; GCP regulations; GVP regulations; Drug development process", "domainList" : [ "neuroscience", "drug-discovery", "clinical-development", "ion-channel-biology", "human-genetics", "biopharmaceutical-industry", "glp-regulations", "gcp-regulations", "gvp-regulations", "drug-development-process" ], "domainSpecificKnowledge" : [ "Neuroscience", "Drug discovery", "Clinical development", "Ion channel biology", "Human genetics", "Biopharmaceutical industry", "GLP regulations", "GCP regulations", "GVP regulations", "Drug development process" ], "communicationSkills" : "Interpersonal skills; Excellent communication; Verbal communication; Written communication", "continuousLearning" : "Training; Learning & Development; Tuition Assistance", "problemSolvingSkills" : "Root cause analysis", "qualificationsBasic" : "Clinical/non-clinical quality background, 5+ years management experience, GLP/GCP/GVP regulations knowledge, Drug development process understanding, Audit experience, CAPA experience, Risk evaluation experience, Strategic thinking ability, Organizational skills, Project team driving ability, Hands on work willingness, Professional communication, Clear communication, Concise communication, Consistent communication, Independent work ability, Collaborative work ability, People management skills, Mentorship skills, Negotiation skills, Conflict resolution skills", "qualificationsPreferred" : "Experience interacting with regulatory inspectorates", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Who We Are: Xenon Pharmaceuticals (NASDAQ:XENE https://www.nasdaq.com/market-activity/stocks/xene) is a neuroscience-focused biopharmaceutical company dedicated to drug discovery, clinical development, and commercialization of life-changing therapeutics for patients in need. We are looking for great people who thrive in a respectful, collaborative, inclusive, and productive culture to join the Xenon team. What We Do: We are advancing an exciting product pipeline https://xenon-pharma.com/pipeline to address indications with high unmet medical need, including epilepsy, depression and pain. Our Phase 3 azetukalner program represents the most advanced, clinically validated potassium channel modulator in late-stage clinical development for multiple indications. In March 2026, we announced positive topline data from our Phase 3 X-TOLE2 study of azetukalner in focal onset seizures (FOS), and we anticipate submitting a New Drug Application to the Food and Drug Administration in the third quarter of 2026. Our Phase 3 epilepsy program also includes a second FOS study, X-TOLE3, which would support regulatory submissions outside the U.S., and the X-ACKT study in primary generalized tonic-clonic seizures, which would support regulatory submissions for an additional epilepsy indication. We also have multiple Phase 3 azetukalner clinical trials underway in major depressive disorder (MDD) and bipolar depression (BPD), based on topline data from our Phase 2 X-NOVA clinical trial. In addition, we are proud of our strong heritage in human genetics, deep understanding of ion channel biology, and expertise in novel chemistries to enable potent, selective ion channel targeting. We continue to advance an early-stage pipeline of novel therapeutic candidates, including Phase 1 studies for XEN1701 (targeting Nav1.7) and XEN1120 (targeting Kv7), which are important pain targets. Backed by a strong balance sheet to support our growth plans, we continue to build a fully integrated, premier neuroscience company with strong discovery, clinical development, corporate, and commercial operations. About the Role: We are seeking a Director, Quality Assurance, GCP/GLP to join our team. We are building our Quality function to support Xenon’s clinical development programs, as well as expand quality initiatives across the company. This person will provide Quality leadership primarily in support of early-stage clinical programs (pre-phase 3) and non-clinical studies. This position will contribute to inspection readiness initiatives and for ensuring compliance within R&D Program. The successful candidate must have a strong clinical/non-clinical quality background, including providing Quality support for study teams, auditing, and inspections. This position must have exceptional interpersonal skills, excellent communication skills, and a collaborative and pragmatic approach to Quality. This position reports to the Executive Director, Quality Assurance, GCP and will be based out of Boston, MA, USA in our Needham office. We will consider remote locations for exceptional candidates. The level of the position will be commensurate with the candidate’s education and industry experience. Hybrid positions require a minimum of two onsite days per week. RESPONSIBILITIES: · Lead and manage quality oversight of the Company’s GLP programs, including the GLP audit program, collaborating with Quality Systems to develop an annual GLP audit plan. · Lead and manage quality oversight of the Company’s early phase clinical programs. · Provide expert GLP/GCP compliance interpretation, consultation, training, root cause analysis, and other supportive services necessary to maintain and improve the quality of the Company’s R&D programs to safeguard study participants’ safety and rights and ensure the quality, integrity, and credibility of data generated. · Identify and escalate critical quality issues appropriately to QA Management. · Assist with the preparation and coordination of regulatory inspections held remotely and onsite at the Company’s offices, clinical trial sites, and contract service provider facilities, as needed. · Maintain respectful, inclusive, and effective cross-functional communications, collaborating with internal and external stakeholders on strategy and implementation of quality principles and regulatory requirements while remaining independent. · Ensure compliance with relevant legislation and regulations. · Develop and propose short- and long-term objectives for the GLP/GCP functions in accordance with overall Company and Quality strategies. · Plan and manage budget proposals and approved budgets in accordance with the Company’s strategic and operating plans and Finance policies. · Recruit, lead, direct, develop, coach and evaluate direct reports, if any, in accordance with the Company’s Human Resource policies and practices · Act in accordance with Company policies, including, for example, the Code of Business Conduct and Ethics and ensure policies are understood and followed by direct reports, if any · Other duties as assigned QUALIFICATIONS: · Bachelor’s degree in a scientific or health field with at least 10 years of GxP QA experience, 8+ years GCP QA, supporting both development and commercial programs in the pharmaceutical or biotechnology industry. · A minimum of 5 years’ management level experience in a pharma or biotech environment. Job level commensurate with years of experience. · Contemporary knowledge of GLP/GCP/GVP regulations, guidelines, current industry trends, standards, and methodologies. · Experience interacting with regulatory inspectorates (e.g., FDA, Health Canada, EMA, MHRA) is desirable. · Sound understanding of all phases of the drug development process and the interdependencies with other functional areas. · Experience in conducting audits, adapting issues into effective CAPAs, and evaluating trends to mitigate risks. · Ability to prioritize work effectively to manage several complex projects in parallel, and successfully achieve critical milestones and expected deliverables within established timelines and budgets. · Must be able to demonstrate strategic thinking, excellent organizational skills and be able to drive project teams forward while having willingness to do hands on work to achieve goals. · Demonstrated ability to interact professionally and communicate clearly, concisely, and consistently both verbally and in writing with internal and external stakeholders. · Proven ability to work independently and collaboratively as part of a multidisciplinary team. · Proficient people management skills including mentorship, negotiation, and conflict resolution. Our Total Rewards program includes base salary, target bonus, and stock options, as well as a full range of benefits including medical, dental, vision, short-& long-term disability, accidental death & dismemberment, and life insurance programs, Employee Assistance Program, travel insurance, and retirement savings programs with company matching contributions. Xenon encourages time to rest and re-charge through vacation, personal days, sick days, and an end-of-year company shutdown. Xenon highly values employee development and has an expanding Training, Learning & Development program, including a Tuition Assistance program for advanced degrees.", "summaryDescription" : "Director, Quality Assurance, GCP at Xenon Pharmaceuticals. Skills: Quality Assurance, GCP, GLP. Lead quality oversight of GLP programs. Manage GLP audit program", "createdAt" : "2026-06-14T03:12:00.269", "lastUpdated" : "2026-06-15T08:09:19.942", "ingestTimestamp" : "2026-06-14T03:12:00.269", "mongoId" : "6a2c8d9f74d8ee00a097978f", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 216400, "salaryAnnualMax" : 234900, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "GLP auditing", "GCP auditing", "Regulatory inspections", "Quality systems development", "Leadership", "Mentoring", "Quality Assurance", "GCP", "GLP", "Quality oversight", "Compliance interpretation", "Root cause analysis", "Budget management", "Project teams", "Critical milestones", "Timelines", "Budgets", "Neuroscience", "Drug discovery", "Clinical development", "Ion channel biology", "Human genetics", "Biopharmaceutical industry", "GLP regulations", "GCP regulations", "GVP regulations", "Drug development process" ], "skillCount" : 27, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 1632.9574, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.98 }, { "id" : "6a306f60f292fd229cfe83b2", "title" : "Director of Quality", "company" : "Gather AI", "industry" : "Logistics", "salary" : { "min" : 175000.0, "max" : 250000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Director of Quality in Pittsburgh, adjusted for logistics industry and company size." }, "location" : "Pittsburgh, Pennsylvania, United States", "locations" : [ "Pittsburgh", "Pennsylvania", "United States" ], "timestamp" : "2026-06-16T13:26:07.603", "fingerprint" : "2b4e858d552e4aaeccd207d22c6eeb927c8028e1430b970cbf99ce37ed7ea10f", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/gatherai/jobs/5160301007", "externalId" : "5160301007", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Pittsburgh", "state" : "Pennsylvania", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.4406968,-80.0025666" } ], "locationText" : "Pittsburgh, Pennsylvania, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceLevel" : "Director", "technicalSkills" : "Python, CI/CD, Pytest, Docker, AWS, GCP, Robotics simulation, ML model evaluation", "professionalSkills" : [ "System design", "Release management" ], "hardSkillsList" : [ "Test automation", "Model evaluation", "Data pipeline validation", "Hardware-in-the-loop", "Robotics simulation", "ML model evaluation" ], "softSkillsList" : [ "Leadership", "Mentoring" ], "hardSkills" : [ { "name" : "Test automation", "level" : "intermediate" }, { "name" : "Model evaluation", "level" : "intermediate" }, { "name" : "Data pipeline validation", "level" : "intermediate" }, { "name" : "Hardware-in-the-loop", "level" : "intermediate" }, { "name" : "Robotics simulation", "level" : "intermediate" }, { "name" : "ML model evaluation", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "Quality Assurance, AI/ML, Robotics, Cloud Platform", "majorSkillsList" : [ "Quality Assurance", "AI/ML", "Robotics", "Cloud Platform" ], "coreResponsibilities" : "Own and evolve QA strategy across drone hardware,, Establish release qualification gates for full stack, Build automated test infrastructure, Build CI/CD test gates, Build API and UI regression tests, Build data pipeline validation, Build hardware-in-the-loop infrastructure, Build simulation for physical systems, Stand up AI-assisted QA pipeline, Implement LLM-driven test generation, Implement automated failure triage, Implement model output grading, Implement AI-driven exploratory testing, Lead, mentor, and level up distributed QA team, Develop QA Manager, Grow team with automation engineers, Grow team with high-judgment manual testers, Establish ML/perception model evaluation methodology, Establish release qualification criteria for models, Partner cross-functionally with engineering, Partner cross-functionally with autonomy, Partner cross-functionally with cloud, Partner cross-functionally with field ops, Align QA with deployment realities, Align QA with customer-reported quality issues", "teamCollaboration" : "Distributed US and India team; Cross-functional with engineering; Cross-functional with autonomy; Cross-functional with cloud; Cross-functional with field ops", "projectManagementSkills" : [ "Release qualification gates" ], "domainKnowledge" : "Warehouse intelligence; Robotics; Supply chain; Computer vision; ML models; Cloud platform; Embedded systems; SaaS platform", "domainList" : [ "warehouse-intelligence", "robotics", "supply-chain", "computer-vision", "ml-models", "cloud-platform", "embedded-systems", "saas-platform" ], "domainSpecificKnowledge" : [ "Warehouse intelligence", "Robotics", "Supply chain", "Computer vision", "ML models", "Cloud platform", "Embedded systems", "SaaS platform" ], "toolProficiency" : [ "GitHub Actions", "Jenkins", "Docker", "AWS", "GCP", "Gazebo", "Isaac Sim" ], "innovationCreativity" : "AI-assisted QA pipeline", "problemSolvingSkills" : "Automated failure triage; Root cause analysis", "qualificationsBasic" : "10+ years in QA, 5+ years leading QA teams, Demonstrated breadth across at least two of: hardware/embedded systems QA, ML/computer vision model evaluation, cloud/fullstack/SaaS platform QA, Proven track record of replacing manual test cycles with automation, instrumentation, or AI grading, Experience managing geographically distributed team (US + India or equivalent), Hands-on technical depth: Python, Hands-on technical depth: CI/CD, Hands-on technical depth: pytest, Hands-on technical depth: Docker, Hands-on technical depth: AWS or GCP, Familiarity with at least one of hardware-in-the-loop, robotics simulation, or ML model evaluation harnesses, Pittsburgh-based or willing to relocate", "qualificationsPreferred" : "Hardware QA or field reliability experience with sensors, cameras, embedded devices, drones, or robotics, Experience with simulation-based testing for robotics or perception systems, Background in warehouse, logistics, or industrial deployment environments, Experience building or operating QA for multi-tenant SaaS platform at scale", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "About Us Are you ready to build the future of supply chain? At Gather AI, we’re not just creating software; we’re pioneering a new era of warehouse intelligence. We’ve developed a groundbreaking, vision-powered platform that uses autonomous drones and existing equipment to capture real-time data, completely digitizing workflows that have historically been manual and error-prone. This means facilities operate smarter, safer, and more efficiently, ultimately redefining “on-time, in full” delivery. If you’re looking for an opportunity to contribute to truly transformative technology and make a significant impact in a vital industry, Gather AI is the place for you. We’re leading the charge in the rapidly evolving robotics industry, and we invite you to join us in reshaping the global supply chain, one intelligent warehouse at a time. About the Team Quality at Gather AI spans three genuinely distinct surfaces: drones flying in warehouses, camera-based MHE Vision systems installed on forklifts and at dock doors, and a customer-facing cloud platform that ingests it all and turns it into inventory intelligence. Our QA team — currently anchored by a QA Manager and engineering team primarily based in India — has been doing strong work. But as our product lines scale and our engineering org accelerates with AI tooling, we need a Director who can raise the entire function to match. About the Role Most QA Director roles hand you a legacy function and ask you to keep the lights on. This one hands you a genuine mandate: build the QA strategy for an AI-first robotics company from the ground up — across hardware, ML models, and cloud software simultaneously. As our Director of Quality Assurance, you will own the full QA surface: automated test infrastructure for drone flight and docking systems, perception model regression and evaluation, and cloud/API/UI regression for the customer platform. You’ll lead a distributed US and India team, establish release qualification gates that span hardware-to-cloud, and build an AI-assisted QA pipeline that scales throughput as the engineering org’s velocity grows. This is a role with executive visibility, real authority, and the rare opportunity to define what “quality” means at a company where the product is this technically diverse. What You’ll Do Own and evolve QA strategy across all three product surfaces — drone hardware and flight systems, MHE Vision perception, and the cloud/fullstack customer platform — including release qualification gates that span the full stack Build automated test infrastructure from a low baseline: CI/CD test gates, API and UI regression, data pipeline validation, hardware-in-the-loop, and simulation for physical systems Stand up an AI-assisted QA pipeline — LLM-driven test generation, automated failure triage, model output grading, and AI-driven exploratory testing — to scale QA throughput alongside an AI-accelerated engineering org Lead, mentor, and level up the distributed QA team across the US and India, including directly developing the existing QA Manager and growing the team with a deliberate mix of automation engineers and high-judgment manual testers Establish ML/perception model evaluation methodology and release qualification criteria, working directly with ML and autonomy leads to qualify model upgrades for production Partner cross-functionally with engineering, autonomy, cloud, and field ops to align QA with deployment realities and customer-reported quality issues What You’ll Need 10+ years in QA or test engineering with production systems at scale, including 5+ years leading QA, SDET, or test engineering teams Demonstrated breadth across at least two of: hardware/embedded systems QA, ML/computer vision model evaluation, and cloud/fullstack/SaaS platform QA — single-domain specialists will not have the range this role requires Proven track record of replacing manual test cycles with automation, instrumentation, or AI grading — and a clear philosophy for where manual QA remains irreplaceable Experience managing a geographically distributed team (US + India or equivalent), with the mentorship instincts and cultural fluency that requires Hands-on technical depth: Python, CI/CD (GitHub Actions, Jenkins, or equivalent), pytest or equivalent test frameworks, Docker, AWS or GCP, and familiarity with at least one of hardware-in-the-loop, robotics simulation, or ML model evaluation harnesses Pittsburgh-based or genuinely willing to relocate — this is an on-site/hybrid role and is not eligible for full remote Nice to Have Hardware QA or field reliability experience with sensors, cameras, embedded devices, drones, or robotics Experience with simulation-based testing (Gazebo, Isaac Sim, or in-house sim) for robotics or perception systems Background in warehouse, logistics, or industrial deployment environments Experience building or operating QA for a multi-tenant SaaS platform at scale", "summaryDescription" : "Director of Quality at Gather AI. Skills: Quality Assurance, AI/ML, Robotics, Cloud Platform. Own and evolve QA strategy across drone hardware,. Establish release qualification gates for full stack", "postedDate" : "2026-06-16T01:15:26.096", "createdAt" : "2026-06-16T01:15:26.096", "lastUpdated" : "2026-06-16T13:26:07.603", "ingestTimestamp" : "2026-06-16T01:15:26.096", "mongoId" : "6a306f60f292fd229cfe83b2", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 175000, "salaryAnnualMax" : 250000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Test automation", "Model evaluation", "Data pipeline validation", "Hardware-in-the-loop", "Robotics simulation", "ML model evaluation", "Leadership", "Mentoring", "Quality Assurance", "AI/ML", "Robotics", "Cloud Platform", "System design", "Release management", "Release qualification gates", "Warehouse intelligence", "Supply chain", "Computer vision", "ML models", "Cloud platform", "Embedded systems", "SaaS platform", "GitHub Actions", "Jenkins", "Docker", "AWS", "GCP", "Gazebo", "Isaac Sim" ], "skillCount" : 29, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Director", "dataQualityScore" : 1.0, "_score" : 1232.9874, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Logistics", "llmIndustryConfidence" : 0.97 }, { "id" : "6a2c5e6674d8ee00a08e3c18", "title" : "Associate Director, GCP Quality Assurance", "company" : "Beeline Medicines", "industry" : "Biotechnology", "salary" : { "min" : 165750.0, "max" : 214500.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Boston, Massachusetts, United States", "locations" : [ "Boston", "Massachusetts", "United States" ], "timestamp" : "2026-06-15T00:40:10.939", "fingerprint" : "723bba1a04c8812faf8583095edd58f8813f67215217c751bd6114e9a81b2d26", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/beelinemedicines/jobs/4266719009", "externalId" : "4266719009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Boston", "state" : "Massachusetts", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "42.3588336,-71.0578303" } ], "locationText" : "Boston, Massachusetts, United States", "experienceMinYears" : 7, "experienceLevel" : "Director", "professionalSkills" : [ "Quality Assurance", "Clinical Quality", "GCP Quality Assurance", "Clinical development", "Regulatory Affairs", "Pharmacovigilance", "Data Management", "Vendor oversight", "Risk-based quality management", "Inspection readiness" ], "hardSkillsList" : [ "GCP regulations", "Clinical trial oversight", "Regulatory inspections", "Audits", "Vendor oversight", "Risk management" ], "softSkillsList" : [ "Cross-functional collaboration", "Transparent dialogue", "Solution-oriented dialogue" ], "hardSkills" : [ { "name" : "GCP regulations", "level" : "intermediate" }, { "name" : "Clinical trial oversight", "level" : "intermediate" }, { "name" : "Regulatory inspections", "level" : "intermediate" }, { "name" : "Audits", "level" : "intermediate" }, { "name" : "Vendor oversight", "level" : "intermediate" }, { "name" : "Risk management", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Cross-functional collaboration" }, { "name" : "Transparent dialogue" }, { "name" : "Solution-oriented dialogue" } ], "majorSkills" : "GCP Quality Assurance, Clinical trial oversight, Regulatory inspections, Risk management", "majorSkillsList" : [ "GCP Quality Assurance", "Clinical trial oversight", "Regulatory inspections", "Risk management" ], "coreResponsibilities" : "Provide strategic Quality Assurance oversight, Provide operational Quality Assurance oversight, Ensure clinical trials compliance, Maintain continuous state of inspection readiness, Partner with Clinical Operations, Partner with Regulatory Affairs, Partner with Pharmacovigilance, Partner with Data Management, Partner with external service providers, Implement risk-based quality oversight model, Manage GCP quality systems, Manage vendor oversight, Manage audits, Manage inspection support, Embed quality by design", "teamCollaboration" : "Clinical Operations; Regulatory Affairs; Pharmacovigilance; Data Management; External service providers; Cross-functional teams", "domainKnowledge" : "Good Clinical Practice; GCP regulations; Clinical lifecycle", "domainList" : [ "good-clinical-practice", "gcp-regulations", "clinical-lifecycle" ], "domainSpecificKnowledge" : [ "Good Clinical Practice", "GCP regulations", "Clinical lifecycle" ], "communicationSkills" : "Proactive communication; Escalate issues", "problemSolvingSkills" : "Solution-oriented dialogue", "qualificationsBasic" : "7+ years of experience in GCP Quality Assurance, Knowledge of global GCP regulations, Knowledge of clinical trial oversight requirements, Demonstrated experience supporting regulatory inspections, Demonstrated experience supporting audits, Experience overseeing CROs, Experience overseeing GCP service providers, Experience supporting late-stage clinical trials, Experience supporting pivotal clinical trials, Background in risk-based quality management, Background in inspection readiness, Ability to balance compliance with operational execution, Commitment to patient safety, Commitment to data integrity, Commitment to quality culture", "qualificationsPreferred" : "Advanced degree preferred", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "About Beeline Medicines: Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully. Job Summary: The Associate Director, GCP Quality Assurance is responsible for providing strategic and operational Quality Assurance oversight for Good Clinical Practice (GCP) activities supporting the company’s clinical development programs. This role ensures that clinical trials are conducted in compliance with applicable regulatory requirements, company policies, and global GCP standards, with a continuous state of inspection readiness. The Director partners closely with Clinical Operations, Regulatory Affairs, Pharmacovigilance, Data Management, and external service providers to implement a risk-based quality oversight model across the clinical lifecycle. The role is accountable for GCP quality systems, vendor oversight, audits, and inspection support, and plays a critical role in embedding quality by design into clinical development programs. Work Arrangement advanced degree strongly preferred. 7+ years of experience in GCP Quality Assurance or Clinical Quality within a biotech or pharmaceutical environment. Strong knowledge of global GCP regulations and clinical trial oversight requirements. Demonstrated experience supporting regulatory inspections and audits. Experience overseeing CROs and other GCP service providers. Experience supporting late-stage or pivotal clinical trials. Strong background in risk-based quality management and inspection readiness. Ability to balance compliance with operational execution Commitment to patient safety, data integrity, and quality culture Strong cross-functional collaborator who proactively communicates quality risk, escalates issues with appropriate context and urgency, and fosters a culture of transparent, solution-oriented dialogue. Salary Range: The expected annual salary range for this position is listed below. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance. Salary Range $165,750—$214,500 USD Benefits: We offer a comprehensive benefits package including: Medical, Dental & Vision insurance (employee premiums 100% covered by company) 20 accrued days combined time off (PTO/Sick), 12 company holidays, & winter recharge Flexible work arrangements / hybrid schedule Health Savings Account (HSA) *Benefits are subject to eligibility requirements and plan terms. Additional details provided during the offer process* Equal Employment Opportunity: Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law. Reasonable Accommodation: If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates. Privacy Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at Privacy Policy - Beeline Medicines", "summaryDescription" : "Associate Director, GCP Quality Assurance at Beeline Medicines. Skills: GCP Quality Assurance, Clinical trial oversight, Regulatory inspections, Risk management. Provide strategic Quality Assurance oversight. Provide operational Quality Assurance oversight", "postedDate" : "2026-06-12T22:03:29.123", "createdAt" : "2026-06-12T22:03:29.123", "lastUpdated" : "2026-06-15T00:40:10.939", "ingestTimestamp" : "2026-06-12T22:03:29.123", "mongoId" : "6a2c5e6674d8ee00a08e3c18", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 165750, "salaryAnnualMax" : 214500, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "GCP regulations", "Clinical trial oversight", "Regulatory inspections", "Audits", "Vendor oversight", "Risk management", "Cross-functional collaboration", "Transparent dialogue", "Solution-oriented dialogue", "GCP Quality Assurance", "Quality Assurance", "Clinical Quality", "Clinical development", "Regulatory Affairs", "Pharmacovigilance", "Data Management", "Risk-based quality management", "Inspection readiness", "Good Clinical Practice", "Clinical lifecycle" ], "skillCount" : 20, "jobCategory" : "other", "jobSubcategory" : "regulatory-&-quality", "dataQualityScore" : 0.8888889, "_score" : 1113.6178, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotechnology" }, { "id" : "6a2c8d9f74d8ee00a0979788", "title" : "Director, Quality Assurance, GMP", "company" : "Xenon Pharmaceuticals", "industry" : "R&D Operations", "salary" : { "min" : 210000.0, "max" : 231800.0, "currency" : "USD", "frequency" : "Yearly" }, "location" : "Boston", "locations" : [ "Boston" ], "timestamp" : "2026-06-16T01:27:11.774", "fingerprint" : "8a5180cd84cb7b862e3821486db2f2753cec0e17fe63b25629d79a64a1402729", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/xenon/0fd257c7-e773-44c3-b378-ee7da5f9e47f/application", "externalId" : "0fd257c7-e773-44c3-b378-ee7da5f9e47f", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Boston", "state" : "Massachusetts", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "42.3588336,-71.0578303" }, { "city" : "Vancouver", "state" : "British Columbia", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "49.2608724,-123.1139520" } ], "locationText" : "Boston, Massachusetts, United States; Vancouver, British Columbia, Canada", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "professionalSkills" : [ "Quality leadership", "Drug discovery", "Clinical development", "Commercialization", "Manufacturing", "Testing", "Release", "Batch reviews", "Analytical method validations", "Tech transfers", "Deviations", "Quality agreements", "Supplier qualifications", "Auditing", "Monitoring", "CMC functions", "CGMP compliance", "Quality systems", "Audit reports", "Quality metrics", "Vendor metrics", "Health authority documents", "Data integrity", "Project teams", "Health Authority Inspections", "Operational meetings", "Quality mindset", "Quality excellence", "Total quality management", "Continuous improvement" ], "hardSkillsList" : [ "Small molecule manufacturing", "Drug substance manufacture", "Drug product manufacture", "Solid oral dosage", "Finished goods production", "Distribution" ], "softSkillsList" : [ "Leadership", "Mentoring" ], "hardSkills" : [ { "name" : "Small molecule manufacturing", "level" : "intermediate" }, { "name" : "Drug substance manufacture", "level" : "intermediate" }, { "name" : "Drug product manufacture", "level" : "intermediate" }, { "name" : "Solid oral dosage", "level" : "intermediate" }, { "name" : "Finished goods production", "level" : "intermediate" }, { "name" : "Distribution", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "Quality Assurance, GMP, Clinical programs", "majorSkillsList" : [ "Quality Assurance", "GMP", "Clinical programs" ], "coreResponsibilities" : "Manage quality-related matters for manufacturing, Manage quality-related matters for testing, Manage quality-related matters for release at CMO, Lead activities related to external quality, Support activities related to external quality, Perform batch reviews, Perform batch release, Perform analytical method validations, Perform tech transfers, Manage deviations, Manage quality agreements, Manage supplier qualifications, Conduct audits, Monitor suppliers, Collaborate with internal CMC functions, Align goals and objectives for clinical phase programs, Align goals and objectives for small molecule products, Ensure cGMP compliance, Ensure realization of value-added policies, Ensure realization of best practices, Author quality documents, Review quality documents, Approve quality documents, Author quality agreements, Review quality agreements, Approve quality agreements, Author Quality systems documents, Review Quality systems documents, Approve Quality systems documents, Author audit reports, Review audit reports, Approve audit reports, Attend CMO meetings, Attend internal CMC team meetings, Provide quality feedback supporting Xenon products, Collaborate on complex investigations, Support quality system review meetings, Support product review meetings, Provide data for quality metrics, Provide data for internal metrics, Provide data for vendor metrics, Provide quality reviews of key CMC documents, Provide quality reviews of health authority documents, Review data to assure compliance, Verify data to assure compliance, Represent Quality function on project teams, Represent Quality function on Health Authority Inspections, Represent Quality function on suppliers meetings, Represent Quality function on CMO operational meetings, Represent Quality function on QA to QA meetings, Promote a quality mindset throughout the organization, Promote quality excellence approach throughout the organization, Recruit direct reports, Lead direct reports, Direct direct reports, Develop direct reports, Coach direct reports, Evaluate direct reports", "teamCollaboration" : "R&D Operations group; Internal CMC functions; Cross functional projects; Working with suppliers; Working with CMOs", "domainKnowledge" : "Neuroscience; Ion channel biology; Human genetics; Small molecule manufacturing; Drug substance manufacture; Drug product manufacture; Solid oral dosage; Finished goods production; Distribution; Global GxP expectations; QP requirements", "domainList" : [ "neuroscience", "ion-channel-biology", "human-genetics", "small-molecule-manufacturing", "drug-substance-manufacture", "drug-product-manufacture", "solid-oral-dosage", "finished-goods-production", "distribution", "global-gxp-expectations", "qp-requirements" ], "domainSpecificKnowledge" : [ "Neuroscience", "Ion channel biology", "Human genetics", "Small molecule manufacturing", "Drug substance manufacture", "Drug product manufacture", "Solid oral dosage", "Finished goods production", "Distribution", "Global GxP expectations", "QP requirements" ], "communicationSkills" : "Proactive communication; Solution-focused communication", "documentationSkills" : "Quality documents; Quality agreements; Quality systems documents; Audit reports; CMC documents; Health authority documents", "continuousLearning" : "Training; Learning & Development program; Tuition Assistance program", "problemSolvingSkills" : "Troubleshoot problems; Resolve problems", "qualificationsBasic" : "10+ years of experience in GMP quality leadership, Degree in a life sciences discipline, Experience with small molecule manufacturing, Experience in solid oral dosage, Experience in finished goods production, Experience in distribution, Extensive GxP knowledge, Early phase drug development experience, Experience with a small virtual company, Ability to effectively organize, multitask, Ability to work in a fast-paced, deadline driven work environment, Extensive experience establishing key quality system metrics, Extensive experience establishing process indicators, Interpersonal skills, Ability to communicate in a proactive and solution-focused manner, Ability to communicate issues with CMOs, Goal oriented, Ability to troubleshoot and resolve problems, Ability to work with minimal supervision, Ability to set priorities to meet timelines, Ability to motivate and influence others, Team building skills, Managing skills", "qualificationsPreferred" : "Experience with global GxP expectations, Experience with QP requirements, Experience in leading cross functional projects, Successful track record working with suppliers, Successful track record working with CMOs, Recruiting skills, Coaching skills, Counseling skills, Disciplining skills", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Who We Are: Xenon Pharmaceuticals (NASDAQ:XENE https://www.nasdaq.com/market-activity/stocks/xene) is a neuroscience-focused biopharmaceutical company dedicated to drug discovery, clinical development, and commercialization of life-changing therapeutics for patients in need. We are looking for great people who thrive in a respectful, collaborative, inclusive, and productive culture to join the Xenon team. What We Do: We are advancing an exciting product pipeline https://xenon-pharma.com/pipeline to address indications with high unmet medical need, including epilepsy, depression and pain. Our Phase 3 azetukalner program represents the most advanced, clinically validated potassium channel modulator in late-stage clinical development for multiple indications. In March 2026, we announced positive topline data from our Phase 3 X-TOLE2 study of azetukalner in focal onset seizures (FOS), and we anticipate submitting a New Drug Application to the Food and Drug Administration in the third quarter of 2026. Our Phase 3 epilepsy program also includes a second FOS study, X-TOLE3, which would support regulatory submissions outside the U.S., and the X-ACKT study in primary generalized tonic-clonic seizures, which would support regulatory submissions for an additional epilepsy indication. We also have multiple Phase 3 azetukalner clinical trials underway in major depressive disorder (MDD) and bipolar depression (BPD), based on topline data from our Phase 2 X-NOVA clinical trial. In addition, we are proud of our strong heritage in human genetics, deep understanding of ion channel biology, and expertise in novel chemistries to enable potent, selective ion channel targeting. We continue to advance an early-stage pipeline of novel therapeutic candidates, including Phase 1 studies for XEN1701 (targeting Nav1.7) and XEN1120 (targeting Kv7), which are important pain targets. Backed by a strong balance sheet to support our growth plans, we continue to build a fully integrated, premier neuroscience company with strong discovery, clinical development, corporate, and commercial operations. We are seeking a Director, Quality Assurance, GMP focusing on clinical programs to join our team. This position will be an integral member of the Quality GMP team as well as a key member of highly collaborative R&D Operations group comprised of Program Management, CMC, Regulatory, Supply Chain and Quality functions. Leveraging an extensive background in quality and manufacturing in all clinical phases will ensure the quality program requirements are met. The successful candidate will have proven leadership ability in a fast-paced and complex environment, and will interact with all levels of internal staff, as well as external advisors and partners. This position reports to the Executive Director, Quality Assurance, GMP and will be based out of Vancouver, BC, Canada or Boston, MA, USA in our Needham office. We will consider other jurisdictions for exceptional candidates. The level of the position will be commensurate with the candidate’s education and industry experience. Relocation and immigration support will be provided, if required. This role is a hybrid position, requiring a minimum of 2 days per week in the office. RESPONSIBILITIES: · Responsible for quality-related matters related to manufacturing, testing and release at a CMO (Contract Manufacturing Organization) focusing on products in the clinical stage of development. · Lead and support activities related to external quality such as, but not limited to, batch reviews and release, analytical method validations, tech transfers, deviations, quality agreements, and supplier qualifications including auditing and monitoring. · Collaborate with internal CMC functions and aligns goals and objectives for clinical phase programs and small molecule products, ensuring cGMP compliance and realization of value-added policies and best practices. · Author and review/approve quality documents including quality agreements, dispositions, Quality systems documents, audit reports, etc.... · Attend CMO and internal CMC team meetings and provide quality feedback supporting Xenon products including collaborations on complex investigations. · Support quality system and product review meetings including providing data for quality metrics (internal and vendor metrics). Provide quality reviews of key CMC and health authority documents. Review and verify data to assure compliance with data integrity. · Represent Quality function on project teams, Health Authority Inspections, suppliers and CMO operational meetings, and QA to QA meetings. · Promote a quality mindset and quality excellence approach throughout the organization. · Recruit, lead, direct, develop, coach and evaluate direct reports, if any, in accordance with the Company’s Human Resource policies and practices. · Act in accordance with Company policies, including, for example, the Code of Business Conduct and Ethics and ensure policies are understood and followed by direct reports, if any. · Some international travel may be required. · Other duties as assigned. QUALIFICATIONS: · Bachelor’s degree in a life sciences discipline, with 10+ years of experience in GMP quality leadership positions. · Strong understanding of small molecule manufacturing including drug substance manufacture, drug product manufacture with direct experience in solid oral dosage and finished goods production and distribution. · Extensive GxP knowledge with early phase drug development experience. · Experience with a small virtual company. · Strong knowledge of global GxP expectations and QP (Qualified Person) requirements. · Ability to effectively organize, multitask, and work in a fast-paced, deadline driven work environment. · Extensive experience establishing key quality system metrics and process indicators to proactively identify and address quality systems or product issues. · Strong interpersonal skills, with experience in leading cross functional projects including a successful track record working with suppliers and CMOs. · Ability to communicate in a proactive and solution-focused manner, including keeping management aware of potential issues. Ability to communicate issues with CMOs. · Goal oriented with the ability to troubleshoot and resolve problems. · Be a champion for continuous improvement in all aspects of total quality management. · Ability to work with minimal supervision, to set priorities to meet timelines, and to motivate and influence others. · Team building and managing skills including recruiting, coaching, counseling, and disciplining. Our Total Rewards program includes base salary, target bonus, and stock options, as well as a full range of benefits including medical, dental, vision, short-& long-term disability, accidental death & dismemberment, and life insurance programs, Employee Assistance Program, travel insurance, and retirement savings programs with company matching contributions. Xenon encourages time to rest and re-charge through vacation, personal days, sick days, and an end-of-year company shutdown. Xenon highly values employee development and has an expanding Training, Learning & Development program, including a Tuition Assistance program for advanced degrees.", "summaryDescription" : "Director, Quality Assurance, GMP at Xenon Pharmaceuticals. Skills: Quality Assurance, GMP, Clinical programs. Manage quality-related matters for manufacturing. 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}, "location" : "Italy", "locations" : [ "Italy" ], "certifications" : [ "Quality assurance certifications", "Clinical research certifications", "Regulatory affairs certifications" ], "timestamp" : "2026-06-16T02:04:18.744", "fingerprint" : "5d894eccca41fc879a7a47868006a5be9d1cc10782124d028ad28b42b2ba16f5", "source" : "lever", "language" : "en", "applyUrl" : "https://jobs.lever.co/jobgether/24f7c787-b58c-418a-95a8-9192d093ccde/apply", "externalId" : "24f7c787-b58c-418a-95a8-9192d093ccde", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Germany", "continent" : "eu", "workMode" : "remote" } ], "locationText" : "Germany", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceLevel" : "Director", "technicalSkills" : "ETMF platforms", "professionalSkills" : [ "Quality Assurance", "Regulatory compliance", "Audit management", "Vendor management", "Inspection readiness", "Quality metrics", "Key performance indicators", "Remediation activities", "Quality Management System", "Cross-functional teams", "Governance forums", "Stakeholder management" ], "hardSkillsList" : [ "GCP", "GVP", "GLP", "ICH guidelines", "FDA regulations", "Pharmacovigilance regulations" ], "softSkillsList" : [ "Leadership", "Mentoring" ], "hardSkills" : [ { "name" : "GCP", "level" : "intermediate" }, { "name" : "GVP", "level" : "intermediate" }, { "name" : "GLP", "level" : "intermediate" }, { "name" : "ICH guidelines", "level" : "intermediate" }, { "name" : "FDA regulations", "level" : "intermediate" }, { "name" : "Pharmacovigilance regulations", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "GCP Quality Assurance, Regulatory Inspections, Quality Management System", "majorSkillsList" : [ "GCP Quality Assurance", "Regulatory Inspections", "Quality Management System" ], "coreResponsibilities" : "Lead and oversee GCP quality activities, Ensure studies are compliant with regulations, Ensure studies are compliant with ICH guidelines, Ensure studies are compliant with internal procedures, Serve as primary quality partner for clinical operations, Support protocol review, Support execution activities, Support reporting activities, Support continuous inspection readiness, Manage quality oversight of external CROs, Manage quality oversight of vendors, Manage quality oversight of strategic partners, Ensure alignment on quality standards, Ensure alignment on issue escalation processes, Ensure alignment on audit outcomes, Ensure alignment on corrective actions, Direct inspection readiness initiatives, Support regulatory authority inspections, Coordinate responses to inspections, Manage observation management, Follow-up on regulatory commitments, Maintain oversight of eTMF quality, Maintain oversight of protocol deviations, Maintain oversight of non-conformances, Maintain oversight of CAPA management, Maintain oversight of quality metrics, Maintain oversight of key performance indicators, Lead audits of clinical sites, Lead audits of vendors, Lead audits of service providers, Support audits of clinical sites, Support audits of vendors, Support audits of service providers, Review audit findings, Ensure effective remediation activities, Provide quality expertise for pharmacovigilance activities, Provide quality oversight for pharmacovigilance activities, Provide quality expertise for pre-clinical activities, Provide quality oversight for pre-clinical activities, Ensure compliance with GVP regulations, Ensure compliance with GLP regulations, Ensure compliance with industry standards, Contribute to QMS development, Contribute to QMS continuous improvement, Develop SOPs, Develop training programs, Develop quality events, Develop regulatory intelligence activities, Represent Quality Assurance within cross-functional teams, Represent Quality Assurance within governance forums, Promote a culture where quality supports business objectives, Promote a culture where quality supports clinical objectives, Mentor quality team members, Develop quality team members, Provide leadership across the organization, Provide guidance across the organization", "teamCollaboration" : "Cross-functional teams; Governance forums", "projectManagementSkills" : [ "Quality Management System" ], "domainKnowledge" : "GCP; GVP; GLP; ICH standards; FDA regulations; EU Clinical Trial requirements; Pharmacovigilance regulations; GLP principles; Clinical development programs; Neurology; Neurodegenerative diseases; Rare diseases", "domainList" : [ "gcp", "gvp", "glp", "ich-standards", "fda-regulations", "eu-clinical-trial-requirements", "pharmacovigilance-regulations", "glp-principles", "clinical-development-programs", "neurology", "neurodegenerative-diseases", "rare-diseases" ], "domainSpecificKnowledge" : [ "GCP", "GVP", "GLP", "ICH standards", "FDA regulations", "EU Clinical Trial requirements", "Pharmacovigilance regulations", "GLP principles", "Clinical development programs", "Neurology", "Neurodegenerative diseases", "Rare diseases" ], "toolProficiency" : [ "Electronic quality systems", "ETMF platforms" ], "communicationSkills" : "Translate regulatory requirements", "continuousLearning" : "Professional development; Leadership growth opportunities", "specialRequirements" : "Occasional international travel", "qualificationsBasic" : "Bachelor’s degree or higher in Life Sciences, Pharmacy, or related, Extensive experience in GCP Quality Assurance, Leadership experience at Director level or equivalent, Expertise across GCP, GVP, and GLP quality frameworks, Hands-on experience planning, conducting, and managing audits, Deep understanding of international regulatory requirements, Proven track record supporting or leading successful regulatory inspections, Experience managing interactions with global health authorities, Experience establishing, enhancing, or maintaining quality management systems, Proficiency with electronic quality systems, Proficiency with eTMF platforms, Proficiency with quality documentation processes, Excellent communication skills, Excellent stakeholder management skills", "qualificationsPreferred" : "Advanced scientific or healthcare qualifications preferred, Experience within neurology, neurodegenerative diseases, rare diseases, Experience within advanced clinical development programs, Familiarity with risk-based quality approaches, Familiarity with centralized monitoring methodologies, Familiarity with modern clinical quality strategies, Relevant professional certifications in quality assurance, Relevant professional certifications in clinical research, Relevant professional certifications in regulatory affairs", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "## Accountabilities Lead and oversee GCP quality activities across global clinical development programs, ensuring studies are conducted, documented, and reported in compliance with applicable regulations, ICH guidelines, and internal procedures. Serve as the primary quality partner for clinical operations from study startup through study completion, supporting protocol review, execution, reporting activities, and continuous inspection readiness. Manage quality oversight of external CROs, vendors, and strategic partners, ensuring alignment on quality standards, issue escalation processes, audit outcomes, and corrective actions. Direct inspection readiness initiatives and support regulatory authority inspections, coordinating responses, observation management, and regulatory commitment follow-up. Maintain oversight of eTMF quality, protocol deviations, non-conformances, CAPA management, quality metrics, and key performance indicators. Lead or support audits of clinical sites, vendors, and service providers while reviewing audit findings and ensuring effective remediation activities. Provide quality expertise and oversight for pharmacovigilance and pre-clinical activities, ensuring compliance with relevant GVP and GLP regulations and industry standards. Contribute to the development and continuous improvement of the Quality Management System (QMS), including SOPs, training programs, quality events, and regulatory intelligence activities. Represent Quality Assurance within cross-functional teams and governance forums, promoting a culture where quality supports business and clinical objectives. Mentor and develop quality team members while providing leadership and guidance across the organization. Requirements Bachelor’s degree or higher in Life Sciences, Pharmacy, or a related field; advanced scientific or healthcare qualifications are preferred. Extensive experience in GCP Quality Assurance within pharmaceutical, biotechnology, or CRO environments, including leadership experience at Director level or equivalent. Strong expertise across GCP, GVP, and GLP quality frameworks, with hands-on experience planning, conducting, and managing audits. Deep understanding of international regulatory requirements and guidelines, including ICH standards, FDA regulations, EU Clinical Trial requirements, pharmacovigilance regulations, and GLP principles. Proven track record supporting or leading successful regulatory inspections and managing interactions with global health authorities. Experience establishing, enhancing, or maintaining quality management systems within growing or mid-sized life sciences organizations. Proficiency with electronic quality systems, eTMF platforms, and quality documentation processes. Excellent communication and stakeholder management skills, with the ability to translate complex regulatory requirements into practical guidance. Highly autonomous, proactive, organized, and capable of operating effectively in a dynamic, resource-conscious environment. Experience within neurology, neurodegenerative diseases, rare diseases, or advanced clinical development programs is advantageous. Familiarity with risk-based quality approaches, centralized monitoring methodologies, and modern clinical quality strategies is considered a plus. Relevant professional certifications in quality assurance, clinical research, or regulatory affairs are desirable. Benefits Competitive senior-level compensation package. Fully remote work environment within Germany. Flexible working schedule with international collaboration across multiple time zones. Opportunity to play a key role in late-stage global clinical development programs. Exposure to cross-functional leadership and strategic decision-making. International and collaborative work environment. Professional development and leadership growth opportunities. Occasional international travel for business, audits, inspections, and stakeholder meetings. Meaningful work supporting the development of innovative treatments for serious and underserved medical conditions. ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Director / Senior Director, GCP Quality Assurance Lead. Skills: GCP Quality Assurance, Regulatory Inspections, Quality Management System. Lead and oversee GCP quality activities. 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Mentoring", "Team Development", "Leadership Guidance" ], "hardSkillsList" : [ "ICH guidelines", "FDA regulations", "Pharmacovigilance regulations", "GLP principles" ], "hardSkills" : [ { "name" : "ICH guidelines", "level" : "intermediate" }, { "name" : "FDA regulations", "level" : "intermediate" }, { "name" : "Pharmacovigilance regulations", "level" : "intermediate" }, { "name" : "GLP principles", "level" : "intermediate" } ], "majorSkills" : "GCP Quality Assurance, Regulatory Inspections, Quality Management System", "majorSkillsList" : [ "GCP Quality Assurance", "Regulatory Inspections", "Quality Management System" ], "coreResponsibilities" : "Lead GCP quality activities, Oversee GCP quality activities, Ensure studies compliance, Ensure studies documentation, Ensure studies reporting, Serve as quality partner, Support protocol review, Support execution activities, Support reporting activities, Support continuous inspection readiness, Manage quality oversight of CROs, Manage quality oversight of vendors, Manage quality oversight of partners, Ensure alignment on quality standards, Ensure alignment on issue escalation, Ensure alignment on audit outcomes, Ensure alignment on corrective actions, Direct inspection readiness initiatives, Support regulatory authority inspections, Coordinate responses to inspections, Manage observation management, Follow-up on regulatory commitments, Maintain oversight of eTMF quality, Maintain oversight of protocol deviations, Maintain oversight of non-conformances, Maintain oversight of CAPA management, Maintain oversight of quality metrics, Maintain oversight of key performance indicators, Lead audits of clinical sites, Lead audits of vendors, Lead audits of service providers, Support audits of clinical sites, Support audits of vendors, Support audits of service providers, Review audit findings, Ensure effective remediation activities, Provide quality expertise for pharmacovigilance, Provide quality oversight for pharmacovigilance, Provide quality expertise for pre-clinical activities, Provide quality oversight for pre-clinical activities, Contribute to QMS development, Contribute to QMS continuous improvement, Represent Quality Assurance in teams, Represent Quality Assurance in forums, Promote quality culture, Mentor quality team members, Develop quality team members, Provide leadership across organization, Provide guidance across organization", "teamCollaboration" : "Cross-functional teams; Governance forums", "domainKnowledge" : "GCP; GVP; GLP; ICH standards; FDA regulations; EU Clinical Trial requirements; Pharmacovigilance regulations; GLP principles; Neurology; Neurodegenerative diseases; Rare diseases; Clinical development programs", "domainList" : [ "gcp", "gvp", "glp", "ich-standards", "fda-regulations", "eu-clinical-trial-requirements", "pharmacovigilance-regulations", "glp-principles", "neurology", "neurodegenerative-diseases", "rare-diseases", "clinical-development-programs" ], "domainSpecificKnowledge" : [ "GCP", "GVP", "GLP", "ICH standards", "FDA regulations", "EU Clinical Trial requirements", "Pharmacovigilance regulations", "GLP principles", "Neurology", "Neurodegenerative diseases", "Rare diseases", "Clinical development programs" ], "toolProficiency" : [ "Electronic quality systems", "ETMF platforms" ], "communicationSkills" : "Translate regulatory requirements", "documentationSkills" : "ICH guidelines; FDA regulations; EU Clinical Trial requirements; Pharmacovigilance regulations; GLP principles", "continuousLearning" : "Professional development; Leadership growth opportunities", "specialRequirements" : "Occasional international travel", "qualificationsBasic" : "Bachelor's degree or higher, Extensive experience in GCP Quality Assurance, Leadership experience at Director level, Hands-on experience planning audits, Hands-on experience conducting audits, Hands-on experience managing audits, Deep understanding of international regulatory requirements, Proven track record supporting regulatory inspections, Proven track record leading regulatory inspections, Experience managing interactions with global health authorities, Experience establishing quality management systems, Experience enhancing quality management systems, Experience maintaining quality management systems, Proficiency with electronic quality systems, Proficiency with eTMF platforms, Proficiency with quality documentation processes, Excellent communication skills, Excellent stakeholder management skills, Highly autonomous, Proactive, Organized, Capable of operating effectively in dynamic environment, Capable of operating effectively in resource-conscious environment", "qualificationsPreferred" : "Life Sciences degree preferred, Pharmacy degree preferred, Related advanced scientific qualifications preferred, Related healthcare qualifications preferred, Experience within neurology, Experience within neurodegenerative diseases, Experience within rare diseases, Experience within advanced clinical development programs, Familiarity with risk-based quality approaches, Familiarity with centralized monitoring methodologies, Familiarity with modern clinical quality strategies, Relevant professional certifications", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "## Accountabilities Lead and oversee GCP quality activities across global clinical development programs, ensuring studies are conducted, documented, and reported in compliance with applicable regulations, ICH guidelines, and internal procedures. Serve as the primary quality partner for clinical operations from study startup through study completion, supporting protocol review, execution, reporting activities, and continuous inspection readiness. Manage quality oversight of external CROs, vendors, and strategic partners, ensuring alignment on quality standards, issue escalation processes, audit outcomes, and corrective actions. Direct inspection readiness initiatives and support regulatory authority inspections, coordinating responses, observation management, and regulatory commitment follow-up. Maintain oversight of eTMF quality, protocol deviations, non-conformances, CAPA management, quality metrics, and key performance indicators. Lead or support audits of clinical sites, vendors, and service providers while reviewing audit findings and ensuring effective remediation activities. Provide quality expertise and oversight for pharmacovigilance and pre-clinical activities, ensuring compliance with relevant GVP and GLP regulations and industry standards. Contribute to the development and continuous improvement of the Quality Management System (QMS), including SOPs, training programs, quality events, and regulatory intelligence activities. Represent Quality Assurance within cross-functional teams and governance forums, promoting a culture where quality supports business and clinical objectives. Mentor and develop quality team members while providing leadership and guidance across the organization. Requirements Bachelor’s degree or higher in Life Sciences, Pharmacy, or a related field; advanced scientific or healthcare qualifications are preferred. Extensive experience in GCP Quality Assurance within pharmaceutical, biotechnology, or CRO environments, including leadership experience at Director level or equivalent. Strong expertise across GCP, GVP, and GLP quality frameworks, with hands-on experience planning, conducting, and managing audits. Deep understanding of international regulatory requirements and guidelines, including ICH standards, FDA regulations, EU Clinical Trial requirements, pharmacovigilance regulations, and GLP principles. Proven track record supporting or leading successful regulatory inspections and managing interactions with global health authorities. Experience establishing, enhancing, or maintaining quality management systems within growing or mid-sized life sciences organizations. Proficiency with electronic quality systems, eTMF platforms, and quality documentation processes. Excellent communication and stakeholder management skills, with the ability to translate complex regulatory requirements into practical guidance. Highly autonomous, proactive, organized, and capable of operating effectively in a dynamic, resource-conscious environment. Experience within neurology, neurodegenerative diseases, rare diseases, or advanced clinical development programs is advantageous. Familiarity with risk-based quality approaches, centralized monitoring methodologies, and modern clinical quality strategies is considered a plus. Relevant professional certifications in quality assurance, clinical research, or regulatory affairs are desirable. Benefits Competitive senior-level compensation package. Fully remote work environment within Germany. Flexible working schedule with international collaboration across multiple time zones. Opportunity to play a key role in late-stage global clinical development programs. Exposure to cross-functional leadership and strategic decision-making. International and collaborative work environment. Professional development and leadership growth opportunities. Occasional international travel for business, audits, inspections, and stakeholder meetings. Meaningful work supporting the development of innovative treatments for serious and underserved medical conditions. ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Director / Senior Director, GCP Quality Assurance Lead. Skills: GCP Quality Assurance, Regulatory Inspections, Quality Management System. Lead GCP quality activities. Oversee GCP quality activities", "postedDate" : "2026-06-10T04:30:24.050", "createdAt" : "2026-06-10T04:30:24.050", "lastUpdated" : "2026-06-16T04:31:10.961", "ingestTimestamp" : "2026-06-14T21:38:25.624", "mongoId" : "6a2cb20a74d8ee00a09df1bb", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "ICH guidelines", "FDA regulations", "Pharmacovigilance regulations", "GLP principles", "GCP Quality Assurance", "Regulatory Inspections", "Quality Management System", "Quality Assurance", "Clinical Development", "Regulatory Compliance", "Audit Management", "Vendor Management", "Inspection Readiness", "CAPA Management", "Quality Metrics", "Key Performance Indicators", "Pharmacovigilance Oversight", "Pre-clinical Oversight", "SOP Development", "Training Program Development", "Regulatory Intelligence", "Cross-functional Teams", "Stakeholder Management", "Team Mentoring", "Team Development", "Leadership Guidance", "GCP", "GVP", "GLP", "ICH standards", "EU Clinical Trial requirements", "Neurology", "Neurodegenerative diseases", "Rare diseases", "Clinical development programs", "Electronic quality systems", "ETMF platforms" ], "skillCount" : 37, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 993.30133, "daysOld" : 6, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.97 }, { "id" : "6a2cb20a74d8ee00a09df1b3", "title" : "Director / Senior Director, GCP Quality Assurance Lead", "industry" : "Others", "salary" : { "min" : 135000.0, "max" : 195000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Director, GCP Quality Assurance Lead in Germany, adjusted for seniority and industry." }, "location" : "France", "locations" : [ "France" ], "certifications" : [ "Quality assurance certifications", "Clinical research certifications", "Regulatory affairs certifications" ], "timestamp" : "2026-06-16T02:54:12.706", "fingerprint" : "e5690933ac88253845ad661ba5aaea880f1ab919a7762b09deb8de78ca59d67f", "source" : "lever", "language" : "en", "applyUrl" : "https://jobs.lever.co/jobgether/0b613fab-1a01-4932-b18e-07b3df45bfff/apply", "externalId" : "0b613fab-1a01-4932-b18e-07b3df45bfff", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Germany", "continent" : "eu", "workMode" : "remote" } ], "locationText" : "Germany", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceLevel" : "Director", "technicalSkills" : "GCP", "professionalSkills" : [ "Quality Assurance", "Stakeholder management", "Regulatory requirements" ], "hardSkillsList" : [ "Audit planning", "Audit management", "CAPA management", "Quality metrics" ], "hardSkills" : [ { "name" : "Audit planning", "level" : "intermediate" }, { "name" : "Audit management", "level" : "intermediate" }, { "name" : "CAPA management", "level" : "intermediate" }, { "name" : "Quality metrics", "level" : "intermediate" } ], "majorSkills" : "GCP Quality Assurance, Regulatory inspections, Quality Management System", "majorSkillsList" : [ "GCP Quality Assurance", "Regulatory inspections", "Quality Management System" ], "coreResponsibilities" : "Lead GCP quality activities, Ensure study compliance, Serve as quality partner, Support protocol review, Manage quality oversight, Ensure alignment on standards, Direct inspection readiness, Support regulatory inspections, Coordinate responses, Maintain oversight of eTMF, Maintain oversight of protocol deviations, Maintain oversight of non-conformances, Maintain oversight of CAPA, Maintain oversight of quality metrics, Maintain oversight of KPIs, Lead audits, Support audits, Review audit findings, Ensure remediation activities, Provide quality expertise, Provide quality oversight, Contribute to QMS development, Contribute to QMS improvement, Represent Quality Assurance, Promote quality culture, Mentor quality team members, Develop quality team members, Provide leadership, Provide guidance", "teamCollaboration" : "Cross-functional teams; Governance forums", "domainKnowledge" : "GCP; GVP; GLP; ICH guidelines; FDA regulations; EU Clinical Trial requirements; Pharmacovigilance regulations; GLP principles; Neurology; Neurodegenerative diseases; Rare diseases; Clinical development programs; Risk-based quality; Centralized monitoring", "domainList" : [ "gcp", "gvp", "glp", "ich-guidelines", "fda-regulations", "eu-clinical-trial-requirements", "pharmacovigilance-regulations", "glp-principles", "neurology", "neurodegenerative-diseases", "rare-diseases", "clinical-development-programs", "risk-based-quality", "centralized-monitoring" ], "domainSpecificKnowledge" : [ "GCP", "GVP", "GLP", "ICH guidelines", "FDA regulations", "EU Clinical Trial requirements", "Pharmacovigilance regulations", "GLP principles", "Neurology", "Neurodegenerative diseases", "Rare diseases", "Clinical development programs", "Risk-based quality", "Centralized monitoring" ], "toolProficiency" : [ "ETMF platforms", "Electronic quality systems" ], "communicationSkills" : "Translate requirements", "continuousLearning" : "Professional development; Leadership growth", "specialRequirements" : "Occasional international travel", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "## Accountabilities Lead and oversee GCP quality activities across global clinical development programs, ensuring studies are conducted, documented, and reported in compliance with applicable regulations, ICH guidelines, and internal procedures. Serve as the primary quality partner for clinical operations from study startup through study completion, supporting protocol review, execution, reporting activities, and continuous inspection readiness. Manage quality oversight of external CROs, vendors, and strategic partners, ensuring alignment on quality standards, issue escalation processes, audit outcomes, and corrective actions. Direct inspection readiness initiatives and support regulatory authority inspections, coordinating responses, observation management, and regulatory commitment follow-up. Maintain oversight of eTMF quality, protocol deviations, non-conformances, CAPA management, quality metrics, and key performance indicators. Lead or support audits of clinical sites, vendors, and service providers while reviewing audit findings and ensuring effective remediation activities. Provide quality expertise and oversight for pharmacovigilance and pre-clinical activities, ensuring compliance with relevant GVP and GLP regulations and industry standards. Contribute to the development and continuous improvement of the Quality Management System (QMS), including SOPs, training programs, quality events, and regulatory intelligence activities. Represent Quality Assurance within cross-functional teams and governance forums, promoting a culture where quality supports business and clinical objectives. Mentor and develop quality team members while providing leadership and guidance across the organization. Requirements Bachelor’s degree or higher in Life Sciences, Pharmacy, or a related field; advanced scientific or healthcare qualifications are preferred. Extensive experience in GCP Quality Assurance within pharmaceutical, biotechnology, or CRO environments, including leadership experience at Director level or equivalent. Strong expertise across GCP, GVP, and GLP quality frameworks, with hands-on experience planning, conducting, and managing audits. Deep understanding of international regulatory requirements and guidelines, including ICH standards, FDA regulations, EU Clinical Trial requirements, pharmacovigilance regulations, and GLP principles. Proven track record supporting or leading successful regulatory inspections and managing interactions with global health authorities. Experience establishing, enhancing, or maintaining quality management systems within growing or mid-sized life sciences organizations. Proficiency with electronic quality systems, eTMF platforms, and quality documentation processes. Excellent communication and stakeholder management skills, with the ability to translate complex regulatory requirements into practical guidance. Highly autonomous, proactive, organized, and capable of operating effectively in a dynamic, resource-conscious environment. Experience within neurology, neurodegenerative diseases, rare diseases, or advanced clinical development programs is advantageous. Familiarity with risk-based quality approaches, centralized monitoring methodologies, and modern clinical quality strategies is considered a plus. Relevant professional certifications in quality assurance, clinical research, or regulatory affairs are desirable. Benefits Competitive senior-level compensation package. Fully remote work environment within Germany. Flexible working schedule with international collaboration across multiple time zones. Opportunity to play a key role in late-stage global clinical development programs. Exposure to cross-functional leadership and strategic decision-making. International and collaborative work environment. Professional development and leadership growth opportunities. Occasional international travel for business, audits, inspections, and stakeholder meetings. Meaningful work supporting the development of innovative treatments for serious and underserved medical conditions. ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Director / Senior Director, GCP Quality Assurance Lead. Skills: GCP Quality Assurance, Regulatory inspections, Quality Management System. Lead GCP quality activities. Ensure study compliance", "postedDate" : "2026-06-10T04:30:39.883", "createdAt" : "2026-06-10T04:30:39.883", "lastUpdated" : "2026-06-16T02:54:12.706", "ingestTimestamp" : "2026-06-14T21:07:43.493", "mongoId" : "6a2cb20a74d8ee00a09df1b3", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "Audit planning", "Audit management", "CAPA management", "Quality metrics", "GCP Quality Assurance", "Regulatory inspections", "Quality Management System", "Quality Assurance", "Stakeholder management", "Regulatory requirements", "GCP", "GVP", "GLP", "ICH guidelines", "FDA regulations", "EU Clinical Trial requirements", "Pharmacovigilance regulations", "GLP principles", "Neurology", "Neurodegenerative diseases", "Rare diseases", "Clinical development programs", "Risk-based quality", "Centralized monitoring", "Quality assurance certifications", "Clinical research certifications", "Regulatory affairs certifications", "ETMF platforms", "Electronic quality systems" ], "skillCount" : 29, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 992.15796, "daysOld" : 5, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c6af174d8ee00a090f535", "title" : "Quality Assurance Director, Legal & Compliance", "company" : "Bybit", "industry" : "FinTech", "salary" : { "min" : 600000.0, "max" : 900000.0, "currency" : "AED", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Director of Quality Assurance, Legal & Compliance in Abu Dhabi, UAE, adjusted for the FinTech industry and Bybit's company profile." }, "location" : "Abu Dhabi", "locations" : [ "Abu Dhabi" ], "timestamp" : "2026-06-16T06:16:20.337", "fingerprint" : "2128e924956a2195483d261357f91bb46c9d04ee26cb2add761a0c7ba0db313d", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.eu.greenhouse.io/bybit/jobs/4878045101", "externalId" : "4878045101", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Abu Dhabi", "country" : "United Arab Emirates", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "24.4538352,54.3774014" } ], "locationText" : "Abu Dhabi, United Arab Emirates", "employmentType" : "FULL_TIME", "experienceMinYears" : 8, "experienceMaxYears" : 12, "experienceLevel" : "Director", "professionalSkills" : [ "Risk management", "Quality assurance", "Audit", "Compliance", "Stakeholder management" ], "hardSkillsList" : [ "QA reviews", "Assurance testing", "Control reviews", "Case quality assessments" ], "hardSkills" : [ { "name" : "QA reviews", "level" : "intermediate" }, { "name" : "Assurance testing", "level" : "intermediate" }, { "name" : "Control reviews", "level" : "intermediate" }, { "name" : "Case quality assessments", "level" : "intermediate" } ], "majorSkills" : "Compliance assurance, QA frameworks, Risk identification, Process improvement", "majorSkillsList" : [ "Compliance assurance", "QA frameworks", "Risk identification", "Process improvement" ], "coreResponsibilities" : "Serve as functional owner for compliance quality assurance, Act as central point for QA standards, Conduct quality reviews of compliance work, Provide oversight to QA resources, Establish QA frameworks, Design compliance assurance capability, Identify quality gaps, Partner closely with compliance teams, Produce management reporting on QA findings, Recommend process improvements, Act as quality challenger", "teamCollaboration" : "Partner with Compliance; Partner with AML; Partner with KYC/KYB; Partner with Operations", "domainKnowledge" : "AML; KYC; KYB; Transaction monitoring", "domainList" : [ "aml", "kyc", "kyb", "transaction-monitoring" ], "domainSpecificKnowledge" : [ "AML", "KYC", "KYB", "Transaction monitoring" ], "continuousLearning" : "Study Growth Fund", "problemSolvingSkills" : "Identify risks; Challenge decision-making; Drive remediation", "qualificationsBasic" : "8-12 years experience in compliance, assurance, QA, audit, AML controls, or operational risk, Hands-on experience conducting QA reviews, assurance testing, control reviews, or case quality assessments, Understanding of compliance operations and control environments, Experience designing or maturing QA or assurance frameworks, Ability to identify risks, Ability to challenge decision-making, Ability to drive remediation, Comfortable operating as an individual owner of a function, Analytical skills, Reporting skills", "workSiteFlexibility" : "Onsite", "rawDescription" : "About Us Established in 2018, Bybit is one of the world’s leading cryptocurrency exchanges and digital financial platforms, serving over 80 million users across more than 200 countries and regions. Powered by world-class technology and a user-first mindset, Bybit delivers a seamless ecosystem across trading, payments, wealth management, custody, institutional services, and Web3 — connecting users to the future of digital finance. Our core values define how we build. We listen, care and improve to create products and experiences that put users first. Backed by a global team of ambitious builders, problem-solvers, and innovators, we foster a high-performance and fast-moving environment where talent is empowered to drive real impact at the global scale. Supported by 24/7 multilingual customer service and a strong commitment to innovation, we are shaping the future of finance through technology, collaboration, and bold execution. Today, Bybit is recognized as one of the most trusted and transparent platforms in the digital asset industry, continuing to expand its global presence while building the infrastructure for the next generation of financial services. Key Responsibilities Serve as the functional owner for compliance quality assurance across the legal & compliance department Act as the central point of accountability for QA standards, review methodologies, and assurance governance Conduct hands-on quality reviews of compliance work, including case reviews, decision assessments, and process quality checks Provide oversight, direction, and calibration support to existing QA resources to ensure consistency in review standards Establish QA frameworks, scoring methodologies, review criteria, escalation standards, and reporting mechanisms Design and progressively build a broader compliance assurance capability beyond current local QA activities Identify recurring quality gaps, control weaknesses, process failures, and execution risks through thematic reviews Partner closely with Compliance, AML, KYC/KYB, Operations, and control teams to strengthen execution standards Produce management reporting on QA findings, trends, recurring issues, and assurance outcomes Recommend process, control, and training improvements based on observed findings Act as a quality challenger to drive higher operational and compliance standards across the function Requirements 8–12 years of experience in compliance, compliance assurance, QA, audit, AML controls, or operational risk within financial services, fintech, payments, or crypto Strong hands-on experience conducting QA reviews, assurance testing, control reviews, or case quality assessments Strong understanding of compliance operations and control environments, particularly within AML / KYC / onboarding / transaction monitoring environments Experience designing or maturing QA or assurance frameworks Ability to independently identify risks, challenge decision-making, and drive remediation Comfortable operating as an individual owner of a function rather than within a heavily structured team Strong analytical, reporting, and stakeholder management skills Highly detail-oriented, pragmatic, and execution-focused Why Join Us At Bybit, we are committed to fostering a supportive and enriching work environment. Our benefits include: - Study Growth Fund: We support your professional development and continuous learning. - Internal Events: Participate in regular team-building activities, workshops, and events designed to promote collaboration and innovation. - Global Collaboration: Be part of a diverse, international team, working alongside colleagues from around the world. - Career Advancement: Access opportunities for growth and advancement within a rapidly expanding global company. - Internal Mobility: Grow with us- Your long-term development is important to us. We offer internal job opportunities to help build your career path.", "summaryDescription" : "Quality Assurance Director, Legal & Compliance at Bybit. Skills: Compliance assurance, QA frameworks, Risk identification, Process improvement. Serve as functional owner for compliance quality assurance. 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"title" : "Director / Senior Director, GCP Quality Assurance Lead", "industry" : "Others", "salary" : { "min" : 180000.0, "max" : 270000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for Director level in Biotech in Romania, adjusted for seniority and industry." }, "location" : "Romania", "locations" : [ "Romania" ], "certifications" : [ "Professional certifications in quality assurance", "Professional certifications in clinical research", "Professional certifications in regulatory affairs" ], "timestamp" : "2026-06-16T05:37:51.177", "fingerprint" : "00802ea8a38376148c20ee3630f28f2ab8d4fa6bd70f9bac516d1daec06d22d6", "source" : "lever", "language" : "en", "applyUrl" : "https://jobs.lever.co/jobgether/13768128-33a3-4c16-8e25-15d21e6c16d7/apply", "externalId" : "13768128-33a3-4c16-8e25-15d21e6c16d7", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Romania", "continent" : "eu", "workMode" : "onsite" } ], "locationText" : "Romania", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceLevel" : "Director", "technicalSkills" : "GCP, ETMF", "professionalSkills" : [ "Quality Assurance", "Clinical Development", "Regulatory Compliance", "Audit Management", "Vendor Management", "Inspection Readiness", "Quality Management", "Stakeholder Management", "Team Mentoring", "Team Development" ], "hardSkillsList" : [ "GCP Quality Assurance", "GVP Quality Assurance", "GLP Quality Assurance", "ICH guidelines", "Protocol Review", "Protocol Deviations", "Non-conformances", "CAPA Management", "Quality Metrics", "Key Performance Indicators", "Pharmacovigilance Oversight", "Pre-clinical Oversight", "Regulatory Intelligence" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "GCP Quality Assurance", "level" : "intermediate" }, { "name" : "GVP Quality Assurance", "level" : "intermediate" }, { "name" : "GLP Quality Assurance", "level" : "intermediate" }, { "name" : "ICH 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Support audits of clinical sites, Support audits of vendors, Support audits of service providers, Review audit findings, Ensure effective remediation activities, Provide quality expertise for PV, Provide quality oversight for PV, Provide quality expertise for pre-clinical, Provide quality oversight for pre-clinical, Contribute to QMS development, Contribute to QMS improvement, Represent Quality Assurance in teams, Represent Quality Assurance in forums, Promote quality culture, Mentor quality team members, Develop quality team members, Provide leadership across organization, Provide guidance across organization", "teamCollaboration" : "Cross-functional teams; Governance forums", "domainKnowledge" : "GCP; GVP; GLP; ICH standards; FDA regulations; EU Clinical Trial requirements; Pharmacovigilance regulations; GLP principles; Clinical development programs; Neurology; Neurodegenerative diseases; Rare diseases", "domainList" : [ "gcp", "gvp", "glp", "ich-standards", "fda-regulations", 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inspections, Proven track record leading inspections, Managing interactions with global health authorities, Experience establishing quality management systems, Experience enhancing quality management systems, Experience maintaining quality management systems, Proficiency with electronic quality systems, Proficiency with eTMF platforms, Proficiency with quality documentation processes, Excellent communication skills, Excellent stakeholder management skills, Highly autonomous, Proactive, Organized, Capable of operating in dynamic environment, Capable of operating in resource-conscious environment", "qualificationsPreferred" : "Life Sciences degree preferred, Pharmacy degree preferred, Related advanced scientific qualifications preferred, Related healthcare qualifications preferred, Experience within neurology advantageous, Experience within neurodegenerative diseases advantageous, Experience within rare diseases advantageous, Experience within advanced clinical development programs advantageous, Familiarity with risk-based quality approaches, Familiarity with centralized monitoring methodologies, Familiarity with modern clinical quality strategies", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "## Accountabilities Lead and oversee GCP quality activities across global clinical development programs, ensuring studies are conducted, documented, and reported in compliance with applicable regulations, ICH guidelines, and internal procedures. Serve as the primary quality partner for clinical operations from study startup through study completion, supporting protocol review, execution, reporting activities, and continuous inspection readiness. Manage quality oversight of external CROs, vendors, and strategic partners, ensuring alignment on quality standards, issue escalation processes, audit outcomes, and corrective actions. Direct inspection readiness initiatives and support regulatory authority inspections, coordinating responses, observation management, and regulatory commitment follow-up. Maintain oversight of eTMF quality, protocol deviations, non-conformances, CAPA management, quality metrics, and key performance indicators. Lead or support audits of clinical sites, vendors, and service providers while reviewing audit findings and ensuring effective remediation activities. Provide quality expertise and oversight for pharmacovigilance and pre-clinical activities, ensuring compliance with relevant GVP and GLP regulations and industry standards. Contribute to the development and continuous improvement of the Quality Management System (QMS), including SOPs, training programs, quality events, and regulatory intelligence activities. Represent Quality Assurance within cross-functional teams and governance forums, promoting a culture where quality supports business and clinical objectives. Mentor and develop quality team members while providing leadership and guidance across the organization. Requirements Bachelor’s degree or higher in Life Sciences, Pharmacy, or a related field; advanced scientific or healthcare qualifications are preferred. Extensive experience in GCP Quality Assurance within pharmaceutical, biotechnology, or CRO environments, including leadership experience at Director level or equivalent. Strong expertise across GCP, GVP, and GLP quality frameworks, with hands-on experience planning, conducting, and managing audits. Deep understanding of international regulatory requirements and guidelines, including ICH standards, FDA regulations, EU Clinical Trial requirements, pharmacovigilance regulations, and GLP principles. Proven track record supporting or leading successful regulatory inspections and managing interactions with global health authorities. Experience establishing, enhancing, or maintaining quality management systems within growing or mid-sized life sciences organizations. Proficiency with electronic quality systems, eTMF platforms, and quality documentation processes. Excellent communication and stakeholder management skills, with the ability to translate complex regulatory requirements into practical guidance. Highly autonomous, proactive, organized, and capable of operating effectively in a dynamic, resource-conscious environment. Experience within neurology, neurodegenerative diseases, rare diseases, or advanced clinical development programs is advantageous. Familiarity with risk-based quality approaches, centralized monitoring methodologies, and modern clinical quality strategies is considered a plus. Relevant professional certifications in quality assurance, clinical research, or regulatory affairs are desirable. Benefits Competitive senior-level compensation package. Fully remote work environment within Germany. Flexible working schedule with international collaboration across multiple time zones. Opportunity to play a key role in late-stage global clinical development programs. Exposure to cross-functional leadership and strategic decision-making. International and collaborative work environment. Professional development and leadership growth opportunities. Occasional international travel for business, audits, inspections, and stakeholder meetings. Meaningful work supporting the development of innovative treatments for serious and underserved medical conditions. ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Director / Senior Director, GCP Quality Assurance Lead. Skills: GCP Quality Assurance, Regulatory Compliance, Audit Management, Quality Management System. Lead GCP quality activities. 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Internal CMC functions; Cross-functional projects; External advisors; External partners; Project teams; Health Authority Inspections; Suppliers; CMO operational meetings; QA to QA meetings", "domainKnowledge" : "Neuroscience; Biopharmaceutical; Drug discovery; Clinical development; Commercialization; Potassium channel modulator; Human genetics; Ion channel biology; Novel chemistries; Nav1.7; Kv7; Pain targets; Small molecule products; GxP", "domainList" : [ "neuroscience", "biopharmaceutical", "drug-discovery", "clinical-development", "commercialization", "potassium-channel-modulator", "human-genetics", "ion-channel-biology", "novel-chemistries", "nav1-7", "kv7", "pain-targets", "small-molecule-products", "gxp" ], "domainSpecificKnowledge" : [ "Neuroscience", "Biopharmaceutical", "Drug discovery", "Clinical development", "Commercialization", "Potassium channel modulator", "Human genetics", "Ion channel biology", "Novel chemistries", "Nav1.7", "Kv7", "Pain targets", "Small molecule products", "GxP" ], "communicationSkills" : "Proactive communication; Solution-focused communication; Communicate issues", "documentationSkills" : "Quality agreements; Audit reports; Quality systems documents; CMC documents; Health authority documents", "continuousLearning" : "Training, Learning & Development program; Tuition Assistance program", "problemSolvingSkills" : "Troubleshoot; Resolve problems", "qualificationsBasic" : "10+ years GMP quality leadership, Life sciences degree, Small molecule manufacturing experience, Early phase drug development experience, Global GxP expectations knowledge, QP requirements knowledge, Organize and multitask ability, Establish quality system metrics, Establish process indicators, Interpersonal skills, Lead cross functional projects, Work with suppliers and CMOs, Communicate proactively, Communicate solution-focused, Keep management aware, Communicate issues with CMOs, Goal oriented, Troubleshoot and resolve problems, Continuous improvement champion, Work with minimal supervision, Set priorities to meet timelines, Motivate and influence others, Team building skills, Managing skills", "qualificationsPreferred" : "Experience with small virtual company", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Who We Are: Xenon Pharmaceuticals (NASDAQ:XENE https://www.nasdaq.com/market-activity/stocks/xene) is a neuroscience-focused biopharmaceutical company dedicated to drug discovery, clinical development, and commercialization of life-changing therapeutics for patients in need. We are looking for great people who thrive in a respectful, collaborative, inclusive, and productive culture to join the Xenon team. What We Do: We are advancing an exciting product pipeline https://xenon-pharma.com/pipeline to address indications with high unmet medical need, including epilepsy, depression and pain. Our Phase 3 azetukalner program represents the most advanced, clinically validated potassium channel modulator in late-stage clinical development for multiple indications. In March 2026, we announced positive topline data from our Phase 3 X-TOLE2 study of azetukalner in focal onset seizures (FOS), and we anticipate submitting a New Drug Application to the Food and Drug Administration in the third quarter of 2026. Our Phase 3 epilepsy program also includes a second FOS study, X-TOLE3, which would support regulatory submissions outside the U.S., and the X-ACKT study in primary generalized tonic-clonic seizures, which would support regulatory submissions for an additional epilepsy indication. We also have multiple Phase 3 azetukalner clinical trials underway in major depressive disorder (MDD) and bipolar depression (BPD), based on topline data from our Phase 2 X-NOVA clinical trial. In addition, we are proud of our strong heritage in human genetics, deep understanding of ion channel biology, and expertise in novel chemistries to enable potent, selective ion channel targeting. We continue to advance an early-stage pipeline of novel therapeutic candidates, including Phase 1 studies for XEN1701 (targeting Nav1.7) and XEN1120 (targeting Kv7), which are important pain targets. Backed by a strong balance sheet to support our growth plans, we continue to build a fully integrated, premier neuroscience company with strong discovery, clinical development, corporate, and commercial operations. We are seeking a Director, Quality Assurance, GMP focusing on clinical programs to join our team. This position will be an integral member of the Quality GMP team as well as a key member of highly collaborative R&D Operations group comprised of Program Management, CMC, Regulatory, Supply Chain and Quality functions. Leveraging an extensive background in quality and manufacturing in all clinical phases will ensure the quality program requirements are met. The successful candidate will have proven leadership ability in a fast-paced and complex environment, and will interact with all levels of internal staff, as well as external advisors and partners. This position reports to the Executive Director, Quality Assurance, GMP and will be based out of Vancouver, BC, Canada or Boston, MA, USA in our Needham office. We will consider other jurisdictions for exceptional candidates. The level of the position will be commensurate with the candidate’s education and industry experience. Relocation and immigration support will be provided, if required. This role is a hybrid position, requiring a minimum of 2 days per week in the office. RESPONSIBILITIES: · Responsible for quality-related matters related to manufacturing, testing and release at a CMO (Contract Manufacturing Organization) focusing on products in the clinical stage of development. · Lead and support activities related to external quality such as, but not limited to, batch reviews and release, analytical method validations, tech transfers, deviations, quality agreements, and supplier qualifications including auditing and monitoring. · Collaborate with internal CMC functions and aligns goals and objectives for clinical phase programs and small molecule products, ensuring cGMP compliance and realization of value-added policies and best practices. · Author and review/approve quality documents including quality agreements, dispositions, Quality systems documents, audit reports, etc.... · Attend CMO and internal CMC team meetings and provide quality feedback supporting Xenon products including collaborations on complex investigations. · Support quality system and product review meetings including providing data for quality metrics (internal and vendor metrics). Provide quality reviews of key CMC and health authority documents. Review and verify data to assure compliance with data integrity. · Represent Quality function on project teams, Health Authority Inspections, suppliers and CMO operational meetings, and QA to QA meetings. · Promote a quality mindset and quality excellence approach throughout the organization. · Recruit, lead, direct, develop, coach and evaluate direct reports, if any, in accordance with the Company’s Human Resource policies and practices. · Act in accordance with Company policies, including, for example, the Code of Business Conduct and Ethics and ensure policies are understood and followed by direct reports, if any. · Some international travel may be required. · Other duties as assigned. QUALIFICATIONS: · Bachelor’s degree in a life sciences discipline, with 10+ years of experience in GMP quality leadership positions. · Strong understanding of small molecule manufacturing including drug substance manufacture, drug product manufacture with direct experience in solid oral dosage and finished goods production and distribution. · Extensive GxP knowledge with early phase drug development experience. · Experience with a small virtual company. · Strong knowledge of global GxP expectations and QP (Qualified Person) requirements. · Ability to effectively organize, multitask, and work in a fast-paced, deadline driven work environment. · Extensive experience establishing key quality system metrics and process indicators to proactively identify and address quality systems or product issues. · Strong interpersonal skills, with experience in leading cross functional projects including a successful track record working with suppliers and CMOs. · Ability to communicate in a proactive and solution-focused manner, including keeping management aware of potential issues. Ability to communicate issues with CMOs. · Goal oriented with the ability to troubleshoot and resolve problems. · Be a champion for continuous improvement in all aspects of total quality management. · Ability to work with minimal supervision, to set priorities to meet timelines, and to motivate and influence others. · Team building and managing skills including recruiting, coaching, counseling, and disciplining. Our Total Rewards program includes base salary, target bonus, and stock options, as well as a full range of benefits including medical, dental, vision, short-& long-term disability, accidental death & dismemberment, and life insurance programs, Employee Assistance Program, travel insurance, and retirement savings programs with company matching contributions. Xenon encourages time to rest and re-charge through vacation, personal days, sick days, and an end-of-year company shutdown. Xenon highly values employee development and has an expanding Training, Learning & Development program, including a Tuition Assistance program for advanced degrees.", "summaryDescription" : "Director, Quality Assurance, GMP at Xenon Pharmaceuticals. Skills: Quality Assurance, GMP, Clinical programs. Manage quality matters for CMO manufacturing. 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Israel", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 10, "experienceLevel" : "Director", "professionalSkills" : [ "Quality oversight", "Issue escalation management", "Inspection readiness", "Quality systems management", "Audit oversight", "Vendor oversight", "Compliance monitoring", "Cross-functional partnership", "Subject matter expertise" ], "hardSkillsList" : [ "GCP", "GVP", "GLP", "ICH E6", "ICH E2", "FDA regulations", "EU CTR", "OECD GLP principles" ], "softSkillsList" : [ "Leadership", "Mentoring" ], "hardSkills" : [ { "name" : "GCP", "level" : "intermediate" }, { "name" : "GVP", "level" : "intermediate" }, { "name" : "GLP", "level" : "intermediate" }, { "name" : "ICH E6", "level" : "intermediate" }, { "name" : "ICH E2", "level" : "intermediate" }, { "name" : "FDA regulations", "level" : "intermediate" }, { "name" : "EU CTR", "level" : "intermediate" }, { "name" : "OECD GLP principles", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "GCP Quality Assurance, Regulatory Inspections, Quality Management Systems", "majorSkillsList" : [ "GCP Quality Assurance", "Regulatory Inspections", "Quality Management Systems" ], "coreResponsibilities" : "Lead GCP quality oversight for clinical trials, Serve as QA interface for CROs and external, Oversee inspection readiness activities, Lead regulatory inspections, Manage quality systems, Develop, maintain, and improve GCP SOPs, Develop, maintain, and improve quality metrics, Develop, maintain, and improve KPIs, Conduct audits of clinical sites, Conduct audits of vendors, Conduct audits of CROs, Provide QA leadership for GVP activities, Provide QA leadership for GLP activities, Contribute to Quality Management System development, Promote culture of proactive quality, Promote culture of compliance", "teamCollaboration" : "Cross-functional teams; Senior stakeholders", "domainKnowledge" : "GCP; GVP; GLP; ICH E6; ICH E2; FDA regulations; EU CTR; OECD GLP principles; Neurology clinical programs; Rare diseases clinical programs; Neurodegenerative clinical programs", "domainList" : [ "gcp", "gvp", "glp", "ich-e6", "ich-e2", "fda-regulations", "eu-ctr", "oecd-glp-principles", "neurology-clinical-programs", "rare-diseases-clinical-programs", "neurodegenerative-clinical-programs" ], "domainSpecificKnowledge" : [ "GCP", "GVP", "GLP", "ICH E6", "ICH E2", "FDA regulations", "EU CTR", "OECD GLP principles", "Neurology clinical programs", "Rare diseases clinical programs", "Neurodegenerative clinical programs" ], "communicationSkills" : "Executive reporting", "documentationSkills" : "SOPs; Quality agreements", "specialRequirements" : "Occasional international travel", "qualificationsBasic" : "Bachelor’s degree or higher in life sciences, pharmacy, or related advanced degree, 10+ years of GCP Quality Assurance experience, Minimum 3 years of leadership experience in a director or senior QA role, Expertise across GCP, GVP, and GLP frameworks, Hands-on audit and inspection experience, Deep knowledge of global regulatory requirements, Proven track record of successfully leading regulatory inspections, Experience developing or significantly enhancing Quality Management Systems", "qualificationsPreferred" : "MSc, PharmD, Experience in biotech or clinical-stage organizations, Experience in neurology, rare diseases, or neurodegenerative clinical programs is a plus", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "## Accountabilities Lead end-to-end GCP quality oversight for all sponsored clinical trials, from protocol review through study closeout and clinical study report approval. Serve as the primary QA interface for CROs and external partners, ensuring consistent quality standards and effective issue escalation management. Oversee inspection readiness activities and lead regulatory inspections (FDA, EMA, MHRA, PMDA), including responses and commitment tracking. Manage quality systems including eTMF oversight, protocol deviations, GxP non-conformances, and CAPA development and resolution. Develop, maintain, and improve GCP SOPs, quality metrics, and KPIs to support continuous improvement and executive reporting. Conduct and oversee audits of clinical sites, vendors, and CROs, ensuring compliance and robust quality agreements. Provide QA leadership and subject matter expertise for GVP and GLP activities, including vendor oversight and compliance monitoring. Contribute to the development and maturation of the Quality Management System (QMS) and promote a culture of proactive quality and compliance. Act as a strategic partner to cross-functional teams and mentor junior QA professionals. Requirements: Bachelor’s degree or higher in life sciences, pharmacy, or related field; advanced degree preferred (MSc, PharmD). 10+ years of GCP Quality Assurance experience within biotech, pharmaceutical, or CRO environments. Minimum 3 years of leadership experience in a director or senior QA role, preferably in biotech or clinical-stage organizations. Strong expertise across GCP, GVP, and GLP frameworks with hands-on audit and inspection experience. Deep knowledge of global regulatory requirements including ICH E6, ICH E2, FDA regulations, EU CTR, and OECD GLP principles. Proven track record of successfully leading regulatory inspections (FDA, EMA, MHRA or equivalent). Experience developing or significantly enhancing Quality Management Systems in a biotech or mid-sized organization. Strong communication and leadership skills with the ability to influence senior stakeholders and cross-functional teams. Highly autonomous, structured, and comfortable operating in fast-paced, resource-constrained environments. Experience in neurology, rare diseases, or neurodegenerative clinical programs is a strong plus. Benefits: Competitive executive compensation aligned with experience and seniority. Fully remote flexibility across the US East Coast, Europe, or Israel. Opportunity to work on innovative clinical programs in neurology and rare disease. High-impact leadership role influencing global clinical quality strategy. Flexible work structure with international collaboration across multiple time zones. Occasional international travel for inspections, audits, and team collaboration. Exposure to cutting-edge GxP systems, global regulatory interactions, and late-stage clinical development programs. ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Director / Senior Director, GCP Quality Assurance Lead. Skills: GCP Quality Assurance, Regulatory Inspections, Quality Management Systems. Lead GCP quality oversight for clinical trials. Serve as QA interface for CROs and external", "postedDate" : "2026-06-09T12:16:55.740", "createdAt" : "2026-06-09T12:16:55.740", "lastUpdated" : "2026-06-16T01:22:57.888", "ingestTimestamp" : "2026-06-14T21:07:52.912", "mongoId" : "6a2cb20a74d8ee00a09df1bd", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 220000, "salaryAnnualMax" : 350000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "GCP", "GVP", "GLP", "ICH E6", "ICH E2", "FDA regulations", "EU CTR", "OECD GLP principles", "Leadership", "Mentoring", "GCP Quality Assurance", "Regulatory Inspections", "Quality Management Systems", "Quality oversight", "Issue escalation management", "Inspection readiness", "Quality systems management", "Audit oversight", "Vendor oversight", "Compliance monitoring", "Cross-functional partnership", "Subject matter expertise", "Neurology clinical programs", "Rare diseases clinical programs", "Neurodegenerative clinical programs" ], "skillCount" : 25, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 960.87555, "daysOld" : 6, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2cb20a74d8ee00a09df1b4", "title" : "Director / Senior Director, GCP Quality Assurance Lead", "industry" : "Others", "location" : "Germany", "locations" : [ "Germany" ], "certifications" : [ "Quality Assurance", "Clinical Research", "Regulatory Affairs" ], "timestamp" : "2026-06-15T10:28:35.613", "fingerprint" : "a725dcd3289982fdff5aff3d3634b4180936e4b91ae066a408fe72f6d02080bc", "source" : "lever", "applyUrl" : "https://jobs.lever.co/jobgether/0db444e9-50d0-4ed6-8d8f-1f60887280ce/apply", "externalId" : "0db444e9-50d0-4ed6-8d8f-1f60887280ce", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Germany", "continent" : "eu", "workMode" : "remote" } ], "locationText" : "Germany", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor", "experienceLevel" : "Director", "professionalSkills" : [ "Expertise across GCP, GVP, and GLP quality frameworks, with hands-on experience planning, conducting, and managing audits. Deep understanding of international regulatory requirements and guidelines, including ICH standards, FDA regulations, EU Clinical Trial requirements, pharmacovigilance regulations, and GLP principles. Experience within neurology, neurodegenerative diseases, rare diseases, or advanced clinical development programs is advantageous." ], "hardSkillsList" : [ "GCP", "GVP", "GLP" ], "softSkillsList" : [ "Autonomous, Proactive, Organized" ], "hardSkills" : [ { "name" : "GCP", "level" : "intermediate" }, { "name" : "GVP", "level" : "intermediate" }, { "name" : "GLP", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Autonomous, Proactive, Organized" } ], "majorSkills" : "GCP Quality Assurance, Audits, Regulatory Inspections, Quality Management System", "majorSkillsList" : [ "GCP Quality Assurance, Audits, Regulatory Inspections, Quality Management System" ], "coreResponsibilities" : "Lead and oversee GCP quality assurance activities for global clinical development programs, ensuring compliance with regulations and internal procedures. Act as the primary quality partner for clinical operations, managing external CROs and vendors, and directing inspection readiness initiatives. Maintain oversight of eTMF quality, deviations, non-conformances, CAPA, metrics, and KPIs, while also providing quality expertise for pharmacovigilance and pre-clinical activities.", "teamCollaboration" : "Represent Quality Assurance within cross-functional teams and governance forums, promoting a culture where quality supports business and clinical objectives. Mentor and develop quality team members while providing leadership and guidance across the organization.", "toolProficiency" : [ "eTMF, eQMS" ], "communicationSkills" : "Stakeholder Management", "documentationSkills" : "SOPs; eTMF quality; protocol deviations; non-conformances; CAPA management", "continuousLearning" : "Contribute to the development and continuous improvement of the Quality Management System (QMS), including SOPs, training programs, quality events, and regulatory intelligence activities.", "problemSolvingSkills" : "Risk-based quality approaches; Centralized monitoring", "specialRequirements" : "Fully remote work environment within Germany. Flexible working schedule with international collaboration across multiple time zones. Occasional international travel for business, audits, inspections, and stakeholder meetings.", "outcomesObjectives" : "Ensure studies are conducted, documented, and reported in compliance with applicable regulations, ICH guidelines, and internal procedures. Promote a culture where quality supports business and clinical objectives. Meaningful work supporting the development of innovative treatments for serious and underserved medical conditions.", "qualificationsBasic" : "Bachelor’s degree or higher in Life Sciences, Pharmacy, or a related advanced scientific or healthcare field. Extensive experience in GCP Quality Assurance within pharmaceutical, biotechnology, or CRO environments, including leadership experience at Director level or equivalent. Proven track record supporting or leading successful regulatory inspections and managing interactions with global health authorities. Experience establishing, enhancing, or maintaining quality management systems within growing or mid-sized life sciences organizations. Excellent communication and stakeholder management skills, with the ability to translate complex regulatory requirements into practical guidance.", "qualificationsPreferred" : "Experience within neurology, neurodegenerative diseases, rare diseases, or advanced clinical development programs is advantageous. Familiarity with risk-based quality approaches, centralized monitoring methodologies, and modern clinical quality strategies is considered a plus. Relevant professional certifications in quality assurance, clinical research, or regulatory affairs are desirable.", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "## Accountabilities Lead and oversee GCP quality activities across global clinical development programs, ensuring studies are conducted, documented, and reported in compliance with applicable regulations, ICH guidelines, and internal procedures. Serve as the primary quality partner for clinical operations from study startup through study completion, supporting protocol review, execution, reporting activities, and continuous inspection readiness. Manage quality oversight of external CROs, vendors, and strategic partners, ensuring alignment on quality standards, issue escalation processes, audit outcomes, and corrective actions. Direct inspection readiness initiatives and support regulatory authority inspections, coordinating responses, observation management, and regulatory commitment follow-up. Maintain oversight of eTMF quality, protocol deviations, non-conformances, CAPA management, quality metrics, and key performance indicators. Lead or support audits of clinical sites, vendors, and service providers while reviewing audit findings and ensuring effective remediation activities. Provide quality expertise and oversight for pharmacovigilance and pre-clinical activities, ensuring compliance with relevant GVP and GLP regulations and industry standards. Contribute to the development and continuous improvement of the Quality Management System (QMS), including SOPs, training programs, quality events, and regulatory intelligence activities. Represent Quality Assurance within cross-functional teams and governance forums, promoting a culture where quality supports business and clinical objectives. Mentor and develop quality team members while providing leadership and guidance across the organization. Requirements Bachelor’s degree or higher in Life Sciences, Pharmacy, or a related field; advanced scientific or healthcare qualifications are preferred. Extensive experience in GCP Quality Assurance within pharmaceutical, biotechnology, or CRO environments, including leadership experience at Director level or equivalent. Strong expertise across GCP, GVP, and GLP quality frameworks, with hands-on experience planning, conducting, and managing audits. Deep understanding of international regulatory requirements and guidelines, including ICH standards, FDA regulations, EU Clinical Trial requirements, pharmacovigilance regulations, and GLP principles. Proven track record supporting or leading successful regulatory inspections and managing interactions with global health authorities. Experience establishing, enhancing, or maintaining quality management systems within growing or mid-sized life sciences organizations. Proficiency with electronic quality systems, eTMF platforms, and quality documentation processes. Excellent communication and stakeholder management skills, with the ability to translate complex regulatory requirements into practical guidance. Highly autonomous, proactive, organized, and capable of operating effectively in a dynamic, resource-conscious environment. Experience within neurology, neurodegenerative diseases, rare diseases, or advanced clinical development programs is advantageous. Familiarity with risk-based quality approaches, centralized monitoring methodologies, and modern clinical quality strategies is considered a plus. Relevant professional certifications in quality assurance, clinical research, or regulatory affairs are desirable. Benefits Competitive senior-level compensation package. Fully remote work environment within Germany. Flexible working schedule with international collaboration across multiple time zones. Opportunity to play a key role in late-stage global clinical development programs. Exposure to cross-functional leadership and strategic decision-making. International and collaborative work environment. Professional development and leadership growth opportunities. Occasional international travel for business, audits, inspections, and stakeholder meetings. Meaningful work supporting the development of innovative treatments for serious and underserved medical conditions. ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Director / Senior Director, GCP Quality Assurance Lead. Skills: GCP Quality Assurance, Audits, Regulatory Inspections, Quality Management System. Lead and oversee GCP quality assurance activities for global clinical development programs, ensuring compliance with regulations and internal procedures. Act as the primary quality partner for clinical operations, managing external CROs and vendors, and directing inspection readiness initiatives. Maintain oversight of eTMF quality, deviations, non-conf", "postedDate" : "2026-06-10T04:05:28.356", "createdAt" : "2026-06-10T04:05:28.356", "lastUpdated" : "2026-06-15T10:28:35.613", "ingestTimestamp" : "2026-06-14T21:43:38.560", "mongoId" : "6a2cb20a74d8ee00a09df1b4", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "hasSalary" : false, "allSkills" : [ "GCP", "GVP", "GLP", "Autonomous, Proactive, Organized", "GCP Quality Assurance, Audits, Regulatory Inspections, Quality Management System", "Expertise across GCP, GVP, and GLP quality frameworks, with hands-on experience planning, conducting, and managing audits. Deep understanding of international regulatory requirements and guidelines, including ICH standards, FDA regulations, EU Clinical Trial requirements, pharmacovigilance regulations, and GLP principles. Experience within neurology, neurodegenerative diseases, rare diseases, or advanced clinical development programs is advantageous.", "Quality Assurance", "Clinical Research", "Regulatory Affairs", "eTMF, eQMS" ], "skillCount" : 10, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Director", "dataQualityScore" : 0.7777778, "_score" : 954.0699, "daysOld" : 5, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2cb20a74d8ee00a09df1ba", "title" : "Director / Senior Director, GCP Quality Assurance Lead", "industry" : "Others", "salary" : { "min" : 140000.0, "max" : 210000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Director in Biotech in Germany, adjusted for seniority and industry." }, "location" : "UK", "locations" : [ "UK" ], "timestamp" : "2026-06-16T04:27:32.481", "fingerprint" : "4438476d68346192c356e66010fe00bdde0e5cfbc5b9b111c6a4bc341a29ea07", "source" : "lever", "language" : "en", "applyUrl" : "https://jobs.lever.co/jobgether/2d7c384f-8ce2-4984-8df3-11391143a36c/apply", "externalId" : "2d7c384f-8ce2-4984-8df3-11391143a36c", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Germany", "continent" : "eu", "workMode" : "onsite" } ], "locationText" : "Germany", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceLevel" : "Director", "technicalSkills" : "GCP, GVP, GLP, ETMF", "professionalSkills" : [ "Quality assurance", "Clinical development", "Regulatory compliance", "Audit management", "Vendor management", "Inspection readiness", "Quality management", "Stakeholder management", "Team leadership", "Mentoring" ], "hardSkillsList" : [ "Protocol review", "Audit planning", "Audit conducting", "Audit management", "CAPA management", "Quality metrics", "Key performance indicators" ], "softSkillsList" : [ "Autonomous", "Organized" ], "hardSkills" : [ { "name" : "Protocol review", "level" : "intermediate" }, { "name" : "Audit planning", "level" : "intermediate" }, { "name" : "Audit conducting", "level" : "intermediate" }, { "name" : "Audit management", "level" : "intermediate" }, { "name" : "CAPA management", "level" : "intermediate" }, { "name" : "Quality metrics", "level" : "intermediate" }, { "name" : "Key performance indicators", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Autonomous" }, { "name" : "Organized" } ], "majorSkills" : "GCP Quality Assurance, Regulatory compliance, Audit management, Quality Management System", "majorSkillsList" : [ "GCP Quality Assurance", "Regulatory compliance", "Audit management", "Quality Management System" ], "coreResponsibilities" : "Lead and oversee GCP quality activities, Ensure studies are compliant with regulations, Serve as primary quality partner for clinical operations, Support protocol review, Support execution activities, Support reporting activities, Support continuous inspection readiness, Manage quality oversight of external CROs, Manage quality oversight of vendors, Manage quality oversight of strategic partners, Ensure alignment on quality standards, Ensure alignment on issue escalation processes, Ensure alignment on audit outcomes, Ensure alignment on corrective actions, Direct inspection readiness initiatives, Support regulatory authority inspections, Coordinate responses to inspections, Manage inspection observations, Follow-up on regulatory commitments, Maintain oversight of eTMF quality, Maintain oversight of protocol deviations, Maintain oversight of non-conformances, Maintain oversight of CAPA management, Maintain oversight of quality metrics, Maintain oversight of key performance indicators, Lead audits of clinical sites, Lead audits of vendors, Lead audits of service providers, Support audits of clinical sites, Support audits of vendors, Support audits of service providers, Review audit findings, Ensure effective remediation activities, Provide quality expertise for pharmacovigilance, Provide quality oversight for pharmacovigilance, Provide quality expertise for pre-clinical activities, Provide quality oversight for pre-clinical activities, Contribute to Quality Management System development, Contribute to Quality Management System improvement, Develop SOPs, Develop training programs, Manage quality events, Conduct regulatory intelligence activities, Represent Quality Assurance within cross-functional teams, Represent Quality Assurance within governance forums, Promote a culture where quality supports business objectives, Promote a culture where quality supports clinical objectives, Mentor quality team members, Develop quality team members, Provide leadership across the organization, Provide guidance across the organization", "teamCollaboration" : "Cross-functional teams; Governance forums", "projectManagementSkills" : [ "Clinical development programs" ], "domainKnowledge" : "ICH guidelines; FDA regulations; EU Clinical Trial requirements; Pharmacovigilance regulations; GLP principles; Neurology; Neurodegenerative diseases; Rare diseases", "domainList" : [ "ich-guidelines", "fda-regulations", "eu-clinical-trial-requirements", "pharmacovigilance-regulations", "glp-principles", "neurology", "neurodegenerative-diseases", "rare-diseases" ], "domainSpecificKnowledge" : [ "ICH guidelines", "FDA regulations", "EU Clinical Trial requirements", "Pharmacovigilance regulations", "GLP principles", "Neurology", "Neurodegenerative diseases", "Rare diseases" ], "toolProficiency" : [ "Electronic quality systems", "ETMF platforms" ], "communicationSkills" : "Translate regulatory requirements", "documentationSkills" : "ICH guidelines; GCP documentation", "continuousLearning" : "Professional development; Leadership growth", "specialRequirements" : "Occasional international travel", "qualificationsBasic" : "Bachelor's degree or higher, Extensive experience in GCP Quality Assurance, Leadership experience at Director level or equivalent, Expertise across GCP, GVP, and GLP quality frameworks, Hands-on experience planning, conducting, and managing audits, Deep understanding of international regulatory requirements, Proven track record supporting or leading successful regulatory inspections, Experience managing interactions with global health authorities, Experience establishing, enhancing, or maintaining quality management systems, Proficiency with electronic quality systems, Proficiency with eTMF platforms, Proficiency with quality documentation processes, Excellent communication skills, Excellent stakeholder management skills", "qualificationsPreferred" : "Life Sciences, Pharmacy, or related advanced scientific or healthcare qualifications, Experience within neurology, neurodegenerative diseases, rare diseases, Experience within advanced clinical development programs, Familiarity with risk-based quality approaches, Familiarity with centralized monitoring methodologies, Familiarity with modern clinical quality strategies, Relevant professional certifications in quality assurance, Relevant professional certifications in clinical research, Relevant professional certifications in regulatory affairs", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "## Accountabilities Lead and oversee GCP quality activities across global clinical development programs, ensuring studies are conducted, documented, and reported in compliance with applicable regulations, ICH guidelines, and internal procedures. Serve as the primary quality partner for clinical operations from study startup through study completion, supporting protocol review, execution, reporting activities, and continuous inspection readiness. Manage quality oversight of external CROs, vendors, and strategic partners, ensuring alignment on quality standards, issue escalation processes, audit outcomes, and corrective actions. Direct inspection readiness initiatives and support regulatory authority inspections, coordinating responses, observation management, and regulatory commitment follow-up. Maintain oversight of eTMF quality, protocol deviations, non-conformances, CAPA management, quality metrics, and key performance indicators. Lead or support audits of clinical sites, vendors, and service providers while reviewing audit findings and ensuring effective remediation activities. Provide quality expertise and oversight for pharmacovigilance and pre-clinical activities, ensuring compliance with relevant GVP and GLP regulations and industry standards. Contribute to the development and continuous improvement of the Quality Management System (QMS), including SOPs, training programs, quality events, and regulatory intelligence activities. Represent Quality Assurance within cross-functional teams and governance forums, promoting a culture where quality supports business and clinical objectives. Mentor and develop quality team members while providing leadership and guidance across the organization. Requirements Bachelor’s degree or higher in Life Sciences, Pharmacy, or a related field; advanced scientific or healthcare qualifications are preferred. Extensive experience in GCP Quality Assurance within pharmaceutical, biotechnology, or CRO environments, including leadership experience at Director level or equivalent. Strong expertise across GCP, GVP, and GLP quality frameworks, with hands-on experience planning, conducting, and managing audits. Deep understanding of international regulatory requirements and guidelines, including ICH standards, FDA regulations, EU Clinical Trial requirements, pharmacovigilance regulations, and GLP principles. Proven track record supporting or leading successful regulatory inspections and managing interactions with global health authorities. Experience establishing, enhancing, or maintaining quality management systems within growing or mid-sized life sciences organizations. Proficiency with electronic quality systems, eTMF platforms, and quality documentation processes. Excellent communication and stakeholder management skills, with the ability to translate complex regulatory requirements into practical guidance. Highly autonomous, proactive, organized, and capable of operating effectively in a dynamic, resource-conscious environment. Experience within neurology, neurodegenerative diseases, rare diseases, or advanced clinical development programs is advantageous. Familiarity with risk-based quality approaches, centralized monitoring methodologies, and modern clinical quality strategies is considered a plus. Relevant professional certifications in quality assurance, clinical research, or regulatory affairs are desirable. Benefits Competitive senior-level compensation package. Fully remote work environment within Germany. Flexible working schedule with international collaboration across multiple time zones. Opportunity to play a key role in late-stage global clinical development programs. Exposure to cross-functional leadership and strategic decision-making. International and collaborative work environment. Professional development and leadership growth opportunities. Occasional international travel for business, audits, inspections, and stakeholder meetings. Meaningful work supporting the development of innovative treatments for serious and underserved medical conditions. ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Director / Senior Director, GCP Quality Assurance Lead. Skills: GCP Quality Assurance, Regulatory compliance, Audit management, Quality Management System. Lead and oversee GCP quality activities. Ensure studies are compliant with regulations", "postedDate" : "2026-06-10T04:30:08.837", "createdAt" : "2026-06-10T04:30:08.837", "lastUpdated" : "2026-06-16T04:27:32.481", "ingestTimestamp" : "2026-06-14T21:06:32.203", "mongoId" : "6a2cb20a74d8ee00a09df1ba", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "Protocol review", "Audit planning", "Audit conducting", "Audit management", "CAPA management", "Quality metrics", "Key performance indicators", "Autonomous", "Organized", "GCP Quality Assurance", "Regulatory compliance", "Quality Management System", "Quality assurance", "Clinical development", "Vendor management", "Inspection readiness", "Quality management", "Stakeholder management", "Team leadership", "Mentoring", "Clinical development programs", "ICH guidelines", "FDA regulations", "EU Clinical Trial requirements", "Pharmacovigilance regulations", "GLP principles", "Neurology", "Neurodegenerative diseases", "Rare diseases", "Electronic quality systems", "ETMF platforms" ], "skillCount" : 31, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 939.7029, "daysOld" : 5, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.98 }, { "id" : "6a3050d7f292fd229cef60d1", "title" : "Director of Quality", "industry" : "Qualdoc Staffing", "salary" : { "min" : 100000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Columbus, OH", "locations" : [ "Columbus, OH" ], "certifications" : [ "Lean Manufacturing", "Six Sigma", "ASQ", "Quality certifications" ], "timestamp" : "2026-06-16T11:13:46.737", "fingerprint" : "eb013d88e927c0bc214173d2c7097c32d33c06eec4433d4ce2bc8bef80ac3322", "source" : "lever", "language" : "en", "applyUrl" : "https://jobs.lever.co/qualdoc/d93b1ba3-cb00-4f32-b5d8-36850c72c9c6/apply", "externalId" : "d93b1ba3-cb00-4f32-b5d8-36850c72c9c6", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Columbus", "state" : "Ohio", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "39.9622601,-83.0007065" } ], "locationText" : "Columbus, Ohio, United States", "experienceLevel" : "Director", "professionalSkills" : [ "Quality strategy", "Process management", "Vendor management", "Stakeholder management", "Resource planning", "Continuous improvement", "Quality systems", "Compliance programs", "Root cause analysis", "Process improvement", "Quality management", "Cross-functional leadership", "Organizational change", "Team leadership", "Supplier quality programs", "Performance metrics", "Cost of quality", "Executive reporting" ], "hardSkillsList" : [ "Quality standards", "Process controls", "Quality metrics", "Reporting systems", "Audit processes" ], "softSkillsList" : [ "Leadership", "Mentoring" ], "hardSkills" : [ { "name" : "Quality standards", "level" : "intermediate" }, { "name" : "Process controls", "level" : "intermediate" }, { "name" : "Quality metrics", "level" : "intermediate" }, { "name" : "Reporting systems", "level" : "intermediate" }, { "name" : "Audit processes", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "Quality strategy, Quality systems, Continuous improvement, Team leadership", "majorSkillsList" : [ "Quality strategy", "Quality systems", "Continuous improvement", "Team leadership" ], "coreResponsibilities" : "Develop and execute quality vision, strategy, and objectives, Establish quality goals aligned with business objectives, Promote a culture of quality, accountability, and continuous, Partner with executive leadership, engineering, operations, and supply, Lead implementation and continuous improvement of Quality Management, Ensure compliance with ISO 9001 standards and regulatory, Oversee internal and external audits, Manage corrective actions, Oversee document control, Manage quality documentation processes, Develop and standardize quality procedures, Establish quality standards throughout production, Implement process controls throughout production, Drive reductions in defects, Drive reductions in rework, Drive reductions in scrap, Drive reductions in customer complaints, Lead root cause analysis, Implement quality metrics and reporting systems, Monitor performance and identify improvement opportunities, Serve as escalation point for customer quality concerns, Support customer audits and quality reviews, Develop supplier quality programs, Develop supplier performance metrics, Collaborate with suppliers to improve quality, Collaborate with internal teams to improve quality, Lead, mentor, and develop quality personnel, Build and scale quality organization, Develop training programs for quality awareness, Develop training programs for process discipline, Foster collaboration across quality, manufacturing, engineering, and supply, Develop and maintain quality KPIs, Develop executive-level dashboards, Communicate quality performance, trends, risks, and initiatives, Monitor cost-of-quality metrics", "teamCollaboration" : "Partner with executive leadership; Partner with engineering; Partner with operations; Partner with supply chain; Collaborate with suppliers; Collaborate with internal teams; Foster collaboration across teams", "domainKnowledge" : "Manufacturing operations; ISO 9001 standards; Regulatory requirements; Quality Management System (QMS); Electrical equipment manufacturing; Industrial equipment manufacturing; Power distribution manufacturing; Control panel manufacturing; Fabrication processes; Welding processes; Machining processes; Assembly processes; Custom manufacturing processes; Engineer-to-order (ETO); Configure-to-order manufacturing", "domainList" : [ "manufacturing-operations", "iso-9001-standards", "regulatory-requirements", "quality-management-system-qms", "electrical-equipment-manufacturing", "industrial-equipment-manufacturing", "power-distribution-manufacturing", "control-panel-manufacturing", "fabrication-processes", "welding-processes", "machining-processes", "assembly-processes", "custom-manufacturing-processes", "engineer-to-order-eto", "configure-to-order-manufacturing" ], "domainSpecificKnowledge" : [ "Manufacturing operations", "ISO 9001 standards", "Regulatory requirements", "Quality Management System (QMS)", "Electrical equipment manufacturing", "Industrial equipment manufacturing", "Power distribution manufacturing", "Control panel manufacturing", "Fabrication processes", "Welding processes", "Machining processes", "Assembly processes", "Custom manufacturing processes", "Engineer-to-order (ETO)", "Configure-to-order manufacturing" ], "communicationSkills" : "Executive presentations; Reporting", "documentationSkills" : "Quality documentation", "problemSolvingSkills" : "Root cause analysis; Problem-solving", "specialRequirements" : "30% manufacturing floor engagement", "outcomesObjectives" : "Reduced defects, scrap, rework, and customer quality issues; Improved audit results and corrective action performance; Quality systems and organizational compliance; Increased customer satisfaction; Increased operational performance; Development of high-performing quality organization; Support business growth", "qualificationsBasic" : "Bachelor's degree in Engineering, Quality Management, Manufacturing, Industrial Technology, or a related field, 10+ years of quality leadership experience within a manufacturing environment, Experience leading quality systems, compliance programs, and continuous improvement initiatives, Knowledge of root cause analysis, corrective actions, process improvement methodologies, and quality management principles, Proven ability to lead cross-functional teams and drive organizational change, Excellent leadership, communication, and problem-solving skills", "qualificationsPreferred" : "Experience in electrical equipment, industrial equipment, power distribution, control panels, or similar manufacturing industries, Knowledge of fabrication, welding, machining, assembly, or custom manufacturing processes, Experience supporting engineer-to-order (ETO) or configure-to-order manufacturing environments, Understanding of ISO 9001 standards and audit processes, Lean Manufacturing, Six Sigma, ASQ, or related quality certifications", "remoteFriendly" : false, "workSiteFlexibility" : "Hybrid", "rawDescription" : "## Description Director of Quality Location: Columbus, OH Job Type: Direct Hire Salary: Starting at $100,000+ (Based on Experience) Position Overview We are seeking an experienced Director of Quality to lead quality strategy, systems, and performance across a growing manufacturing operation. This leadership role is responsible for driving quality excellence, continuous improvement, compliance, and operational performance while ensuring products and processes consistently meet customer expectations and industry standards. The ideal candidate is a strategic yet hands-on quality leader with a strong background in manufacturing environments and proven success implementing quality systems, reducing defects, and building high-performing teams. Work Environment: Approximately 70% office-based and 30% manufacturing floor engagement. ## Key Responsibilities Quality Leadership & Strategy Develop and execute the organization's quality vision, strategy, and long-term objectives. Establish quality goals aligned with business objectives and customer expectations. Promote a culture of quality, accountability, and continuous improvement. Partner with executive leadership, engineering, operations, and supply chain teams to drive quality initiatives. Quality Systems & Compliance Lead the implementation and continuous improvement of the Quality Management System (QMS). Ensure compliance with ISO 9001 standards and applicable regulatory requirements. Oversee internal and external audits, corrective actions, document control, and quality documentation processes. Develop and standardize quality procedures across manufacturing operations. Manufacturing Quality Establish quality standards and process controls throughout production operations. Drive reductions in defects, rework, scrap, and customer complaints. Lead root cause analysis and corrective action initiatives. Implement quality metrics and reporting systems to monitor performance and identify improvement opportunities. Customer & Supplier Quality Serve as the primary escalation point for customer quality concerns. Support customer audits and quality reviews. Develop supplier quality programs and performance metrics. Collaborate with suppliers and internal teams to improve product and process quality. Team Leadership & Development Lead, mentor, and develop quality personnel. Build and scale the quality organization to support business growth. Develop training programs that promote quality awareness and process discipline. Foster collaboration across quality, manufacturing, engineering, and supply chain teams. Performance Reporting Develop and maintain quality KPIs and executive-level dashboards. Communicate quality performance, trends, risks, and improvement initiatives to leadership. Monitor cost-of-quality metrics, including scrap, rework, warranty claims, and customer complaints. ## Qualifications Required Bachelor's degree in Engineering, Quality Management, Manufacturing, Industrial Technology, or a related field. 10+ years of quality leadership experience within a manufacturing environment. Experience leading quality systems, compliance programs, and continuous improvement initiatives. Strong knowledge of root cause analysis, corrective actions, process improvement methodologies, and quality management principles. Proven ability to lead cross-functional teams and drive organizational change. Excellent leadership, communication, and problem-solving skills. Preferred Experience in electrical equipment, industrial equipment, power distribution, control panels, or similar manufacturing industries. Knowledge of fabrication, welding, machining, assembly, or custom manufacturing processes. Experience supporting engineer-to-order (ETO) or configure-to-order manufacturing environments. Strong understanding of ISO 9001 standards and audit processes. Lean Manufacturing, Six Sigma, ASQ, or related quality certifications. What Success Looks Like Reduced defects, scrap, rework, and customer quality issues. Improved audit results and corrective action performance. Strong quality systems and organizational compliance. Increased customer satisfaction and operational performance. Development of a high-performing quality organization that supports business growth. ## Additional Information Why Join Us? This is an opportunity to play a key leadership role in shaping quality strategy and driving operational excellence within a growing manufacturing organization. You'll have the ability to influence company-wide initiatives, build strong teams, and make a measurable impact on product quality and customer satisfaction.", "summaryDescription" : "Director of Quality. Skills: Quality strategy, Quality systems, Continuous improvement, Team leadership. Develop and execute quality vision, strategy, and objectives. Establish quality goals aligned with business objectives", "postedDate" : "2026-06-15T18:48:08.980", "createdAt" : "2026-06-15T18:48:08.980", "lastUpdated" : "2026-06-16T11:13:46.737", "ingestTimestamp" : "2026-06-16T03:20:14.950", "mongoId" : "6a3050d7f292fd229cef60d1", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 100000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Quality standards", "Process controls", "Quality metrics", "Reporting systems", "Audit processes", "Leadership", "Mentoring", "Quality strategy", "Quality systems", "Continuous improvement", "Team leadership", "Process management", "Vendor management", "Stakeholder management", "Resource planning", "Compliance programs", "Root cause analysis", "Process improvement", "Quality management", "Cross-functional leadership", "Organizational change", "Supplier quality programs", "Performance metrics", "Cost of quality", "Executive reporting", "Manufacturing operations", "ISO 9001 standards", "Regulatory requirements", "Quality Management System (QMS)", "Electrical equipment manufacturing", "Industrial equipment manufacturing", "Power distribution manufacturing", "Control panel manufacturing", "Fabrication processes", "Welding processes", "Machining processes", "Assembly processes", "Custom manufacturing processes", "Engineer-to-order (ETO)", "Configure-to-order manufacturing", "Lean Manufacturing", "Six Sigma", "ASQ", "Quality certifications" ], "skillCount" : 44, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Director", "dataQualityScore" : 0.7777778, "_score" : 923.1948, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Manufacturing", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2ac53174d8ee00a0700b7c", "title" : "Associate Director / Director, Clinical Quality Assurance", "company" : "Beam Therapeutics", "industry" : "Biotechnology", "salary" : { "min" : 185000.0, "max" : 260000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Cambridge, Massachusetts, United States", "locations" : [ "Cambridge", "Massachusetts", "United States" ], "timestamp" : "2026-06-14T23:03:42.409", "fingerprint" : "1fb386aed534ce6243019ee1b989ba4ecc948fe64a77de65a3e0bc1f2cb692af", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/beamtherapeutics/jobs/8583858002", "externalId" : "8583858002", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Cambridge", "state" : "Massachusetts", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "42.3656347,-71.1040018" } ], "locationText" : "Cambridge, Massachusetts, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 10, "experienceLevel" : "Director", "professionalSkills" : [ "Clinical QA", "Inspection readiness", "Vendor oversight", "Program quality oversight" ], "hardSkillsList" : [ "GCP R3", "PV regulations" ], "softSkillsList" : [ "Leadership", "Judgement", "Decision making" ], "hardSkills" : [ { "name" : "GCP R3", "level" : "intermediate" }, { "name" : "PV regulations", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Judgement" }, { "name" : "Decision making" } ], "majorSkills" : "Clinical Quality Assurance, Inspection readiness, GCP compliance", "majorSkillsList" : [ "Clinical Quality Assurance", "Inspection readiness", "GCP compliance" ], "coreResponsibilities" : "Lead inspection readiness strategies, Conduct inspection risk assessments, Coordinate mock inspections, Support health authority inspections, Serve as Clinical QA Lead, Provide quality review of protocols, Provide quality review of informed consent forms, Provide quality review of investigator brochures, Provide quality review of CSRs, Provide quality review of regulatory submission documents, Develop program/study-level risk-based audit plan, Execute program/study-level risk-based audit plan, Provide quality oversight of CRO, Provide quality oversight of key service providers, Lead quality investigations, Lead root cause analysis, Lead CAPA development, Partner with Clinical Development, Partner with Clinical Operations, Partner with Data Management, Partner with Biostatistics, Partner with Medical Writing, Partner with Regulatory Affairs, Coach cross-functional teams on GCP R3, Contribute to Quality Management System evolution, Support clinical SOP development, Support QA SOP development", "teamCollaboration" : "Cross-functional teams; Clinical Development; Clinical Operations; Data Management; Biostatistics; Medical Writing; Regulatory Affairs", "domainKnowledge" : "GCP R3; PV regulations; Clinical stage biotech", "domainList" : [ "gcp-r3", "pv-regulations", "clinical-stage-biotech" ], "domainSpecificKnowledge" : [ "GCP R3", "PV regulations", "Clinical stage biotech" ], "toolProficiency" : [ "Veeva" ], "communicationSkills" : "Exceptional communication", "documentationSkills" : "Quality review", "problemSolvingSkills" : "Root cause analysis; Risk-based decision making", "qualificationsBasic" : "University degree in scientific discipline/life sciences OR equivalent experience, 10+ years of relevant experience in clinical/GCP quality, GCP R3 and solid understanding of PV regulations, Demonstrated ability to partner cross-functionally, Direct experience supporting FDA and global healthy authority inspections", "qualificationsPreferred" : "Experience in a clinical stage biotech company preferred", "remoteFriendly" : true, "rawDescription" : "Company Overview: Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases. Position Overview: Beam is seeking an experienced Clinical Quality professional at the Associate Director / Director level to join our grown Quality Team. Reporting to the Senior Director, Clinical Quality Assurance, this role will provide strategic and operational leadership for inspection readiness, program quality oversight, and vendor oversight as Beam advances toward its first regulatory submission and potential associated inspections. Responsibilities: Lead development and execution of enterprise-wide GCP inspection readiness strategies and plans. Conduct inspection risk assessments and coordinate mock inspections, readiness reviews, and remediation activities. Support health authority inspections, including document review, response coordination, and follow-up remediation activities. Serve as the Clinical QA Lead for assigned studies and programs. Provide quality review of protocols, informed consent forms, investigator brochures, CSRs, and regulatory submission documents. Develop and execute program/study-level risk-based audit plan, including investigator site, vendor and internal process audits. Provide quality oversight of CRO and key service providers through qualification, ongoing monitoring, and issue escalation. Provide QA oversight of TMF quality and completeness in collaboration with study teams and TMF group. Support TMF migration activities, as required. Lead quality investigations, root cause analysis, and CAPA development. Partner with Clinical Development, Clinical Operations, Data Management, Biostatistics, Medical Writing, and Regulatory Affairs to provide compliance and inspection readiness support. Coach cross-functional teams on GCP R3 expectations. Contribute to the continued evolution of the Quality Management System, including oversight and trending of key quality metrics (internal and external). Support clinical and QA SOP development efforts. Qualifications: University degree in a scientific discipline/life sciences OR equivalent experience in biotech/pharmaceutical industry. Experience in a clinical stage biotech company preferred. 10+ years of relevant experience in clinical/GCP quality. Level will be commensurate with experience. Outstanding expertise in GCP R3 and solid understanding of PV regulations. Demonstrated ability to successfully partner cross-functionally. Excellent interpersonal effectiveness, including exceptional communication skills. Advanced computer skills, including experience working in Veeva. Consistent excellent judgement and pragmatic, risk-based decision making skills. Direct experience supporting FDA and other global healthy authority (e.g., EMA, MHRA) inspections and related inspection preparation activities. The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data. Beam Pay Range $185,000—$260,000 USD", "summaryDescription" : "Associate Director / Director, Clinical Quality Assurance at Beam Therapeutics. Skills: Clinical Quality Assurance, Inspection readiness, GCP compliance. Lead inspection readiness strategies. Conduct inspection risk assessments", "postedDate" : "2026-06-12T02:36:40.349", "createdAt" : "2026-06-12T02:36:40.349", "lastUpdated" : "2026-06-14T23:03:42.409", "ingestTimestamp" : "2026-06-12T02:36:40.349", "mongoId" : "6a2ac53174d8ee00a0700b7c", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 185000, "salaryAnnualMax" : 260000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "GCP R3", "PV regulations", "Leadership", "Judgement", "Decision making", "Clinical Quality Assurance", "Inspection readiness", "GCP compliance", "Clinical QA", "Vendor oversight", "Program quality oversight", "Clinical stage biotech", "Veeva" ], "skillCount" : 13, "jobCategory" : "other", "jobSubcategory" : "quality", "dataQualityScore" : 1.0, "_score" : 904.20966, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotechnology" }, { "id" : "6a0dac2958b93c861ea6df14", "title" : "Psychiatrist & Medical Director, Inpatient Behavioral Health", "company" : "Mindoula Health", "industry" : "Healthcare", "salary" : { "min" : 275000.0, "max" : 425000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Director-level Psychiatrist & Medical Director in the US Healthcare industry, adjusted for seniority and location." }, "location" : "Clinton, MD", "locations" : [ "Clinton", "MD" ], "certifications" : [ "Board-certified psychiatrist" ], "timestamp" : "2026-06-15T22:19:05.789", "fingerprint" : "a662a3417a8c2b54fb7adce0976376c9f952fbf8dd9989dbe7793e6636b13f15", "source" : "breezyhr", "language" : "en", "applyUrl" : "https://mindoula-health-inc.breezy.hr/p/6fd4a3a23ac3-psychiatrist-medical-director-inpatient-behavioral-health", "externalId" : "6fd4a3a23ac3", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Clinton", "state" : "Maryland", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "38.7522607,-76.8969155" } ], "locationText" : "Clinton, Maryland, United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "majorSkills" : "Inpatient Behavioral Health, Medical Director", "majorSkillsList" : [ "Inpatient Behavioral Health", "Medical Director" ], "coreResponsibilities" : "Serve as Medical Director", "domainKnowledge" : "Behavioral Health", "domainList" : [ "behavioral-health" ], "domainSpecificKnowledge" : [ "Behavioral Health" ], "qualificationsBasic" : "Board-certified psychiatrist", "workSiteFlexibility" : "Onsite", "rawDescription" : "Psychiatrist & Medical Director, Inpatient Behavioral Health CareMind Health, the clinical services affiliate of Mindoula Health, is seeking a board-certified psychiatrist to serve as Medical Director of the Inpatient Behavioral Health Unit at Southern Maryland Hospital Center in Clinton, Mary", "summaryDescription" : "Psychiatrist & Medical Director, Inpatient Behavioral Health at Mindoula Health. 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Serve as Medical Director", "createdAt" : "2026-06-14T19:26:12.618", "lastUpdated" : "2026-06-15T22:19:05.789", "ingestTimestamp" : "2026-06-14T19:26:12.618", "mongoId" : "6a0dac2958b93c861ea6df14", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 275000, "salaryAnnualMax" : 425000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Inpatient Behavioral Health", "Medical Director", "Behavioral Health", "Board-certified psychiatrist" ], "skillCount" : 4, "jobCategory" : "healthcare", "jobSubcategory" : "support", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 901.4477, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "69c909419bc74574cbb07e10", "title" : "Psychiatrist & Medical Director, Inpatient Behavioral Health", "company" : "Mindoula Health", "industry" : "Healthcare", "salary" : { "min" : 275000.0, "max" : 425000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Director of Inpatient Behavioral Health in Leonardtown, United States, adjusted for industry and seniority." }, "location" : "Leonardtown, MD", "locations" : [ "Leonardtown", "MD" ], "certifications" : [ "Board-certified psychiatrist" ], "timestamp" : "2026-06-16T02:16:29.055", "fingerprint" : "8eef4d79015ef76f54b2de104767675bdccc055f5a3621484c8746c412667128", "source" : "breezyhr", "language" : "en", "applyUrl" : "https://mindoula-health-inc.breezy.hr/p/904b7a193c20-psychiatrist-medical-director-inpatient-behavioral-health", "externalId" : "904b7a193c20", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Leonardtown", "state" : "Maryland", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "38.2912431,-76.6357946" } ], "locationText" : "Leonardtown, Maryland, United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "majorSkills" : "Inpatient Behavioral Health, Medical Director", "majorSkillsList" : [ "Inpatient Behavioral Health", "Medical Director" ], "coreResponsibilities" : "Serve as Medical Director", "domainKnowledge" : "Behavioral Health", "domainList" : [ "behavioral-health" ], "domainSpecificKnowledge" : [ "Behavioral Health" ], "qualificationsBasic" : "Board-certified psychiatrist", "workSiteFlexibility" : "Onsite", "rawDescription" : "Psychiatrist & Medical Director, Inpatient Behavioral Health CareMind Health, the clinical services affiliate of Mindoula Health, is seeking a board-certified psychiatrist to serve as Medical Director of the Inpatient Behavioral Health Unit at St. Mary’s Hospital in Leonardtown, Maryland. This", "summaryDescription" : "Psychiatrist & Medical Director, Inpatient Behavioral Health at Mindoula Health. Skills: Inpatient Behavioral Health, Medical Director. Serve as Medical Director", "createdAt" : "2026-06-14T18:40:07.143", "lastUpdated" : "2026-06-16T02:16:29.055", "ingestTimestamp" : "2026-06-14T18:40:07.143", "mongoId" : "69c909419bc74574cbb07e10", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 275000, "salaryAnnualMax" : 425000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Inpatient Behavioral Health", "Medical Director", "Behavioral Health", "Board-certified psychiatrist" ], "skillCount" : 4, "jobCategory" : "healthcare", "jobSubcategory" : "support", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 897.3465, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a305b87f292fd229cf5ebc4", "title" : "Senior Quality Assurance Engineer", "industry" : "Technology", "salary" : { "min" : 135000.0, "max" : 195000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Quality Assurance Engineer in Los Angeles, adjusted for the technology industry and senior experience level." }, "location" : "Los Angeles, CA", "locations" : [ "Los Angeles, CA" ], "timestamp" : "2026-06-16T07:01:03.519", "fingerprint" : "af269ac9eb3b196e32f4228f3d50ab9013f9c40e3f16c169e583164773f2daa8", "source" : "jazzhr", "language" : "en", "externalId" : "TDjevYH2eQ", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Los Angeles", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "34.0536909,-118.2427660" } ], "locationText" : "Los Angeles, California, United States", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Python, Java, JavaScript, SQL, API, CI/CD, Cloud platforms, Containerization technologies", "professionalSkills" : [ "Test automation", "API testing", "Performance testing", "Security testing", "CI/CD pipelines" ], "hardSkillsList" : [ "Test automation", "API testing", "Performance testing", "Security testing", "CI/CD pipelines" ], "hardSkills" : [ { "name" : "Test automation", "level" : "intermediate" }, { "name" : "API testing", "level" : "intermediate" }, { "name" : "Performance testing", "level" : "intermediate" }, { "name" : "Security testing", "level" : "intermediate" }, { "name" : "CI/CD pipelines", "level" : "intermediate" } ], "majorSkills" : "Quality Assurance, Test Automation, API Testing", "majorSkillsList" : [ "Quality Assurance", "Test Automation", "API Testing" ], "coreResponsibilities" : "Develop and execute test plans, Design and implement automated tests, Perform manual testing, Identify and document defects, Collaborate with development teams, Participate in code reviews, Contribute to CI/CD pipeline improvements, Stay updated on QA best practices", "teamCollaboration" : "Development teams; Cross-functional teams", "projectManagementSkills" : [ "Agile", "Scrum" ], "domainKnowledge" : "Software development lifecycle", "domainList" : [ "software-development-lifecycle" ], "domainSpecificKnowledge" : [ "Software development lifecycle" ], "toolProficiency" : [ "Selenium", "Cypress", "Postman", "JIRA", "Git" ], "communicationSkills" : "Technical documentation", "documentationSkills" : "Test plans; Test cases; Defect reports", "continuousLearning" : "Professional development", "problemSolvingSkills" : "Root cause analysis; Troubleshooting", "outcomesObjectives" : "Ensure high-quality software releases; Improve test coverage; Reduce production defects", "qualificationsBasic" : "5+ years of experience in QA, Experience with test automation frameworks, Experience with API testing, Experience with performance testing, Experience with security testing, Experience with CI/CD pipelines", "qualificationsPreferred" : "Experience with cloud platforms, Experience with containerization technologies, Experience with database testing, Experience with mobile testing, Experience with accessibility testing, Experience with performance testing tools, Experience with security testing tools", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "summaryDescription" : "Senior Quality Assurance Engineer. Skills: Quality Assurance, Test Automation, API Testing. Develop and execute test plans. Design and implement automated tests", "createdAt" : "2026-06-15T22:23:01.854", "lastUpdated" : "2026-06-16T07:01:03.519", "ingestTimestamp" : "2026-06-15T22:23:01.854", "mongoId" : "6a305b87f292fd229cf5ebc4", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 135000, "salaryAnnualMax" : 195000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Test automation", "API testing", "Performance testing", "Security testing", "CI/CD pipelines", "Quality Assurance", "Test Automation", "API Testing", "Agile", "Scrum", "Software development lifecycle", "Selenium", "Cypress", "Postman", "JIRA", "Git" ], "skillCount" : 16, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 0.5555556, "_score" : 893.6891, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c8b7c74d8ee00a0972f0f", "title" : "CX Quality Assurance Lead", "company" : "Headway", "industry" : "All Cost Centers", "salary" : { "min" : 95200.0, "max" : 140000.0, "currency" : "USD", "frequency" : "Yearly" }, "location" : "Remote", "locations" : [ "Remote" ], "timestamp" : "2026-06-15T22:43:19.535", "fingerprint" : "61c4fbc331ea503d03408c18950843527e93cef709df7e21ed0f5b54422edf57", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/headway/30ee5b07-cb45-4a59-9944-d8df07b4e217/application", "externalId" : "30ee5b07-cb45-4a59-9944-d8df07b4e217", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Bulgaria", "continent" : "eu", "workMode" : "remote" } ], "locationText" : "Bulgaria", "employmentType" : "FULL_TIME", "experienceMinYears" : 8, "experienceMaxYears" : 15, "experienceLevel" : "Lead", "technicalSkills" : "SQL", "professionalSkills" : [ "Program ownership", "Data analysis" ], "hardSkillsList" : [ "Quality assurance", "Conversation analytics", "AI-powered quality measurement" ], "hardSkills" : [ { "name" : "Quality assurance", "level" : "intermediate" }, { "name" : "Conversation analytics", "level" : "intermediate" }, { "name" : "AI-powered quality measurement", "level" : "intermediate" } ], "majorSkills" : "Quality assurance, Conversation analytics, AI-powered quality measurement", "majorSkillsList" : [ "Quality assurance", "Conversation analytics", "AI-powered quality measurement" ], "coreResponsibilities" : "Own QA program area end-to-end, Drive QA program from signal to action, Set quality standards and rubric logic, Ensure consistent application across channels, Recommend framework updates based on outcomes, Configure and improve AI-QA tooling, Set scoring logic, Monitor accuracy, Ensure platform delivers consistent output, Build automation into QA workflows, Expand AI-assisted processes, Analyze quality and conversation data, Surface DSAT drivers, Surface behavioral trends, Surface escalation patterns, Surface workflow gaps, Understand why issues occur, Design and maintain dashboards, Track key quality metrics, Translate findings into recommendations, Produce structured insight reports, Ensure findings flow into decisions, Contribute QA input to WBR/MBR cycles, Partner with BPO teams, Align on standards with BPO teams, Drive calibration with BPO teams, Keep expectations consistent, Collaborate with Enablement, Collaborate with Knowledge, Collaborate with Programs, Ensure quality signals drive decisions, Deliver initiatives to improve agent quality, Deliver initiatives to improve customer satisfaction", "teamCollaboration" : "CX leadership; BPO teams; Enablement teams; Knowledge teams; Programs teams", "domainKnowledge" : "Mental healthcare; Insurance billing; Provider software", "domainList" : [ "mental-healthcare", "insurance-billing", "provider-software" ], "domainSpecificKnowledge" : [ "Mental healthcare", "Insurance billing", "Provider software" ], "toolProficiency" : [ "ObserveAI", "Rippit", "Level AI", "Klaus", "Looker", "Metabase", "Hex" ], "continuousLearning" : "Training and professional development", "problemSolvingSkills" : "Root cause analysis", "outcomesObjectives" : "Improve agent quality; Improve customer satisfaction", "qualificationsBasic" : "4–7 years in CX operations, QA, or analytics, Owned a program with measurable outcomes", "qualificationsPreferred" : "Looker, Metabase, Hex, or SQL experience, Experience with ObserveAI, Rippit, Level AI, Klaus, or similar", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "1 in 4 people in the US have a treatable mental health condition, but most providers don't accept insurance, making therapy too expensive for most people. Headway’s mission is to fix this by building a new mental healthcare system everyone can access. We started by solving the biggest barrier to care: insurance. The admin work - credentialing, claims, payment reconciliation - is a nightmare. We've automated that. But we're going further. Over 75,000 providers across all 50 states run their practice on our software, serving over 1 million patients. We are building the best tools for therapists to run their entire practice, reimagining the experience of finding a therapist, and investing in the platform foundations to enable this at scale. We aren't just a billing layer; we are becoming the platform where care actually happens. We're a Series D company with $325M+ in funding (a16z, Accel, Spark Capital, etc.), looking for exceptional people to help us achieve this mission. We want your time here to be the most meaningful experience of your career. Join us, and help change mental healthcare for the better. About the Role Headway is looking for an experienced QA Lead to evolve how quality works across our CX organization as we move from manual evaluation to a system that generates insights continuously, surfaces behavioral trends at scale, and drives the decisions that make our agents better and our customers better served. This is a customer support quality assurance role focused on agent evaluation, conversation analytics, and AI-powered quality measurement — not software testing, test automation, or CI/CD engineering You'll be joining the Agent Success team within Customer Experience, a function focused on making our CX agents more effective, more consistent, and better supported. QA is in active evolution here; we're moving from a manual, sampling-based model to a specialized, insight-driven system, and the people we hire will have a direct hand in building it. Your role will have real ownership over a defined area of the QA program — calibration and framework governance, AI-powered analytics and insights, or vendor and partner quality oversight, depending on role fit. This isn't a traditional QA role where you spend your days manually grading interactions. You'll design the systems, analyze the signals, and surface the patterns that change how we operate, with clear ownership over outcomes. Your work will give CX leadership consistent, reliable visibility into performance, process, and operations — and the context to act on what they find. You will: - Own a defined area of the QA program end-to-end (calibration and rubric governance, AI-powered analytics, or partner quality) and drive it from signal to action - Set quality standards and rubric logic for your area; ensure consistent application across channels and partners and recommend framework updates based on outcomes - Configure and continuously improve AI-QA tooling (ObserveAI or similar) with set scoring logic, monitoring accuracy, and ensuring the platform delivers consistent, actionable output - Build automation into QA workflows to reduce manual overhead and expand coverage; establish AI-assisted processes for status updates, reporting, and initiative recaps - Analyze quality and conversation data to surface DSAT drivers, behavioral trends, escalation patterns, and workflow gaps by going beyond what happened to understand why - Design and maintain dashboards that track key quality metrics; translate findings into clear operational recommendations for CX leadership - Produce structured insight reports (clear signal, root cause, recommended action) and ensure findings flow into training, content, coaching, and product decisions - Contribute QA input to WBR/MBR cycles and cross-functional planning; give leadership consistent visibility into program health and customer experience impact - Partner with BPO teams and CX stakeholders to align on standards, drive calibration, and keep expectations consistent across every channel and partner - Collaborate with Enablement, Knowledge, and Programs to ensure quality signals drive decisions across training, content, and coaching and deliver initiatives that measurably improve agent quality and customer satisfaction You'd be a great fit if... - 4–7 years in CX operations, QA, or analytics — you've genuinely owned a program (not just contributed to one) and have specific, measurable outcomes to point to - Comfortable pulling and analyzing data without a dedicated analyst (Looker, Metabase, Hex, or similar; SQL is a plus) - You've worked with QA and conversation intelligence tools (ObserveAI, Rippit, Level AI, Klaus, or similar) and know how to configure, calibrate, and get meaningful output from them - You use AI as part of how you actually work with automations, workflow improvements, faster paths to insight - You've produced insight reports that moved real decisions, where training shifted, processes changed, policy updated - You don't just identify problems, you design the processes that prevent them from recurring - You can translate quality data for non-QA audiences and influence decisions without formal authority - You are comfortable in ambiguity and move fast without sacrificing rigor, and you're fine building the playbook as you go - You are fluent in quality evaluation methodologies, calibration processes, and QA framework design - You have a track record coordinating across operations, training, content, and technology teams to deliver shared goals - You are a strong communicator, demonstrated with clear status reports, insight briefs, and stakeholder presentations - You are motivated by the mission: making mental healthcare affordable and accessible Compensation and Benefits: The expected base pay range for this position is $95,200-$140,000, based on a variety of factors including qualifications, experience, and geographic location. In addition to base salary, this role may be eligible for an equity grant, depending on the position and level. We are committed to offering a comprehensive and competitive total rewards package, including robust health and wellness benefits, retirement savings, and meaningful ownership opportunities through equity. Compensation decisions are made holistically, ensuring fairness and alignment with market benchmarks while recognizing individual contributions and potential. - Benefits offered include: - Equity compensation - Medical, Dental, and Vision coverage - HSA / FSA - 401K - Work-from-Home Stipend - Therapy Reimbursement - 16-week parental leave for eligible employees - Carrot Fertility annual reimbursement and membership - 13 paid holidays each year as well as a Holiday Break during the week between December 25th and December 31st - Flexible PTO - Employee Assistance Program (EAP) - Training and professional development We believe a team's strength is in its people, and we cannot achieve this mission without a team that reflects the diversity of this problem – across race, ethnicity, gender, sexuality, age, national origin, religion, family status, disability, military status, and experience. Headway is committed to the full inclusion of all qualified individuals. As part of this commitment, Headway will ensure that persons with disabilities are provided with reasonable accommodations. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or receive other benefits and privileges of employment, please inform the recruiter when they contact you to schedule your interview. Headway participates in E-Verify. To learn more, click here. https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf A notice to Headway applicants: To protect yourself against phishing and recruitment fraud, please note that Headway only accepts applications through our official careers page at https://headway.co/careers. Headway will never refer you to external websites, ask for payment or personal information, or conduct interviews via messaging apps. All official communication will come from a @findheadway.com http://findheadway.com email address. If you are contacted by someone claiming to be from Headway via an unofficial channel, please do not share any information and report it as spam.", "summaryDescription" : "CX Quality Assurance Lead at Headway. Skills: Quality assurance, Conversation analytics, AI-powered quality measurement. Own QA program area end-to-end. Drive QA program from signal to action", "createdAt" : "2026-06-14T20:13:41.920", "lastUpdated" : "2026-06-15T22:43:19.535", "ingestTimestamp" : "2026-06-14T20:13:41.920", "mongoId" : "6a2c8b7c74d8ee00a0972f0f", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 95200, "salaryAnnualMax" : 140000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Quality assurance", "Conversation analytics", "AI-powered quality measurement", "Program ownership", "Data analysis", "Mental healthcare", "Insurance billing", "Provider software", "ObserveAI", "Rippit", "Level AI", "Klaus", "Looker", "Metabase", "Hex" ], "skillCount" : 15, "jobCategory" : "sales", "jobSubcategory" : "customer_success", "seniorityLevel" : "Lead", "dataQualityScore" : 0.8888889, "_score" : 870.421, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.97 }, { "id" : "6a307f24f292fd229c05598b", "title" : "Quality Assurance Technician", "company" : "Sunrise Farms", "industry" : "QA", "salary" : { "min" : 53000.0, "max" : 56000.0, "currency" : "CAD", "frequency" : "yearly" }, "location" : "Cloverdale, BC", "locations" : [ "Cloverdale, BC" ], "timestamp" : "2026-06-16T13:54:34.386", "fingerprint" : "5b05069ac5f125d184b0230030a3a438ae05fd40592cefcd4ede8ee619308a45", "source" : "lever", "language" : "en", "applyUrl" : "https://jobs.lever.co/sunrisefarms/c041eefe-3688-44ce-99a0-f0af86ee0c4e/apply", "externalId" : "c041eefe-3688-44ce-99a0-f0af86ee0c4e", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Cloverdale", "state" : "British Columbia", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "49.1161848,-122.7214847" } ], "locationText" : "Cloverdale, British Columbia, Canada", "employmentType" : "CONTRACT", "minimumEducation" : "Bachelor's", "experienceMinYears" : 1, "technicalSkills" : "Food Science, Chemical", "professionalSkills" : [ "Time management", "Analytical skill" ], "hardSkillsList" : [ "Quality control", "Data entry", "Reporting", "Process control", "Food safety", "HACCP Principles", "Sanitation", "GMP compliance", "Sensory evaluation", "Microbial testing" ], "hardSkills" : [ { "name" : "Quality control", "level" : "intermediate" }, { "name" : "Data entry", "level" : "intermediate" }, { "name" : "Reporting", "level" : "intermediate" }, { "name" : "Process control", "level" : "intermediate" }, { "name" : "Food safety", "level" : "intermediate" }, { "name" : "HACCP Principles", "level" : "intermediate" }, { "name" : "Sanitation", "level" : "intermediate" }, { "name" : "GMP compliance", "level" : "intermediate" }, { "name" : "Sensory evaluation", "level" : "intermediate" }, { "name" : "Microbial testing", "level" : "intermediate" } ], "majorSkills" : "Quality Assurance, HACCP, Food Safety", "majorSkillsList" : [ "Quality Assurance", "HACCP", "Food Safety" ], "coreResponsibilities" : "Evaluate HACCP programs, Assess Quality Assurance Programs, Maintain compliance with guidelines, Perform auditing, Perform inspection, Perform product quality control, Enter data, Report findings, Report collected data, Verify compliance, Identify need for corrective action, Support Operations, Meet food safety requirements, Follow food safety procedures, Follow quality procedures, Perform pre-operational inspection, Perform line checks, Monitor line settings, Document line settings, Adhere to food safety, Adhere to HACCP Principles, Audit compliance level, Assess compliance level, Report compliance level, Perform critical control point checks, Perform pre shipment reviews, Perform allergen checks, Perform other QA duties, Troubleshoot processing lines, Provide solutions to operations, Evaluate held product, Suggest disposition, Inform Quality Assurance personnel, Inspect raw material products, Inspect outgoing product, Report deficiencies, Report off-specification product, Perform various inspections, Complete QC-related documents, Review production records, Verify production records, Monitor GMP compliance, Collect samples, Perform sensory evaluation, Perform in-house laboratory testing", "teamCollaboration" : "Support to Operations", "domainKnowledge" : "CFIA SFCR; GFSI; HACCP; Food safety; GMP", "domainList" : [ "cfia-sfcr", "gfsi", "haccp", "food-safety", "gmp" ], "domainSpecificKnowledge" : [ "CFIA SFCR", "GFSI", "HACCP", "Food safety", "GMP" ], "toolProficiency" : [ "Microsoft Office" ], "communicationSkills" : "Verbal; Writing", "documentationSkills" : "Reporting findings; Documenting data; Process control documentation; QC-related documents; Production records", "problemSolvingSkills" : "Analytical skill; Troubleshoot processing lines; Provide solutions", "specialRequirements" : "Work shifts, Work overtime, Flexible to work shifts", "qualificationsBasic" : "University/Diploma Food Science, 1 year related experience, Basic CFIA SFCR knowledge, Basic GFSI knowledge, Microsoft Office proficiency", "qualificationsPreferred" : "Meat industry experience preferred", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "## Description Sunrise Farms is a group of companies with primary focus in the poultry industry. From our hatcheries to our “ready to eat” state of the art cooking facilities we service customers in the retail, food service and industrial sectors. We are proud of our support of the Canadian farm as well as our investment in the latest equipment and technologies at our facilities across Canada. Our test kitchens have the most current cooking equipment replicating that used in commercial establishments, to facilitate precision testing. This way you know the product you receive will perform to your expectations. We are proud of our long-standing partnerships with family-owned Canadian chicken farmers to produce high quality products. Role: Quality Control Technician is responsible for evaluating and assessing that HACCP and Quality Assurance Programs are properly maintained in compliance with regulatory guidelines though auditing/inspection, product quality control, data entry and reporting findings and data collected to verify compliance or to identify a need for corrective action. In addition the Quality Control Technician will provide support to Operations with the objective of meeting food safety requirements efficiently. The Quality Control Technician will be responsible for following established food safety and quality procedures. ## Responsibilities Perform pre-operational inspection on operating equipment when required before handing off for start-up. Perform all line checks to ensure compliance with product specifications. Monitor all line settings and document in accordance with process control requirements. Adhere to food safety and HACCP Principles. Audit, assess and report compliance level for documented process control standards Perform critical control point checks, pre shipment reviews, allergen checks on process as outlined in the HACCP requirements and other QA duties defined within the Quality Assurance Plan Trouble shoot processing lines and provide solutions to operations that target manufacturing and food safety requirements Evaluate held product, suggest disposition and inform appropriate Quality Assurance personnel as required Inspect raw material products and outgoing product and report any deficiencies and off-specification product to Quality Assurance Manager Perform various inspections (ie. daily operational inspection, room temperature monitoring, metal detection verification, building inspection, locker inspection) Complete QC-related documents with accuracy and error-free Review and verify production records for completion and accuracy Ongoing GMP compliance monitoring Responsible for sample (swabs, raw materials, products) collection Responsible for sensory evaluation and in-house laboratory organoleptic and microbial product testing ## Requirements University/Bachelor/Diploma of Food Science & chemical or Equivalent Minimum one year of related experience, preferably in the meat industry Basic knowledge of CFIA SFCR, GFSI (BRC) requirements Attention to detail with good time management skill Good communication skill (verbal and writing) Good analytical skill and be able to take appropriate immediate actions to ensure food safety is not compromised Proficiency in Microsoft Office Flexible to work shifts and overtime ## Additional Information #INDLP #LI-SJ At Sunrise Farms we are proud to be an equal-opportunity employer. All qualified individuals, regardless of race, color, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or any other identifying characteristic are encouraged to apply. Please note that the expected new hire salary range provided is derived from a group of like roles within Sunrise Farms. The final offer amount for this role will be dependent on geographical region, applicable experience, and skillset of the candidate.", "summaryDescription" : "Quality Assurance Technician at Sunrise Farms. Skills: Quality Assurance, HACCP, Food Safety. Evaluate HACCP programs. Assess Quality Assurance Programs", "postedDate" : "2026-06-15T20:54:47.014", "createdAt" : "2026-06-15T20:54:47.014", "lastUpdated" : "2026-06-16T13:54:34.386", "ingestTimestamp" : "2026-06-16T03:24:25.514", "mongoId" : "6a307f24f292fd229c05598b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "50k-75k", "hasSalary" : false, "allSkills" : [ "Quality control", "Data entry", "Reporting", "Process control", "Food safety", "HACCP Principles", "Sanitation", "GMP compliance", "Sensory evaluation", "Microbial testing", "Quality Assurance", "HACCP", "Food Safety", "Time management", "Analytical skill", "CFIA SFCR", "GFSI", "GMP", "Microsoft Office" ], "skillCount" : 19, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Junior", "dataQualityScore" : 0.8888889, "_score" : 869.7329, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Food & Beverage", "llmIndustryConfidence" : 0.95 }, { "id" : "69dde3e52beec4dd3d9a03fa", "title" : "Data Analysis and Quality Assurance Director", "company" : "Texas Workforce Commission", "industry" : "Government", "salary" : { "min" : 155000.0, "max" : 220000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Director of Data Analysis and Quality Assurance in Austin, Texas, adjusted for government industry and seniority." }, "location" : "826770", "locations" : [ "826770", "
Austin:1117 Trinity St (320TX-4002)
1117 Trinity St
Austin, 78701-1919

" ], "timestamp" : "2026-06-15T08:50:23.902", "fingerprint" : "59540f617c815fc9a9369d5c690638b92eadeb9abb68f7061cbad208bee2e008", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa270.taleo.net/careersection/ex/jobdetail.ftl?job=34107", "externalId" : "34107", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Austin", "state" : "Texas", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "30.2711286,-97.7436995" } ], "locationText" : "Austin, Texas, United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "technicalSkills" : "SQL, Python, R, Scala, Spark, Dbt, Tableau, Power BI, Looker, Snowflake, BigQuery, Redshift, Databricks, Fivetran, Airflow, Delta Lake, Scikit-learn, TensorFlow, PyTorch, XGBoost, LightGBM, Hugging Face, MLflow, AWS, GCP, Azure", "professionalSkills" : [ "Strategic planning", "Policy development", "Data analysis", "Reporting", "Quality assurance", "Process improvement", "Forecasting", "Modeling" ], "hardSkillsList" : [ "Data reporting", "Data analysis", "Statistical methods", "ML frameworks", "BI platforms", "Cloud data stacks", "Modelling skills", "Regression", "Classification", "Clustering", "Time-series analysis", "A/B testing", "Causal inference" ], "hardSkills" : [ { "name" : "Data reporting", "level" : "intermediate" }, { "name" : "Data analysis", "level" : "intermediate" }, { "name" : "Statistical methods", "level" : "intermediate" }, { "name" : "ML frameworks", "level" : "intermediate" }, { "name" : "BI platforms", "level" : "intermediate" }, { "name" : "Cloud data stacks", "level" : "intermediate" }, { "name" : "Modelling skills", "level" : "intermediate" }, { "name" : "Regression", "level" : "intermediate" }, { "name" : "Classification", "level" : "intermediate" }, { "name" : "Clustering", "level" : "intermediate" }, { "name" : "Time-series analysis", "level" : "intermediate" }, { "name" : "A/B testing", "level" : "intermediate" }, { "name" : "Causal inference", "level" : "intermediate" } ], "majorSkills" : "Data analysis, Quality assurance, Data engineering, Machine learning", "majorSkillsList" : [ "Data analysis", "Quality assurance", "Data engineering", "Machine learning" ], "coreResponsibilities" : "Direct data reporting and analysis activities, Develop techniques for analyzing and reporting data, Remain compliant with state and federal rules, Develop and establish goals and objectives, Provide direction, guidance, and assistance in developing reports, Provide direction, guidance, and assistance in collecting data, Review and approve reports, Review and approve data collection, Review and approve analysis, Ensure accuracy of reports, Ensure quality reports are distributed, Review guidelines, procedures, rules, Monitor compliance related to contract and procurement databases, Make recommendations to improve data collection, Make recommendations to improve data analysis, Plan, develop, and approve schedules, Plan, develop, and approve priorities, Plan, develop, and approve standards, Review results of special investigations, Review results of internal audits, Review results of research studies, Review results of forecasts, Review results of modeling exercises, Provide direction and guidance, Perform advanced managerial work, Provide direction and guidance in strategic operations, Provide direction and guidance in planning, Establish goals and objectives, Respond to audit requests, Develop guidelines, procedures, policies, rules, and regulations, Develop schedules, priorities, and standards, Coordinate data collection, Coordinate reporting, Coordinate quality, Evaluate data collection, Evaluate reporting, Evaluate quality, Develop data reports, Develop policies and procedures for producing quality reports, Develop policies and procedures for maintaining data integrity, Plan work of others, Assign work of others, Supervise work of others", "teamCollaboration" : "Cross-functional teams; Internal audits; External audits", "projectManagementSkills" : [ "Strategic planning", "Policy development", "Roadmap planning" ], "domainKnowledge" : "Procurement; Contract management; State data reporting; Federal regulations", "domainList" : [ "procurement", "contract-management", "state-data-reporting", "federal-regulations" ], "domainSpecificKnowledge" : [ "Procurement", "Contract management", "State data reporting", "Federal regulations" ], "toolProficiency" : [ "Dbt Cloud" ], "communicationSkills" : "Executive presentations; Technical documentation; Client meetings", "documentationSkills" : "Technical writing; API documentation; Architecture diagrams", "continuousLearning" : "Training and development opportunities", "innovationCreativity" : "Innovative ideas; Streamline processes", "problemSolvingSkills" : "Problem solver; Root cause analysis; Data-driven decision making", "specialRequirements" : "Texas resident required, Relocate to Texas required", "outcomesObjectives" : "Ensure departmental processes are impartial; Ensure departmental processes are transparent; Ensure departmental processes are professional; Acquisitions of program services for the State", "qualificationsBasic" : "Five years of experience in oversight and direction of an agency or in strategic planning and policy development and implementation, Two years of experience in administrative management or supervisory capacity, Two years of experience in data collection and analysis, One year experience in management and direction of staff relevant to data collection and analysis, Experience with state data reporting and analysis", "qualificationsPreferred" : "PhD preferred, Specific ML framework experience, Cloud platform certs", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Data Analysis and Quality Assurance (DAQA) Director Who We Are: Texas Workforce Commission connects people with careers across the state. We are based in Austin on the east side of the Texas State Capitol, in the Business Operations Division located at 1117 Trinity Street in Austin. We're a Family Friendly Certified Workplace with great work-life balance, competitive salaries, extensive opportunities for training and development, and fantastic benefits. TWC is not considering applications from individuals who require sponsorship for an employment visa, including those with H1B visas or those currently on student or postgraduate visas. You must be a Texas resident to work for the Texas Workforce Commission or willing to relocate to Texas. Who You Are: A self-starting, motivated, collaborative problem solver who understands the value of data analysis in measurement of procurement and contract related activities for the Procurement and Contract Services Department. You should share our department’s mission to provide excellent customer service and ensure that departmental processes are impartial, transparent, and professional. You should be innovative and open to new ideas to streamline existing processes. We strive to ensure that acquisitions of program services are conducted with the best outcome for the State in mind. What you Will Do: The Data Analysis and Quality Assurance (DAQA) Director: -Directs data reporting and analysis activities. -Develops and implements techniques for analyzing and reporting data in meaningful ways and remains compliant with state and federal rules and regulations. -Develops and establishes goals and objectives consistent with the agency policy and procedure. -Provides direction, guidance, and assistance in developing reports and collecting data related to contracts and procurement. -Reviews and approves reports, data collection and analysis, and ensures accuracy and that quality reports are distributed. -Reviews guidelines, procedures, rules, and regulations; and monitors compliance related to contract and procurement databases. -Makes recommendations to improve data collection and analysis. -Plans, develops, and approves schedules, priorities, and standards for achieving goals. -Reviews results of special investigations, internal audits, research studies, forecasts, and modeling exercises to provide direction and guidance. -Performs advanced (senior-level) managerial work providing direction and guidance in strategic operations and planning. Works under minimal supervision, with extensive latitude for the use of initiative and independent judgment. You Will be Trusted To: -Establish goals and objectives. -Respond to audit requests from internal and external entities. -Develop guidelines, procedures, policies, rules, and regulations. -Develop schedules, priorities, and standards for achieving established goals. -Coordinate and evaluate data collection, reporting, and quality. -Develop and evaluate data reports and policies and procedures for producing quality reports and maintaining data integrity. -Plan, assign, and supervise the work of others. -Work under limited supervision, with considerable latitude for the use of initiative and independent judgment. -Performs other duties as assigned. You Qualify With: -Five years of full-time experience in the oversight and direction of an agency program; or in strategic planning and policy development and implementation, two years of which must have been in an administrative management or supervisory capacity. -Relevant academic credits may be applied toward experience qualifications for this position. You Are a Great Fit With: -A minimum of two years’ experience in data collection and analysis. -One year experience in the management and direction of staff relevant to data collection and analysis. -Experience with state data reporting and analysis. You Gain: -A Family Friendly Certified Workplace. -Competitive starting salary: $9,166.67 to $9,583.34/month, depending on experience -Defined Retirement Benefit Plan -Optional 401(k) and 457 accounts -Medical Insurance -Paid time off, including time for vacation, sick and family care leave -Additional benefits for active employees can be found at https://www.ers.texas.gov/Active-Employees/Health-Benefits. VETERANS: Use your military skills to qualify for this position or other jobs! Go to www.texasskillstowork.com to translate your military work experience and training courses into civilian job terms, qualifications, and skill sets. Also, you can compare this position to military occupations (MOS) at the Texas State Auditor's Office by pasting this link into your browser: https://hr.sao.texas.gov/Compensation/MilitaryCrosswalk/MOSC_ProgramManagement.pdf HOW TO APPLY: To be considered, please complete a State of Texas Application for Employment and apply online at www.workintexas.com or on Taleo ( Job Search ). TWC is not considering applications from individuals who require sponsorship for an employment visa, including those with H1B visas or those currently on student or postgraduate visas In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire. A position utilizing this classification will be designated as security sensitive according to the Texas Labor Code, Section 301.042. United States-Texas-Austin", "summaryDescription" : "Data Analysis and Quality Assurance Director at Texas Workforce Commission. Skills: Data analysis, Quality assurance, Data engineering, Machine learning. Direct data reporting and analysis activities. Develop techniques for analyzing and reporting data", "createdAt" : "2026-06-14T01:12:18.507", "lastUpdated" : "2026-06-15T08:50:23.902", "ingestTimestamp" : "2026-06-14T01:12:18.507", "mongoId" : "69dde3e52beec4dd3d9a03fa", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 155000, "salaryAnnualMax" : 220000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Data reporting", "Data analysis", "Statistical methods", "ML frameworks", "BI platforms", "Cloud data stacks", "Modelling skills", "Regression", "Classification", "Clustering", "Time-series analysis", "A/B testing", "Causal inference", "Quality assurance", "Data engineering", "Machine learning", "Strategic planning", "Policy development", "Reporting", "Process improvement", "Forecasting", "Modeling", "Roadmap planning", "Procurement", "Contract management", "State data reporting", "Federal regulations", "Dbt Cloud" ], "skillCount" : 28, "jobCategory" : "engineering", "jobSubcategory" : "data", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 867.494, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Government", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2af78174d8ee00a073d5a7", "title" : "Director Quality Assurance", "company" : "Astrazeneca", "salary" : { "min" : 174856.0, "max" : 262285.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "United States of America", "locations" : [ "United States of America" ], "timestamp" : "2026-06-14T22:28:46.491", "fingerprint" : "1ee32496b71026c6ba91b0dab77748fe050845b15e8508ee968d8e3c403a6bc8", "source" : "workday", "language" : "en", "applyUrl" : "https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/US---Rockville---MD/Director-Quality-Assurance_R-254341", "externalId" : "R-254341", "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "hybrid" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 5, "experienceLevel" : "Director", "professionalSkills" : [ "Quality Assurance", "Cell Therapy", "Biologics Quality", "Product launches", "Regulatory frameworks", "GxP regulations" ], "hardSkillsList" : [ "Clinical lot release", "Health authority inspections", "Change management" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Clinical lot release", "level" : "intermediate" }, { "name" : "Health authority inspections", "level" : "intermediate" }, { "name" : "Change management", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "Quality Assurance, Cell Therapy, Regulatory compliance", "majorSkillsList" : [ "Quality Assurance", "Cell Therapy", "Regulatory compliance" ], "coreResponsibilities" : "Lead the new Quality Assurance team at the, Support facility start-up and routine production, Partner with senior leaders across AstraZeneca to ensure, Participate in investigations, assessments, and evaluations of quality, Manage, develop, and lead a team of Quality, Develop strategic and operational plans, Lead high-level projects, Define innovative solutions within complex areas of the", "teamCollaboration" : "Working with a global team; Partner with senior leaders", "projectManagementSkills" : [ "Lead high-level projects" ], "domainKnowledge" : "Cell Therapy; Biologics Quality Assurance; Clinical lot release; Product launches; Health authority inspections; Global commercial product distribution; Cell Therapy regulatory inspections", "domainList" : [ "cell-therapy", "biologics-quality-assurance", "clinical-lot-release", "product-launches", "health-authority-inspections", "global-commercial-product-distribution", "cell-therapy-regulatory-inspections" ], "domainSpecificKnowledge" : [ "Cell Therapy", "Biologics Quality Assurance", "Clinical lot release", "Product launches", "Health authority inspections", "Global commercial product distribution", "Cell Therapy regulatory inspections" ], "documentationSkills" : "Quality records; Deviations; CAPAs; Change controls", "innovationCreativity" : "Define innovative solutions", "problemSolvingSkills" : "Root cause analysis; Investigations; Assessments; Evaluations", "qualificationsBasic" : "B. S. degree in Science, Engineering, Pharmacy, or related technical field with a minimum of 8 years of applicable experience, M. S. degree in Science, Engineering, Pharmacy, or related technical field with a minimum of 5 years of applicable experience, Minimum of 5 years of management experience, Minimum of 2 years of Cell Therapy/Biologics Quality Assurance experience including clinical lot release, Experience with product launches, Experience with health authority inspections, Experience with global commercial product distribution requirements, Proven ability to work in a fast-paced environment across multiple technical functions, Demonstrated ability to make decisions under pressure that balance patient safety, compliance, and supply, Ability to influence senior stakeholders, both internally and externally", "qualificationsPreferred" : "Advanced degree in Science, Engineering, Biochemistry, Pharmacy, or related technical field, Minimum of 2 years of Cell Therapy Quality Assurance experience including clinical lot release, Demonstrated track record in leadership of change management in a positive and non-disruptive manner to the company’s values, Experience with Cell Therapy regulatory inspections, Experience engaging with global regulatory bodies, Proven track record of attracting and developing talent, Extensive working knowledge of international Cell Therapy GxP regulatory frameworks, regulations, and guidance", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Join us as a **Director Quality Assurance** , where you will lead and direct the Site Quality Assurance Operations at our Cell Therapy 9950 MCD Rockville manufacturing site. This role offers an opportunity to develop strategic and operational plans, lead high-level projects, and define innovative solutions within complex areas of the business. You will be working on diversified tasks with a global team, providing you with exposure to new ways of thinking and helping us grow collectively and as individuals. **What you will do:** * Lead the new Quality Assurance team at the Commercial Cell Therapy Facility, supporting facility start-up and routine production. * Partner with senior leaders across AstraZeneca to ensure delivery of an integrated approach to Cell Therapy Quality. * Participate in investigations, assessments, and evaluations of quality records such as deviations, CAPAs, and change controls. * Manage, develop, and lead a team of Quality Assurance professionals. **Minimum Qualifications:** * B.S. degree in Science, Engineering, Pharmacy, or related technical field with a minimum of 8 years of applicable experience * M.S. degree in Science, Engineering, Pharmacy, or related technical field with a minimum of 5 years of applicable experience * Minimum of 5 years of management experience * Minimum of 2 years of Cell Therapy/Biologics Quality Assurance experience including clinical lot release * Experience with product launches, health authority inspections, and global commercial product distribution requirements * Proven ability to work in a fast-paced environment across multiple technical functions. * Demonstrated ability to make decisions under pressure that balance patient safety, compliance, and supply. * Ability to influence senior stakeholders, both internally and externally **Preferred Qualifications:** * Advanced degree in Science, Engineering, Biochemistry, Pharmacy, or related technical field * Minimum of 2 years of Cell Therapy Quality Assurance experience including clinical lot release * Demonstrated track record in leadership of change management in a positive and non-disruptive manner to the company’s values. * Experience with Cell Therapy regulatory inspections * Experience engaging with global regulatory bodies. * Proven track record of attracting and developing talent. * Extensive working knowledge of international Cell Therapy GxP regulatory frameworks, regulations, and guidance The annual base salary for this position ranges from $174,856 - $262,285 USD. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program. Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn't mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, we take Quality seriously. Our work is important and valued. We are always innovating, and trialling the latest models and technologies to improve reliability and excellence in our processes. We are proactive, science-based, and solutions-oriented. It's our ambition to go far that keeps pushing us forward. But it's our pragmatic focus that keeps us delivering what will have the biggest impact on our patients. We are strong communicators and networkers. With constant exposure to different tasks, we're at our best when we're working together as a team. Ready to make a difference? Apply today! **Date Posted** 11-Jun-2026 **Closing Date** 02-Aug-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.", "summaryDescription" : "Director Quality Assurance at Astrazeneca. Skills: Quality Assurance, Cell Therapy, Regulatory compliance. Lead the new Quality Assurance team at the. Support facility start-up and routine production", "postedDate" : "2026-06-12T07:00:28.931", "createdAt" : "2026-06-12T07:00:27.743", "lastUpdated" : "2026-06-14T22:28:46.491", "ingestTimestamp" : "2026-06-12T07:00:27.743", "mongoId" : "6a2af78174d8ee00a073d5a7", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/US---Rockville---MD/Director-Quality-Assurance_R-254341", "salaryAnnualMin" : 174856, "salaryAnnualMax" : 262285, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Clinical lot release", "Health authority inspections", "Change management", "Leadership", "Quality Assurance", "Cell Therapy", "Regulatory compliance", "Biologics Quality", "Product launches", "Regulatory frameworks", "GxP regulations", "Lead high-level projects", "Biologics Quality Assurance", "Global commercial product distribution", "Cell Therapy regulatory inspections" ], "skillCount" : 15, "jobCategory" : "engineering", "seniorityLevel" : "executive", "dataQualityScore" : 1.0, "_score" : 859.14594, "daysOld" : 2, "hasLocation" : true, "hasGeo" : false }, { "id" : "6a305935f292fd229cf45cce", "title" : "Quality Director", "salary" : { "min" : 175000.0, "max" : 275000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Director of Quality in Georgetown, United States, adjusted for seniority and industry." }, "location" : "Georgetown, TX", "locations" : [ "Georgetown, TX" ], "timestamp" : "2026-06-16T06:47:41.098", "fingerprint" : "73ecdee1ff4733f456e9393fbb3e0f16a0870000d650392617e7ab28e5cdc587", "source" : "jazzhr", "language" : "en", "externalId" : "lyKhCX1jks", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Georgetown", "state" : "Texas", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "30.6370152,-97.6775634" } ], "locationText" : "Georgetown, Texas, United 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: true, "estimation_basis" : "The estimation is based on the market baseline for a Director of Quality & Project Delivery in Bulgaria, adjusted for the energy industry and director-level seniority." }, "location" : "Remote Office ", "locations" : [ "Remote Office" ], "certifications" : [ "OSHA 30 General Industry or Construction", "CQM", "CQA" ], "timestamp" : "2026-06-16T05:08:16.142", "fingerprint" : "2d01ce916c124a20c2b0456be8f0f46c3f4eb0ee0d4f40fbf1c9e8f4bb0e0173", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/actpowerservices/jobs/7770379003", "externalId" : "7770379003", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Bulgaria", "continent" : "eu", "workMode" : "remote" } ], "locationText" : "Bulgaria", "employmentType" : "FULL_TIME", "experienceMinYears" : 10, "experienceLevel" : "Director", "professionalSkills" : [ "Construction management", "Project management", "Quality assurance", "Quality control" ], "hardSkillsList" : [ "Scoping", "Estimating", "Scheduling" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Scoping", "level" : "intermediate" }, { "name" : "Estimating", "level" : "intermediate" }, { "name" : "Scheduling", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "Quality assurance, Project delivery, Process management", "majorSkillsList" : [ "Quality assurance", "Project delivery", "Process management" ], "coreResponsibilities" : "Review O&M findings, Drive closure of non-conformances, Integrate QA/QC requirements into project planning, Integrate QA/QC requirements into project execution, Set clear expectations for team members, Hold team members accountable, Foster a culture of quality, Foster a culture of continuous improvement, Foster a culture of accountability, Identify staffing needs, Build team capacity, Support planning of large solar projects, Support execution of large solar projects, Support planning of complex solar projects, Support execution of complex solar projects, Assist project managers in scoping, Assist project managers in estimating, Assist project managers in scheduling, Assist project managers in executing high-priority projects, Establish expectations with clients, Review submittals, Enforce compliance with quality requirements, Negotiate quality disputes with clients, Negotiate quality disputes with contractors, Resolve quality disputes with clients, Resolve quality disputes with contractors, Escalate unresolved issues, Keep clients informed, Keep internal leadership informed, Prepare formal quality reports, Prepare lessons learned, Prepare program updates for clients, Prepare program updates for executives", "teamCollaboration" : "Partner with operations; Partner with project management; Partner with field teams; Collaborate with operations leadership; Collaborate with AOT leadership", "projectManagementSkills" : [ "Scoping", "Estimating", "Scheduling" ], "domainKnowledge" : "BESS commissioning processes; Renewable operations", "domainList" : [ "bess-commissioning-processes", "renewable-operations" ], "domainSpecificKnowledge" : [ "BESS commissioning processes", "Renewable operations" ], "communicationSkills" : "Formal quality reports; Lessons learned; Program updates", "problemSolvingSkills" : "Root cause analysis", "specialRequirements" : "Ability to travel up to 50%, Overnight travel, Out-of-state travel, Work in various weather conditions, Comply with safety standards, PPE required, Sit for extended periods, Stoop for extended periods, Kneel for extended periods, Bend for extended periods, Stand for extended periods, Walk for extended periods, Lift up to 50 pounds, Push up to 50 pounds, Pull up to 50 pounds, Travel to project sites, Overnight stays required", "outcomesObjectives" : "Maximize production; Preserve compliance; Ensure safety of personnel; Ensure safety of communities", "qualificationsBasic" : "10+ years progressive experience in quality assurance/quality control, construction management, or project management, Valid Driver’s License, OSHA 30 General Industry or Construction certification", "qualificationsPreferred" : "Project management and quality management software experience preferred, CQM, CQA, or equivalent quality certification a plus", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "ACT Power Services was created to provide industry leading services for our clients. As an independent service provider, we avoid conflicts of interest and maintain a complete focus on our clients’ needs. We have taken a no-frills approach to developing our organization to ensure our clients are only paying for services that add value. ACT then leverages a world-class team, state of the art technology, and best-in-class operating practices to ensure every facility is operated in a manner that maximizes production, preserves compliance, and ensures the safety of our personnel and communities. Our vision is to reshape the industry’s benchmark for renewable operations and create the next generation of O review findings and drive closure of non-conformances Partner with operations, project management, and field teams to integrate QA/QC requirements into project planning and execution from day one Team Building set clear expectations and hold team members accountable to ACT’s standards Foster a culture of quality, continuous improvement, and accountability across all organizational levels Collaborate with operations and AOT leadership to identify staffing needs and build team capacity in alignment with project pipeline growth AOT Project Support Serve as a senior resource within the Asset Optimization Team (AOT) to support the planning and execution of large, complex solar projects Assist AOT project managers in scoping, estimating, scheduling, and executing high-priority O establish expectations, review submittals, and enforce compliance with ACT’s quality requirements Negotiate and resolve quality disputes with clients and contractors in a professional, solutions-oriented manner Escalate unresolved issues appropriately while keeping clients and internal leadership informed throughout the resolution process Prepare and deliver formal quality reports, lessons learned, and program updates for client and executive audiences Required Skills/Abilities: 10+ years of progressive experience in quality assurance/quality control, construction management, or O experience with project management and quality management software preferred Valid Driver’s License with a clean driving record; ability to travel up to 50% including overnight and out-of-state travel OSHA 30 General Industry or Construction certification preferred; CQM, CQA, or equivalent quality certification a plus Knowledge of Battery Energy Storage System (BESS) construction and commissioning processes, including safety protocols, integration requirements, and quality hold points Physical Requirements: Work is performed both in a reporting setting and outdoors at various project sites across all weather conditions Must be able to comply with all safety standards and procedures; PPE is required in all field environments Must have the ability to sit, stoop, kneel, bend, stand, or walk for extended periods Must be able to lift, push, or pull up to 50 pounds on an occasional basis Valid driver’s license required; travel to project sites required, including overnight stays Benefits: 401(k) with employer match Health Insurance Dental Insurance Vision Insurance Flexible Spending Account Health Savings Account Short-term and Long-term disability Critical illness Paid Time Off Parental Leave Paid Holidays Employee assistance program Life insurance Opportunities for advancement Training and Development Legal and Identity Theft Company vehicle or stipend opportunities ACT Power Services does not accept any unsolicited resumes or referrals from any third-party recruiting firms or agencies.", "summaryDescription" : "Director of Quality & Project Delivery at ACT Power Services. Skills: Quality assurance, Project delivery, Process management. Review O&M findings. 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Liaise with PSI divisions; Liaise with vendors; Communication point for Operations staff; Communication point for clients", "projectManagementSkills" : [ "Quality management" ], "domainKnowledge" : "Life science; Contract Research Organization", "domainList" : [ "life-science", "contract-research-organization" ], "domainSpecificKnowledge" : [ "Life science", "Contract Research Organization" ], "toolProficiency" : [ "MS Project" ], "communicationSkills" : "Presentation skills", "documentationSkills" : "Assemble QA study audits documentation", "qualificationsBasic" : "3 years in quality management, 2 to 3 supervised QA audits, Full working proficiency in English, Full working proficiency in Japanese", "qualificationsPreferred" : "Bachelor or above degree in life science, MS Office applications proficiency, MS Project proficiency", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "PSI is a leading Contract Research Organization with 30 years in the industry offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. SCOPE OF RESPONSIBILITIES 1. Communication 1.1. Serves as the communication point to project teams with regard to quality assurance (QA) study audits 1.2. Follows up with project teams with regard to resolution of PSI QA study audits 1.3. Liaises with PSI divisions/operational offices with regard to internal systems, process, and location audits 1.4. Liaises with vendors with regard to vendor qualification audits 1.5. Serves as the communication point for PSI Operations staff with regard to issues related to quality assurance 1.6. Serves as the communication point for PSI clients with regard to QA audits contracted to PSI 2. Planning and scheduling 2.1. Prepares, conducts, and reports QA study audits 2.2. Assembles QA study audits documentation 2.3. Takes part in the preparation, conduct, and reporting of internal systems audits 2.4. Takes part in the preparation, conduct, and reporting of internal locations audits 2.5. Takes part in the preparation, conduct, and reporting of vendor qualification audits 2.6. Takes part in the preparation, conduct, and reporting of internal process audits 3. Training 3.1. Trains PSI Operations staff in quality management topics ## Qualifications 1. Bachelor or above degree in life science or an equivalent combination of education 2. Minimum of 3 years in quality management or quality assurance, 2 to 3 supervised QA audits is a must 3. Full working proficiency in English and Japanese 4. Communication, presentation, and customer-service skills 5. Team building, leadership and organizational skills 6. Proficiency in MS Office applications, including MS Project ## Additional Information Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.", "summaryDescription" : "Quality Assurance Auditor at PSI CRO. Skills: Quality assurance, Study audits, Vendor qualification. Serve as communication point to project teams. 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We focus on delivering quality and on-time services across a variety of therapeutic indications. SCOPE OF RESPONSIBILITIES 1. Communication 1.1. Serves as the communication point to project teams with regard to quality assurance (QA) study audits 1.2. Follows up with project teams with regard to resolution of PSI QA study audits 1.3. Liaises with PSI divisions/operational offices with regard to internal systems, process, and location audits 1.4. Liaises with vendors with regard to vendor qualification audits 1.5. Serves as the communication point for PSI Operations staff with regard to issues related to quality assurance 1.6. Serves as the communication point for PSI clients with regard to QA audits contracted to PSI 2. Planning and scheduling 2.1. Prepares, conducts, and reports QA study audits 2.2. Assembles QA study audits documentation 2.3. Takes part in the preparation, conduct, and reporting of internal systems audits 2.4. Takes part in the preparation, conduct, and reporting of internal locations audits 2.5. Takes part in the preparation, conduct, and reporting of vendor qualification audits 2.6. Takes part in the preparation, conduct, and reporting of internal process audits 3. Training 3.1. Trains PSI Operations staff in quality management topics ## Qualifications 1. Bachelor or above degree in life science or an equivalent combination of education 2. Minimum of 3 years in quality management or quality assurance, 2 to 3 supervised QA audits is a must 3. Full working proficiency in English and Japanese 4. Communication, presentation, and customer-service skills 5. Team building, leadership and organizational skills 6. Proficiency in MS Office applications, including MS Project ## Additional Information Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.", "summaryDescription" : "Quality Assurance Auditor at PSI CRO. Skills: Quality assurance, Study audits, Vendor qualification. Serve as communication point to project teams. Follow up with project teams", "postedDate" : "2026-06-15T10:33:18.000", "createdAt" : "2026-06-16T00:16:43.156", "lastUpdated" : "2026-06-16T08:36:03.159", "ingestTimestamp" : "2026-06-16T00:16:43.156", "mongoId" : "6a305e6cf292fd229cf7070e", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "QA study audits", "Internal systems audits", "Internal locations audits", "Vendor qualification audits", "Internal process audits", "Presentation", "Customer-service", "Team building", "Leadership", "Organizational skills", "Quality assurance", "Study audits", "Vendor qualification", "Quality management", "Process audits", "Quality management topics", "Contract Research Organization", "MS Project" ], "skillCount" : 18, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 1.0, "_score" : 822.0531, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c79a074d8ee00a09420be", "title" : "Quality Assurance Lead", "company" : "Wedgewood Pharmacy", "salary" : { "min" : 55000.0, "max" : 65000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Albany, OH", "locations" : [ "Albany", "OH" ], "timestamp" : "2026-06-16T03:26:11.090", "fingerprint" : "d5f6085f8b32afcf90f736938fbf2c3a25fd23c6e19946c5c892690dda1cc2f1", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/wedgewoodpharmacy/jobs/4284336009", "externalId" : "4284336009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Albany", "state" : "Ohio", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "39.2275735,-82.2023695" } ], "locationText" : "Albany, Ohio, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 8, "experienceMaxYears" : 15, "experienceLevel" : "Lead", "remoteFriendly" : false, "rawDescription" : "At Wedgewood Pharmacy, we are dedicated to improving the lives of animals through customized medication and compassionate care. Every role in our organization contributes to helping pets live healthier, happier lives. We are a team driven by purpose, quality, and a shared commitment to animal health. We are seeking a Quality Assurance Lead to join our team in Albany, Ohio. This position reports to the Quality Assurance Manager. You will be primarily responsible for the environmental monitoring program, document control management, and training. Experience in Environmental Monitoring; specifically, performing or overseen: Viable Air Sampling, Non-Viable Particulate Monitoring, Surface Monitoring, Personnel Monitoring, Trend Analysis, Excursion Investigations (OOS) and Environmental Monitoring Reporting . Experience with Quality Systems, Including: Change Control, Deviations, CAPAs, Document Control, Training Systems, Risk Assessments and Internal audits. Prefer Regulatory experience: FDA 21 CFR 210, 211, 21 CFR Part 11, FDA Aseptic Processing Guidance, USP , USP , 503B Outsourcing Facility Guidance The Basics Location: Albany, Ohio Job Type: Regular Full-Time Schedule: Monday–Friday, 6:00 AM–2:30 PM Compensation: $55,000 - $65,000 How You’ll Make an Impact Actively seek to resolve any concerns while adhering to the company policy and standards of behavior QA lead is responsible for leading his/her team. This often involves resolving conflicts between individual team members or even between different teams. QA lead will also mentor his/her team and motivate them during both the stressful times and the slow times on the job. QA lead will define strategies to ensure the product being released is up to industry and company standards. QA lead creates plans, including individual phases, and ensure the team meets the deadlines set forth in those plans. In order to maintain deadlines, QA lead will also evaluate the team throughout to identify areas where improvement can be made. Will support compliance with the appropriate internal and external regulatory requirements and maintain awareness of the overall regulatory landscape. Will be responsible for compiling and reporting monthly metrics related to quality systems. Provides expertise and guidance in interpreting policies, regulatory and/or governmental regulations and facilitates uniform standards worldwide and enables best practice sharing, thereby fostering the achievement of company’s mission globally. Will liaise and communicate with Quality assurance, Quality control, Validation department in regard to any changes or improvements in QMS or regular day to day duties. Take part in internal audit as well as any risk assessment. QA lead identifies risk and creates plans to mitigate it. QA leads also hold regular team meetings to identify new risks and create new mitigation plans on the fly. Leads also encourage their team members to do the same. What We're Looking For Bachelor’s degree in Microbiology, Biology, Chemistry, Biochemistry, Pharmaceutical Sciences, Engineering, Animal Sciences, or related scientific discipline Minimum 3-5 years of experience in FDA-regulated pharmaceutical, medical device, biologics, sterile compounding, or other cGMP-regulated environments Experience in Animal Science or food industry is highly desirable Strong knowledge of quality systems (Quality Planning, Management Review, Internal Audit, CAPA, Document Controls, etc.) Experience analyzing company needs and ability to effectively organize and manage multiple company initiatives and encourage coworkers to do the same Proficient using Microsoft Suite and other data entry software Strong understanding of business goals and standards for customer service Extensive knowledge of management strategies and practical application in the workplace What You’ll Love About Wedgewood Competitive compensation and benefits Opportunities for growth and career development A supportive, team-first culture where your work matters The ability to make a real impact on animal health every day Pay Range $55,000—$65,000 USD Why We Do What We Do At Wedgewood Pharmacy, your work has purpose. Every prescription you help prepare, support, or deliver contributes to improving the health and well-being of animals. We are passionate about what we do and proud to build a workplace where people feel supported, included, and valued. Our Commitment to Inclusion Wedgewood Pharmacy is an equal opportunity employer. We are committed to building a diverse and inclusive workplace where everyone can thrive.", "summaryDescription" : "Quality Assurance Lead at Wedgewood Pharmacy", "postedDate" : "2026-06-14T21:47:33.023", "createdAt" : "2026-06-14T21:47:33.023", "lastUpdated" : "2026-06-16T03:26:11.090", "ingestTimestamp" : "2026-06-14T21:47:33.023", "mongoId" : "6a2c79a074d8ee00a09420be", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 55000, "salaryAnnualMax" : 65000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Lead", "dataQualityScore" : 0.8888889, "_score" : 810.2346, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Pharma", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c8e5474d8ee00a097ba6e", "title" : "Director / Senior Director, GCP Quality Assurance Lead (US/IL/EU)", "company" : "Prilenia Therapeutics", "industry" : 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Lead inspection readiness for regulatory authority inspections, Serve as primary QA contact for inspections, Coordinate responses to observations, Oversee regulatory commitment closure, Author and maintain GCP SOPs, Define and track quality metrics and KPIs, Oversee clinical site review reports, Oversee CRO review reports, Oversee vendor review reports, Manage CAPA review, Approve Quality Agreements, Serve as GVP QA partner, Serve as GVP SME, Oversee PV systems, Oversee vendor quality performance, Oversee vendor support CAPA resolution, Ensure compliance with EU GvP modules, Ensure compliance with FDA 21 CFR Part 312, Ensure compliance with ICH E2 series, Serve as GLP QA partner, Serve as GLP SME, Ensure compliance with OECD Principles of GLP, Ensure compliance with national regulations, Contribute to Prilenia's QMS, Contribute to SOP lifecycle, Contribute to quality event tracking, Contribute to training, Contribute to regulatory intelligence, Represent QA on clinical program teams, Represent QA on governance forums, Champion a proactive quality and compliance culture, Make quality an enabler of clinical program success, Mentor junior QA staff, Foster professional development within quality function", "teamCollaboration" : "Clinical Development; Regulatory Affairs; Drug Safety; Biostatistics; CRO QA teams; Ferrer's QA function; Clinical program teams; Governance forums", "projectManagementSkills" : [ "CAPA management" ], "domainKnowledge" : "GCP; GvP; GLP; Neurodegenerative diseases; Neurodevelopmental disorders; Huntington's Disease; ALS; Sigma-1 receptor agonist; ICH guidelines; FDA regulations; EU regulations; OECD Principles of GLP; Data integrity principles", "domainList" : [ "gcp", "gvp", "glp", "neurodegenerative-diseases", "neurodevelopmental-disorders", "huntington-s-disease", "als", "sigma-1-receptor-agonist", "ich-guidelines", "fda-regulations", "eu-regulations", "oecd-principles-of-glp", "data-integrity-principles" ], "domainSpecificKnowledge" : [ "GCP", "GvP", "GLP", "Neurodegenerative diseases", "Neurodevelopmental disorders", "Huntington's Disease", "ALS", "Sigma-1 receptor agonist", "ICH guidelines", "FDA regulations", "EU regulations", "OECD Principles of GLP", "Data integrity principles" ], "toolProficiency" : [ "Veeva Vault", "Wingspan" ], "communicationSkills" : "Translate regulatory requirements; Clear guidance", "specialRequirements" : "Occasional travel, International travel", "outcomesObjectives" : "Ensure compliance with regulations; Drive CAPA resolution; Successful inspection outcomes", "qualificationsBasic" : "Bachelor’s degree or higher in life sciences, pharmacy, or related field, Minimum 10 years of GCP QA experience, At least 3 years in leadership or director-level role, Hands-on experience conducting and managing audits in GCP, GvP, and GLP, Deep knowledge of ICH E6(R2/R3), Deep knowledge of ICH E2 series, Deep knowledge of FDA 21 CFR Parts 11/50/54/56/312, Deep knowledge of EU Clinical Trials Regulation (No. 536/2014), Deep knowledge of EU GvP modules, Deep knowledge of OECD Principles of GLP, Proven experience leading regulatory authority inspections, Experience building or maturing a QMS, Proficiency with eTMF systems, Proficiency with electronic QMS platforms, Exceptional communication skills, Highly autonomous, Proactive, Comfortable in fast-paced environment", "qualificationsPreferred" : "Master’s degree (MSc, PharmD) preferred, Experience in neurology, neurodegenerative disease, or rare disease clinical programs, Familiarity with risk-based monitoring (RBM), Familiarity with centralized monitoring, Familiarity with ICH E6(R3) risk-proportionate approaches, Professional certification: RQAP-GCP (SQA), Professional certification: RAC (RAPS), Professional certification: CCRA (ACRP), Experience supporting NDALA/MAA submissions, Experience supporting post-approval quality oversight, Knowledge of 21 CFR Part 11 / Annex 11, Knowledge of data integrity principles (ALCOA+)", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "## Description About Prilenia Prilenia Therapeutics, a clinical-stage biotechnology company focused on the urgent mission of developing novel therapeutics to slow the progression of neurodegenerative diseases and neurodevelopmental disorders, is looking for a Director/Senior Director, GCP Quality Assurance Lead, to support programs in both Huntington’s Disease and ALS. We are a flexible, fast-moving team that is quickly advancing a potential therapy poised to have major impact on the lives of patients and their families. Our lead product candidate, pridopidine, holds Orphan Drug Designation in both Huntington’s disease (HD) and amyotrophic lateral sclerosis (ALS) in the U.S. and EU, as well as Fast Track designation from the FDA for the treatment of HD. Prilenia is conducting global Phase 3 clinical trials in both HD and ALS. Pridopidine has the potential to be a pivotal treatment to address HD and ALS disease progression. Prilenia believes pridopidine’s novel mechanism of action as a Sigma-1 receptor agonist also gives it potential in numerous other neurodegenerative and neurodevelopmental conditions. To learn more about our story and company culture, visit us at https://Prilenia.com About the role The Director/Sr. Dir, GCP Quality Assurance is Prilenia's primary quality lead for clinical development, owning GCP quality end-to-end from study start-up through inspection readiness, and serving as sponsor QA counterpart to our CRO(s) and Ferrer's QA team. The role also provides proportionate QA oversight for pharmacovigilance (GVP) and pre-clinical (GLP) activities. The ideal candidate is both a hands-on quality practitioner and a strategic partner to Clinical Development, Regulatory Affairs, Drug Safety, and Biostatistics, combining deep GCP/GvP/GLP expertise with the executive presence to influence cross-functional teams and senior leadership. ## Roles and Responsibilities GCP Quality - Core Focus Ensure all Prilenia-sponsored trials are conducted, documented, and reported in compliance with applicable regulations, ICH guidelines, and Prilenia's SOPs. Serve as Prilenia's day-to-day QA lead for Phase 3 clinical operations, embedded in the program team from protocol review through clinical study report sign-off. Act as sponsor QA counterpart to CRO QA teams and to Ferrer's QA function, maintain quality oversight of outsourced trial execution, align on standards, and manage issue escalation. Oversee eTMF quality, manage protocol deviations and GxP non-conformances, drive CAPA resolution with CROs and sites, and maintain continuous inspection readiness. Lead inspection readiness and management for regulatory authority inspections (FDA, EMA, MHRA, PMDA); serve as primary QA contact, coordinate responses to observations, and oversee regulatory commitment closure. Author and maintain GCP and related SOPs; define and track quality metrics and KPIs for senior leadership. Oversee clinical site, CRO, and vendor audits; review reports, manage CAPA resolution; review and approve Quality Agreements. QA Partnership & SME for GLP and GVP Serve as GVP QA partner and SME to Drug Safety: oversee PV systems, vendor quality performance, and vendor audits; support CAPA resolution for safety findings; ensure compliance with EU GvP modules, FDA 21 CFR Part 312, and ICH E2 series. Serve as GLP QA partner and SME for externally conducted pre-clinical studies; ensure compliance with OECD Principles of GLP and applicable national regulations. QMS & Cross-Functional Leadership Contribute to Prilenia's fit-for-purpose QMS, SOP lifecycle, quality event tracking, training, and regulatory intelligence. Represent QA on clinical program teams and relevant governance forums. Champion a proactive quality and compliance culture, making quality an enabler of clinical program success rather than a compliance exercise. Mentor junior QA staff and foster professional development within the quality function. ## Qualifications Required Bachelor’s degree or higher in life sciences, pharmacy, or a related discipline; advanced degree (MSc, PharmD) preferred. Minimum 10 years of GCP QA experience within the pharmaceutical, biotechnology, or CRO industry, with at least 3 years in a leadership or director-level role at a biotech company. Demonstrated expertise across GCP, GvP, and GLP quality frameworks; hands-on experience conducting and managing audits in all three domains. Deep knowledge of ICH E6(R2/R3), ICH E2 series, FDA 21 CFR Parts 11/50/54/56/312, EU Clinical Trials Regulation (No. 536/2014), EU GvP modules, and OECD Principles of GLP. Proven experience leading or managing regulatory authority inspections (FDA, EMA, MHRA, or equivalent) to successful outcomes. Experience building or significantly maturing a QMS in a small-to-mid-size pharmaceutical setting. Proficiency with eTMF systems (e.g., Veeva Vault, Wingspan) and electronic QMS platforms. Exceptional communication skills; able to translate complex regulatory requirements into clear guidance for diverse audiences. Highly autonomous, proactive, and resilient; comfortable in a fast-paced, resource-efficient environment. Desirable Experience in neurology, neurodegenerative disease, or rare disease clinical programs. Familiarity with risk-based monitoring (RBM), centralized monitoring, and ICH E6(R3) risk-proportionate approaches. Professional certification: RQAP-GCP (SQA), RAC (RAPS), CCRA (ACRP), or equivalent. Experience supporting NDA/BLA/MAA submissions and post-approval quality oversight. Knowledge of 21 CFR Part 11 / Annex 11 (computerized systems) and data integrity principles (ALCOA+). ## Location/Time Zones This is a full-time remote position in the East Coast US, Israel or Europe. Flexible schedule with frequent calls across Israel, North America and Europe time zones. Occasional travel including internationally within US and Europe required.", "summaryDescription" : "Director / Senior Director, GCP Quality Assurance Lead (US/IL/EU) at Prilenia Therapeutics. Skills: GCP Quality Assurance, Regulatory Inspections, QMS Development. Ensure trials comply with regulations. Serve as day-to-day QA lead", "postedDate" : "2026-06-08T21:02:53.077", "createdAt" : "2026-06-08T21:02:53.077", "lastUpdated" : "2026-06-16T05:35:40.085", "ingestTimestamp" : "2026-06-14T21:25:25.106", "mongoId" : "6a2c8e5474d8ee00a097ba6e", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 245000, "salaryAnnualMax" : 355000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "GCP", "GvP", "GLP", "ICH guidelines", "SOPs", "Protocol deviations", "Non-conformances", "CAPA", "EU GvP modules", "ICH E2 series", "ICH E6(R2/R3)", "Leadership", "GCP Quality Assurance", "Regulatory Inspections", "QMS Development", "Quality assurance", "Clinical development", "Regulatory affairs", "Drug safety", "Biostatistics", "Quality oversight", "Issue escalation", "CAPA resolution", "Inspection readiness", "Quality metrics", "Quality agreements", "Vendor quality", "Vendor support", "QMS lifecycle", "Regulatory intelligence", "Quality culture", "Professional development", "CAPA management", "Neurodegenerative diseases", "Neurodevelopmental disorders", "Huntington's Disease", "ALS", "Sigma-1 receptor agonist", "FDA regulations", "EU regulations", "OECD Principles of GLP", "Data integrity principles", "RQAP-GCP (SQA)", "RAC (RAPS)", "CCRA (ACRP)", "Veeva Vault", "Wingspan" ], "skillCount" : 47, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Director", "dataQualityScore" : 1.0, "_score" : 806.84155, "daysOld" : 7, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2a532674d8ee00a05fd09e", "title" : "Senior Manager, GCP Quality Assurance", "company" : "Olema Oncology", "industry" : "Biotechnology", "salary" : { "min" : 205000.0, "max" : 285000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Manager, GCP Quality Assurance in San Francisco, United States, adjusted for the biotech industry and manager-level experience." }, "location" : "San Francisco, California, United States", "locations" : [ "San Francisco", "California", "United States", "Boston", "Massachusetts", "United States" ], "timestamp" : "2026-06-14T19:27:42.236", "fingerprint" : "951720306d077bf855216b300280c7c242830b9754ed8353a82c76fd1d9766f6", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/olema/jobs/6014223004", "externalId" : "6014223004", "industryFunction" : { }, "structuredLocations" : [ { "city" : "San Francisco", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "37.7879363,-122.4075201" }, { "city" : "Cambridge", "state" : "Massachusetts", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "42.3656347,-71.1040018" } ], "locationText" : "San Francisco, California, United States; Cambridge, Massachusetts, United States", "experienceLevel" : "Manager", "technicalSkills" : "GCP, GVP, GLP", "professionalSkills" : [ "Quality Assurance", "Clinical trials", "Pharmacovigilance reporting", "Risk management", "Process improvement", "Quality Management System" ], "hardSkillsList" : [ "Audit preparation", "Audit execution", "Audit report preparation", "CAPA management", "SOP writing", "SOP review" ], "softSkillsList" : [ "Analytical thinker", "Problem-solving skills" ], "hardSkills" : [ { "name" : "Audit preparation", "level" : "intermediate" }, { "name" : "Audit execution", "level" : "intermediate" }, { "name" : "Audit report preparation", "level" : "intermediate" }, { "name" : "CAPA management", "level" : "intermediate" }, { "name" : "SOP writing", "level" : "intermediate" }, { "name" : "SOP review", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Analytical thinker" }, { "name" : "Problem-solving skills" } ], "majorSkills" : "GCP compliance, GVP compliance, Quality Assurance, Auditing", "majorSkillsList" : [ "GCP compliance", "GVP compliance", "Quality Assurance", "Auditing" ], "coreResponsibilities" : "Perform internal and external audits, Ensure GCP/GVP compliance, Assist in identifying clinical trial risks, Communicate clinical trial risks, Review study-related documents, Approve study-related documents, Support audits, Provide GCP/GVP auditing activities, Prepare audit reports, Follow up on findings/observations, Communicate audit results, Support regulatory authority inspections, Assist with GxP inspection readiness, Oversee quality aspects for clinical study start-up, Oversee quality aspects for clinical study execution, Oversee quality aspects for clinical study close-out, Provide leadership to staff, Provide guidance to staff, Provide direction to staff, Assist in preparation for health authority inspections, Assist in preparation for supplier inspections, Assist in preparation for clinical site inspections, Oversee clinical compliance, Oversee clinical quality, Improve Olema’s risk based GCP compliance approach, Refine Olema’s risk based GCP compliance approach, Support Quality Management System, Review deviations, Approve deviations, Review CAPAs, Approve CAPAs, Review change controls, Approve change controls, Draft policies, Review policies, Approve policies, Draft procedures, Review procedures, Approve procedures, Draft work instructions, Review work instructions, Approve work instructions", "teamCollaboration" : "Cross-functional study teams; Internal staff; External team members", "domainKnowledge" : "Clinical trials; Pharmacovigilance reporting; FDA regulations; EMA regulations; ICH guidelines; Good Clinical Practice; Good Pharmacovigilance Practice; Good Laboratory Practice", "domainList" : [ "clinical-trials", "pharmacovigilance-reporting", "fda-regulations", "ema-regulations", "ich-guidelines", "good-clinical-practice", "good-pharmacovigilance-practice", "good-laboratory-practice" ], "domainSpecificKnowledge" : [ "Clinical trials", "Pharmacovigilance reporting", "FDA regulations", "EMA regulations", "ICH guidelines", "Good Clinical Practice", "Good Pharmacovigilance Practice", "Good Laboratory Practice" ], "toolProficiency" : [ "Veeva systems" ], "communicationSkills" : "Verbal communication; Written communication", "documentationSkills" : "SOP writing; SOP review", "problemSolvingSkills" : "Problem-solving", "specialRequirements" : "2 days a week on site, Up to 25% travel", "qualificationsBasic" : "Bachelor's degree in scientific discipline, Minimum of 8 years of relevant experience in Quality Assurance or related role, Demonstrated experience leading and/or conducting internal and external QA audits, Demonstrated ability to develop and foster positive, collaborative relationships, Experience supporting regulatory agency inspections, Experience writing and reviewing SOPs, Knowledge and experience in GCP, Knowledge and experience in GVP", "qualificationsPreferred" : "Good Laboratory Practice (GLP) experience", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential. Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for our patients, for your career, for what’s beyond. You can view our latest corporate deck and other presentations here. About the Role >>> Senior Manager, GCP Clinical Quality As the Senior Manager, GCP Clinical Quality reporting to the Senior Director GCP Quality Assurance, you will be partnering with Clinical Development/Operations, Pharmacovigilance and Safety to actively participate in cross-functional study teams to ensure GCP/GVP compliance, assisting in identifying and communicating clinical trial-related risks and opportunities for process improvement as well as reviewing / approving study-related documents and plans and supporting audits. This hybrid role is based out of our San Francisco, CA or Cambridge, MA office requires 2 days a week on site and up to 25% travel. Your work will primarily encompass: Perform internal and external audits as assigned to ensure compliance with GCP/GVP regulations and guidelines Provide GCP/GVP auditing activities, including audit preparation, execution, report preparation, and follow-up to any findings/observations, including corrective and preventive actions (CAPAs), communicate audit results to internal stakeholders Provide a support role during regulatory authority inspections and assist with GxP inspection readiness activities Oversee quality aspects related to clinical study start-up, execution, and close-out by providing leadership, guidance, and direction to staff consistent with GCP/GVP Assist in preparation for health authority inspections, suppliers and/or clinical sites Oversee clinical compliance and quality within the context of cross-functional study teams Continue to improve/refine Olema’s risk based GCP compliance approach globally Support Quality Management System (QMS) including, but not be limited to, the following activities: QA review/approval of deviations, CAPAs and change controls Draft, review, and approve policies, procedures and work instructions Ideal Candidate Profile >>> Key Requirements A love of challenging, important work. We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All employees within our company play a unique and crucial role in our success, both in accomplishing our mission and building a positive company culture. As such, we are looking for someone with the right combination of knowledge, experience, and attributes for this role. Knowledge: Bachelor’s degree in scientific discipline Strong understanding of clinical trials and pharmacovigilance reporting Strong understanding of FDA, EMA, and ICH Health compliance requirements Understanding of industry quality management tools, quality systems (e.g., QMS, eTMF, EMRs, EDC, etc.). Experience: Minimum of 8 years of relevant experience in Quality Assurance or related role in a pharmaceutical, biotechnology, or related environment Demonstrated experience leading and/or conducting internal and external QA audits developing and executing risk-based audit plans Demonstrated ability to develop and foster positive, collaborative relationships with internal staff as well as with external, third-party vendors Experience supporting regulatory agency inspections Experience writing and reviewing SOPs Experience using QMS (Veeva systems preferred) Knowledge and experience in Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP) regulations. In addition, preferred Good Laboratory Practice (GLP) experience Attributes: Excellent verbal and written communication skills Ability to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines Excellent planning, organization, and time management skills including the ability to support and prioritize multiple projects The base pay range for this position is expected to be $160,000 - $180,000 annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits. #LI-CK1 Important Information >>> We provide equal opportunity to all employees and applicants for employment and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated. We offer a competitive compensation and benefits package, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants. Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you. Fraud Alert: We are aware of employment scams where individuals pose as representatives of Olema Oncology and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is olema.com; our careers page is olema.com/careers; our LinkedIn page is linkedin.com/company/olema-oncology. Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments of any kind, and does not make job offers without an in-person interview.", "summaryDescription" : "Senior Manager, GCP Quality Assurance at Olema Oncology. Skills: GCP compliance, GVP compliance, Quality Assurance, Auditing. Perform internal and external audits. Ensure GCP/GVP compliance", "postedDate" : "2026-06-11T22:09:04.883", "createdAt" : "2026-06-11T22:09:04.883", "lastUpdated" : "2026-06-14T19:27:42.236", "ingestTimestamp" : "2026-06-11T22:09:04.883", "mongoId" : "6a2a532674d8ee00a05fd09e", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 205000, "salaryAnnualMax" : 285000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Audit preparation", "Audit execution", "Audit report preparation", "CAPA management", "SOP writing", "SOP review", "Analytical thinker", "Problem-solving skills", "GCP compliance", "GVP compliance", "Quality Assurance", "Auditing", "Clinical trials", "Pharmacovigilance reporting", "Risk management", "Process improvement", "Quality Management System", "FDA regulations", "EMA regulations", "ICH guidelines", "Good Clinical Practice", "Good Pharmacovigilance Practice", "Good Laboratory Practice", "Veeva systems" ], "skillCount" : 24, "jobCategory" : "other", "jobSubcategory" : "clinical", "dataQualityScore" : 0.8888889, "_score" : 802.27747, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotechnology" }, { "id" : "6a305117f292fd229cef94f5", "title" : "Senior Director", "company" : "Pediatrics Plus", "salary" : { "min" : 75000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Russellville, Arkansas, United States", "locations" : [ "Russellville", "Arkansas", "United States" ], "timestamp" : "2026-06-16T10:38:44.775", "fingerprint" : "2f4587ee5c088ab5aaa3e33a303b7c87c91f8c76cae95aed276607c5ae6658dc", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/indeedbtrbt/jobs/4689381006", "externalId" : "4689381006", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Russellville", "state" : "Arkansas", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "35.2784173,-93.1337856" } ], "locationText" : "Russellville, Arkansas, United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Do you have a heart and passion for leadership? Pediatrics Plus is a specialized pediatric healthcare provider. We are committed to helping children succeed in all stages of life through evidence-based therapy and education, diagnostic services, state of the art facilities, specialized equipment, family support, and community investment. We are currently looking for qualified individuals to fill the position of Senior Director! This role is responsible for providing strategic leadership to the developmental preschool program, therapy, and ABA programs at the site, building Pediatrics Plus culture, and ensuring excellence in service. The Senior Director oversees all aspects of the site operations including preschool and therapy enrollment, leadership of team members, management of systems and processes at the site level, compliance to all state-mandated guidelines, revenue/expenses, and health and safety. What we offer: Competitive Pay Bonus Program Paid Time Off Medical, Dental, a collaborative environment between teachers, therapists, and other team members; and with a high priority placed on family engagement and involvement. Oversee all aspects of staff management including hiring, terminations, corrective actions, performance reviews, position placements, promotions, and training. Ensures approval from Regional Leader and Legal for terminations based on company violations other than occurrence policy violation. Oversee all annual themes ensuring they are actively promoted and reinforced following directions provided from senior leadership. Ensure compliance through Arkansas Childcare Licensing, AR Medicaid EIDT, governing agencies, audits, and any additional compliance requests by the organization. Provide oversight and leadership to staff management to promote leadership growth and site development. This includes weekly or bi-weekly one-on-one meetings with: Therapy Director Developmental Preschool Director BCBA Team Leads Administrative Team Lead Nurse. Provide oversight and compliance with all aspects of the preschool and therapy budget including revenue, expenses, and payroll within the parameters of the site’s projections. Oversee the developmental preschool enrollment and therapy caseload management. Make decisions and oversee the discharge process for children attending the preschool and/or therapy. Maintain quality assurance through measures provided by Pediatrics Plus administration. Ensure that all human resource functions (payroll, time-off requests, worker’s compensation, leaves of absences, and any needed paperwork) are completed accurately and timely and that adequate communication is maintained with the Human Resources Department. Oversee and handle site-related people issues including but not limited to coaching, written warnings, development plans, and termination with approval from designated leadership. Attend and represent site in designated organizational, leadership, and clinical program line meetings. Assist with marketing events, doctor visits, and other marketing avenues as needed and/or requested. Responsible for handling any parent complaints or concerns and escalating if warranted to appropriate leadership. Ensure completion of site metrics to understand current status and possible need to increase numbers to set targets. Attend local business functions and have a working relationship with other businesses, local inﬂuencers, mom/parent groups, churches, and chambers within the community. Demonstrate an understanding of the local Lead program, its impact at the site level, and serves as a representative at meetings. Participates in one-on-one meetings with leader. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. What you have: Ability to read, analyze, and interpret general business data, professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and policy procedure manuals. Ability to effectively present information and respond to questions from groups of executives, managers, physicians, clients, customers, field clinicians, and the public. Knowledge of various funding source guidelines. Ability to communicate effectively and professionally with a wide variety of people. Must be able to work with children birth to age 21 and families who are at risk. Ability to function independently in all aspects, including project identification, evaluation, contract negotiations, and coordination with management and internal departments. Strong organizational skills with attention to detail and accuracy. Ability to handle multiple tasks in a very busy environment. Basic computer skills which include a working knowledge of keyboarding, database, word processing, spreadsheet, and Internet software. Ability to represent the company in a confident, persuasive, and positive manner. Excellent interpersonal, verbal, and written communication skills. Ability to work under stress and respond quickly in emergency situations. In-depth knowledge of operational, clinical and referral development systems. Ability to work effectively within a complex matrix organization. Reports for work dressed appropriately and complies with company policies regarding dress code. Ability to maintain regular and punctual attendance. Ability to complete tasks in a timely manner. Travel may be required. Minimum Qualifications: Bachelor’s Degree from an accredited university. Degree in Early Childhood Education, Elementary Education, Early Childhood Special Education, or therapy related field, preferred. Minimum three years of successful experience in a classroom setting working with developmentally at-risk children and/or broad clinical experience, preferred. Physical Demands: While performing the duties of this job, the employee is frequently required to accurately communicate information and ideas so others will understand through sight and hearing. The employee is regularly required to move including walking, running, jumping, and sitting. The employee is regularly required to use hands and fingers to handle, lift, reach, and feel. The employee is frequently required to stand and stoop, twist, bend, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 50 pounds. Specific vision abilities required by this job include near and distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. We are an equal opportunity employer and prohibit discrimination/harassment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. #IND456 Full Time Compensation starts at: $75,000 annually", "summaryDescription" : "Senior Director at Pediatrics Plus", "postedDate" : "2026-06-15T23:15:37.151", "createdAt" : "2026-06-15T23:15:37.151", "lastUpdated" : "2026-06-16T10:38:44.775", "ingestTimestamp" : "2026-06-15T23:15:37.151", "mongoId" : "6a305117f292fd229cef94f5", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 75000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 797.9697, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2a532674d8ee00a05fd09d", "title" : "Senior Manager, GCP Quality Assurance", "company" : "Olema Oncology", "industry" : "Biotechnology", "salary" : { "min" : 215000.0, "max" : 295000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Biotech industry in San Francisco, adjusted for Senior Manager level and full-time employment." }, "location" : "San Francisco, California, United States", "locations" : [ "San Francisco", "California", "United States", "Boston", "Massachusetts", "United States" ], "timestamp" : "2026-06-13T22:47:42.386", "fingerprint" : "cffb8ed050b2e527c2c2fce15714bffeaa0e886cb51bf55fb7f390cb65f3e2b0", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/olema/jobs/6014222004", "externalId" : "6014222004", "industryFunction" : { }, "structuredLocations" : [ { "city" : "San Francisco", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "37.7879363,-122.4075201" }, { "city" : "Cambridge", "state" : "Massachusetts", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "42.3656347,-71.1040018" } ], "locationText" : "San Francisco, California, United States; Cambridge, Massachusetts, United States", "experienceLevel" : "Manager", "technicalSkills" : "GCP, GVP, GLP", "professionalSkills" : [ "Quality Assurance", "Clinical trials", "Pharmacovigilance reporting", "Risk management", "Process improvement", "Quality Management System" ], "hardSkillsList" : [ "Audit preparation", "Audit execution", "Report preparation", "CAPA management", "SOP writing" ], "softSkillsList" : [ "Analytical thinker", "Problem-solving skills" ], "hardSkills" : [ { "name" : "Audit preparation", "level" : "intermediate" }, { "name" : "Audit execution", "level" : "intermediate" }, { "name" : "Report preparation", "level" : "intermediate" }, { "name" : "CAPA management", "level" : "intermediate" }, { "name" : "SOP writing", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Analytical thinker" }, { "name" : "Problem-solving skills" } ], "majorSkills" : "GCP compliance, GVP compliance, Quality Assurance, Auditing", "majorSkillsList" : [ "GCP compliance", "GVP compliance", "Quality Assurance", "Auditing" ], "coreResponsibilities" : "Perform internal and external audits, Ensure GCP/GVP compliance, Provide GCP/GVP auditing activities, Communicate audit results, Support regulatory authority inspections, Assist with GxP inspection readiness, Oversee quality aspects, Provide leadership, guidance, and direction, Assist in preparation for inspections, Oversee clinical compliance and quality, Improve/refine risk based GCP compliance, Support Quality Management System, QA review/approval of deviations, QA review/approval of CAPAs, QA review/approval of change controls, Draft policies, Review policies, Approve policies, Draft procedures, Review procedures, Approve procedures, Draft work instructions, Review work instructions, Approve work instructions", "teamCollaboration" : "Cross-functional study teams; Internal staff; External team members", "domainKnowledge" : "Clinical trials; Pharmacovigilance reporting; FDA regulations; EMA regulations; ICH guidelines; Quality systems; Good Clinical Practice; Good Pharmacovigilance Practice", "domainList" : [ "clinical-trials", "pharmacovigilance-reporting", "fda-regulations", "ema-regulations", "ich-guidelines", "quality-systems", "good-clinical-practice", "good-pharmacovigilance-practice" ], "domainSpecificKnowledge" : [ "Clinical trials", "Pharmacovigilance reporting", "FDA regulations", "EMA regulations", "ICH guidelines", "Quality systems", "Good Clinical Practice", "Good Pharmacovigilance Practice" ], "toolProficiency" : [ "Veeva systems" ], "communicationSkills" : "Verbal communication; Written communication", "documentationSkills" : "Review study-related documents; Approve study-related documents; Writing SOPs; Reviewing SOPs", "problemSolvingSkills" : "Problem-solving skills", "specialRequirements" : "2 days a week on site, Up to 25% travel", "qualificationsBasic" : "Bachelor's degree in scientific discipline, Minimum of 8 years of relevant experience, Demonstrated experience leading audits, Demonstrated ability to develop relationships, Experience supporting regulatory agency inspections, Experience writing and reviewing SOPs, Knowledge and experience in GCP, Knowledge and experience in GVP", "qualificationsPreferred" : "Good Laboratory Practice (GLP) experience", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential. Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for our patients, for your career, for what’s beyond. You can view our latest corporate deck and other presentations here. About the Role >>> Senior Manager, GCP Clinical Quality As the Senior Manager, GCP Clinical Quality reporting to the Senior Director GCP Quality Assurance, you will be partnering with Clinical Development/Operations, Pharmacovigilance and Safety to actively participate in cross-functional study teams to ensure GCP/GVP compliance, assisting in identifying and communicating clinical trial-related risks and opportunities for process improvement as well as reviewing / approving study-related documents and plans and supporting audits. This hybrid role is based out of our San Francisco, CA or Cambridge, MA office requires 2 days a week on site and up to 25% travel. Your work will primarily encompass: Perform internal and external audits as assigned to ensure compliance with GCP/GVP regulations and guidelines Provide GCP/GVP auditing activities, including audit preparation, execution, report preparation, and follow-up to any findings/observations, including corrective and preventive actions (CAPAs), communicate audit results to internal stakeholders Provide a support role during regulatory authority inspections and assist with GxP inspection readiness activities Oversee quality aspects related to clinical study start-up, execution, and close-out by providing leadership, guidance, and direction to staff consistent with GCP/GVP Assist in preparation for health authority inspections, suppliers and/or clinical sites Oversee clinical compliance and quality within the context of cross-functional study teams Continue to improve/refine Olema’s risk based GCP compliance approach globally Support Quality Management System (QMS) including, but not be limited to, the following activities: QA review/approval of deviations, CAPAs and change controls Draft, review, and approve policies, procedures and work instructions Ideal Candidate Profile >>> Key Requirements A love of challenging, important work. We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All employees within our company play a unique and crucial role in our success, both in accomplishing our mission and building a positive company culture. As such, we are looking for someone with the right combination of knowledge, experience, and attributes for this role. Knowledge: Bachelor’s degree in scientific discipline Strong understanding of clinical trials and pharmacovigilance reporting Strong understanding of FDA, EMA, and ICH Health compliance requirements Understanding of industry quality management tools, quality systems (e.g., QMS, eTMF, EMRs, EDC, etc.). Experience: Minimum of 8 years of relevant experience in Quality Assurance or related role in a pharmaceutical, biotechnology, or related environment Demonstrated experience leading and/or conducting internal and external QA audits developing and executing risk-based audit plans Demonstrated ability to develop and foster positive, collaborative relationships with internal staff as well as with external, third-party vendors Experience supporting regulatory agency inspections Experience writing and reviewing SOPs Experience using QMS (Veeva systems preferred) Knowledge and experience in Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP) regulations. In addition, preferred Good Laboratory Practice (GLP) experience Attributes: Excellent verbal and written communication skills Ability to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines Excellent planning, organization, and time management skills including the ability to support and prioritize multiple projects The base pay range for this position is expected to be $160,000 - $180,000 annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits. #LI-CK1 Important Information >>> We provide equal opportunity to all employees and applicants for employment and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated. We offer a competitive compensation and benefits package, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants. Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you. Fraud Alert: We are aware of employment scams where individuals pose as representatives of Olema Oncology and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is olema.com; our careers page is olema.com/careers; our LinkedIn page is linkedin.com/company/olema-oncology. Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments of any kind, and does not make job offers without an in-person interview.", "summaryDescription" : "Senior Manager, GCP Quality Assurance at Olema Oncology. Skills: GCP compliance, GVP compliance, Quality Assurance, Auditing. Perform internal and external audits. Ensure GCP/GVP compliance", "postedDate" : "2026-06-11T21:09:50.262", "createdAt" : "2026-06-11T21:09:50.262", "lastUpdated" : "2026-06-13T22:47:42.386", "ingestTimestamp" : "2026-06-11T21:09:50.262", "mongoId" : "6a2a532674d8ee00a05fd09d", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 215000, "salaryAnnualMax" : 295000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Audit preparation", "Audit execution", "Report preparation", "CAPA management", "SOP writing", "Analytical thinker", "Problem-solving skills", "GCP compliance", "GVP compliance", "Quality Assurance", "Auditing", "Clinical trials", "Pharmacovigilance reporting", "Risk management", "Process improvement", "Quality Management System", "FDA regulations", "EMA regulations", "ICH guidelines", "Quality systems", "Good Clinical Practice", "Good Pharmacovigilance Practice", "Veeva systems" ], "skillCount" : 23, "jobCategory" : "other", "jobSubcategory" : "clinical", "dataQualityScore" : 0.8888889, "_score" : 796.9564, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotechnology" }, { "id" : "6a3076edf292fd229c020180", "title" : "Senior Director", "company" : "Pediatrics Plus", "salary" : { "min" : 175000.0, "max" : 250000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Director in Healthcare in Russellville, United States, adjusted for seniority and industry." }, "location" : "Russellville, Arkansas, United States", "locations" : [ "Russellville", "Arkansas", "United States" ], "timestamp" : "2026-06-16T08:33:47.123", "fingerprint" : "7f51926a089e99d0822a5ddc4ca1cc4b58c361f403bbbed4022497b2abc67b79", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/pediatricsplus/jobs/4689382006", "externalId" : "4689382006", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Russellville", "state" : "Arkansas", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "35.2784173,-93.1337856" } ], "locationText" : "Russellville, Arkansas, United States", "minimumEducation" : "Bachelor's", "experienceLevel" : "Director", "remoteFriendly" : false, "rawDescription" : "Do you have a heart and passion for leadership? Pediatrics Plus is a specialized pediatric healthcare provider. We are committed to helping children succeed in all stages of life through evidence-based therapy and education, diagnostic services, state of the art facilities, specialized equipment, family support, and community investment. We are currently looking for qualified individuals to fill the position of Senior Director! This role is responsible for providing strategic leadership to the developmental preschool program, therapy, and ABA programs at the site, building Pediatrics Plus culture, and ensuring excellence in service. The Senior Director oversees all aspects of the site operations including preschool and therapy enrollment, leadership of team members, management of systems and processes at the site level, compliance to all state-mandated guidelines, revenue/expenses, and health and safety. What we offer: Competitive Pay Bonus Program Paid Time Off Medical, Dental, a collaborative environment between teachers, therapists, and other team members; and with a high priority placed on family engagement and involvement. Oversee all aspects of staff management including hiring, terminations, corrective actions, performance reviews, position placements, promotions, and training. Ensures approval from Regional Leader and Legal for terminations based on company violations other than occurrence policy violation. Oversee all annual themes ensuring they are actively promoted and reinforced following directions provided from senior leadership. Ensure compliance through Arkansas Childcare Licensing, AR Medicaid EIDT, governing agencies, audits, and any additional compliance requests by the organization. Provide oversight and leadership to staff management to promote leadership growth and site development. This includes weekly or bi-weekly one-on-one meetings with: Therapy Director Developmental Preschool Director BCBA Team Leads Administrative Team Lead Nurse. Provide oversight and compliance with all aspects of the preschool and therapy budget including revenue, expenses, and payroll within the parameters of the site’s projections. Oversee the developmental preschool enrollment and therapy caseload management. Make decisions and oversee the discharge process for children attending the preschool and/or therapy. Maintain quality assurance through measures provided by Pediatrics Plus administration. Ensure that all human resource functions (payroll, time-off requests, worker’s compensation, leaves of absences, and any needed paperwork) are completed accurately and timely and that adequate communication is maintained with the Human Resources Department. Oversee and handle site-related people issues including but not limited to coaching, written warnings, development plans, and termination with approval from designated leadership. Attend and represent site in designated organizational, leadership, and clinical program line meetings. Assist with marketing events, doctor visits, and other marketing avenues as needed and/or requested. Responsible for handling any parent complaints or concerns and escalating if warranted to appropriate leadership. Ensure completion of site metrics to understand current status and possible need to increase numbers to set targets. Attend local business functions and have a working relationship with other businesses, local inﬂuencers, mom/parent groups, churches, and chambers within the community. Demonstrate an understanding of the local Lead program, its impact at the site level, and serves as a representative at meetings. Participates in one-on-one meetings with leader. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. What you have: Ability to read, analyze, and interpret general business data, professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and policy procedure manuals. Ability to effectively present information and respond to questions from groups of executives, managers, physicians, clients, customers, field clinicians, and the public. Knowledge of various funding source guidelines. Ability to communicate effectively and professionally with a wide variety of people. Must be able to work with children birth to age 21 and families who are at risk. Ability to function independently in all aspects, including project identification, evaluation, contract negotiations, and coordination with management and internal departments. Strong organizational skills with attention to detail and accuracy. Ability to handle multiple tasks in a very busy environment. Basic computer skills which include a working knowledge of keyboarding, database, word processing, spreadsheet, and Internet software. Ability to represent the company in a confident, persuasive, and positive manner. Excellent interpersonal, verbal, and written communication skills. Ability to work under stress and respond quickly in emergency situations. In-depth knowledge of operational, clinical and referral development systems. Ability to work effectively within a complex matrix organization. Reports for work dressed appropriately and complies with company policies regarding dress code. Ability to maintain regular and punctual attendance. Ability to complete tasks in a timely manner. Travel may be required. Minimum Qualifications: Bachelor’s Degree from an accredited university. Degree in Early Childhood Education, Elementary Education, Early Childhood Special Education, or therapy related field, preferred. Minimum three years of successful experience in a classroom setting working with developmentally at-risk children and/or broad clinical experience, preferred. Physical Demands: While performing the duties of this job, the employee is frequently required to accurately communicate information and ideas so others will understand through sight and hearing. The employee is regularly required to move including walking, running, jumping, and sitting. The employee is regularly required to use hands and fingers to handle, lift, reach, and feel. The employee is frequently required to stand and stoop, twist, bend, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 50 pounds. Specific vision abilities required by this job include near and distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. We are an equal opportunity employer and prohibit discrimination/harassment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.", "summaryDescription" : "Senior Director at Pediatrics Plus", "postedDate" : "2026-06-16T01:19:32.996", "createdAt" : "2026-06-16T01:19:32.996", "lastUpdated" : "2026-06-16T08:33:47.123", "ingestTimestamp" : "2026-06-16T01:19:32.996", "mongoId" : "6a3076edf292fd229c020180", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 175000, "salaryAnnualMax" : 250000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Director", "dataQualityScore" : 0.7777778, "_score" : 790.82996, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a305611f292fd229cf24978", "title" : "Associate Director, Quality Control", "company" : "Moderna", "salary" : { "min" : 175000.0, "max" : 250000.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Biotech industry in Canada, adjusted for Director seniority and company size." }, "location" : "Canada", "locations" : [ "Canada" ], "timestamp" : "2026-06-16T13:07:21.885", "fingerprint" : "f893ce06841cc35748bcc2ca2aa28fb59f13e05d0776347a0bfc6bdc0aa46e83", "source" : "workday", "language" : "fr", "applyUrl" : "https://modernatx.wd1.myworkdayjobs.com/M_tx/job/Laval---Canada/Associate-Director--Quality-Control_R19304", "externalId" : "R19304", "industryFunction" : { }, "locationPoint" : "56.1304,-106.3468", "structuredLocations" : [ { "country" : "Canada", "continent" : "na", "workMode" : "onsite" } ], "locationText" : "Canada", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "remoteFriendly" : true, "rawDescription" : "**Le poste** Se joindre à Moderna, c’est faire progresser la science de l’ARNm pour transformer la médecine. Travaillez avec des équipes mondiales exceptionnelles sur un vaste portefeuille de programmes et bâtissez une carrière qui fait une réelle différence pour les patients. À Laval, le partenariat à long terme de Moderna avec le gouvernement du Canada renforce la préparation du pays face aux pandémies. Notre installation de fabrication de vaccins à ARNm permettra un accès rapide à des vaccins respiratoires produits au pays. Grâce au développement des talents locaux et à la collaboration en recherche, nous bâtissons un solide écosystème de l’ARNm au Canada. Joignez-vous à nous pour façonner l’avenir de la biotechnologie et de l’innovation en santé. Vous jouerez un rôle déterminant dans la création, le développement et l’exploitation d’une organisation de Contrôle de la qualité de calibre mondial au sein du site manufacturier de Moderna à Laval. En assurant le leadership stratégique et opérationnel des activités QC soutenant la fabrication commerciale, vous contribuerez directement à la qualité, à la conformité et à la disponibilité de médicaments innovants destinés aux patients. À la croisée des opérations, de la science analytique et de la qualité, vous dirigerez la mise en place et la préparation opérationnelle des laboratoires de Contrôle de la qualité soutenant les essais de substance active et de produit fini. Vous superviserez les essais analytiques, la microbiologie, la surveillance environnementale, la surveillance des utilités critiques, les programmes de stabilité et les activités de libération, tout en assurant l’excellence opérationnelle au sein des laboratoires internes et des réseaux externes de fabrication et d’essais. Ce poste offre une occasion unique de travailler dans un environnement hautement innovant où les technologies numériques, l’automatisation des laboratoires, l’analytique avancée et les outils d’intelligence artificielle générative contribuent à renforcer la performance, l’intégrité des données, la prise de décision et l’amélioration continue des opérations qualité. **Voici ce que vous ferez** * Assurer le leadership stratégique et opérationnel des activités de Contrôle de la qualité soutenant la fabrication commerciale, la gestion du cycle de vie des produits, les opérations de laboratoire et la supervision des partenaires externes. * Diriger les opérations de Contrôle de la qualité soutenant les essais des matières premières, en cours de procédé, de substance active, de produit fini, la microbiologie, la surveillance environnementale, les essais de libération et les programmes de stabilité. * Superviser la mise en place et la préparation opérationnelle des laboratoires de Contrôle de la qualité soutenant les essais de substance active et de produit fini. * Diriger les activités de préparation des installations et des laboratoires, la mise en œuvre des systèmes de laboratoire, les transferts de méthodes, les activités de qualification et de validation ainsi que l’établissement d’opérations d’essais conformes. * Assurer la prestation de services de contrôle de la qualité conformes, fiables et en temps opportun. * Assurer la supervision stratégique des laboratoires internes et des partenaires d’essais externes, incluant les organismes de fabrication sous contrat (CMO), les laboratoires d’essais sous contrat (CTL) et les autres fournisseurs de services. * Agir comme principal représentant du Contrôle de la qualité et expert(e) (SME) au sein des équipes transversales en assurant l’alignement entre Fabrication, AS&T, Assurance qualité, Affaires réglementaires, Ingénierie, Chaîne d’approvisionnement et Contrôle de la qualité global. * Assurer la supervision stratégique des programmes de surveillance environnementale et des utilités critiques afin de soutenir les opérations manufacturières et la qualité des produits. * Maintenir des stratégies robustes de contrôle de la contamination et assurer la conformité réglementaire, l’analyse des tendances, la gestion des enquêtes et l’amélioration continue. * Assurer la livraison rapide des résultats d’essais ainsi que la gestion efficace des écarts, des enquêtes OOS/OOT, des CAPA, des contrôles de changements et des dossiers du système qualité. * Maintenir la supervision des systèmes qualité, des enquêtes, de l’intégrité des données et des initiatives d’amélioration continue. * Diriger et soutenir les transferts de méthodes analytiques, les qualifications, les validations et la mise en œuvre des changements analytiques soutenant les produits commerciaux et les nouveaux produits. * Réviser et approuver les méthodes analytiques, spécifications, protocoles, rapports, documents de stabilité et autres enregistrements cGMP. * Piloter des initiatives d’amélioration continue visant l’efficacité des laboratoires, l’excellence opérationnelle, l’intégrité des données et la préparation aux inspections. * Établir et superviser les indicateurs de performance QC, les programmes d’analytique, de surveillance et de tendances afin de soutenir la robustesse des procédés et la qualité des produits. * Collaborer avec les équipes Digital et TI afin de renforcer les systèmes de laboratoire, les stratégies d’automatisation et la gouvernance des données. * Tirer parti des outils numériques avancés, de l’automatisation et des opportunités émergentes liées à l’intelligence artificielle et à l’IA générative afin d’améliorer l’efficacité opérationnelle, l’analyse des données et les capacités décisionnelles. * Diriger des enquêtes techniques complexes et fournir une expertise scientifique permettant de résoudre des enjeux analytiques, opérationnels et de conformité. * Développer, mettre en œuvre et maintenir les procédures de laboratoire, les programmes de formation et les systèmes opérationnels nécessaires au maintien d’une conformité cGMP durable. * Soutenir les transferts de technologie, les transferts de procédés, les campagnes PPQ, les introductions de nouveaux produits, les programmes de stabilité et les activités de gestion du cycle de vie des produits. * Soutenir les soumissions réglementaires, les Revues annuelles de qualité produit (APQR) et les activités liées au portefeuille commercial. * Représenter le Contrôle de la qualité lors des inspections réglementaires, inspections des autorités de santé, audits clients, audits fournisseurs et audits internes. * Maintenir un état constant de préparation aux inspections et assurer la conformité aux exigences réglementaires mondiales. * Respecter l’ensemble des réglementations GxP, lignes directrices et politiques d’entreprise applicables. * Exécuter les activités conformément aux procédures opérationnelles normalisées (SOP), aux instructions de travail et aux documents directeurs internes. * Assurer le respect des Bonnes pratiques de documentation et des exigences d’intégrité des données. * Compléter les formations requises conformément aux échéanciers établis et aux exigences de requalification. * Contribuer à la stratégie du département, à la planification des ressources et à la gestion budgétaire afin de soutenir les objectifs organisationnels et la croissance future. * Diriger, développer, coacher et mobiliser les équipes de Contrôle de la qualité. * Superviser la gestion du rendement, le mentorat, le développement de carrière et la progression professionnelle du personnel de laboratoire. * Définir des objectifs clairs, des attentes mesurables et assurer le suivi de leur exécution. * Fournir conseils, orientation et soutien aux employé(e)s conformément aux stratégies et priorités de l’organisation. * Inspirer et motiver les membres de l’équipe afin qu’ils atteignent leur plein potentiel. * Mettre en place des plans de relève et des plans de développement des talents. * Identifier et désigner des remplaçants appropriés afin d’assurer la continuité des activités. * Favoriser une culture positive, inclusive et collaborative axée sur l’innovation, la responsabilisation et l’amélioration continue. * Agir comme liaison interdépartementale auprès d’AS&T, du Contrôle de la qualité global, du Contrôle de la qualité externe, de l’Assurance qualité, des Affaires réglementaires et des autres fonctions clés de l’organisation. **Les principaux Mindsets Moderna nécessaires pour réussir dans ce rôle :** • « Nous sommes obsédés par l’apprentissage. Nous n’avons pas besoin d’être les plus intelligents, mais d’apprendre le plus rapidement possible. » • « Nous numérisons partout où cela est possible en utilisant la puissance du code afin de maximiser notre impact pour les patients. » **Voici ce dont vous aurez besoin (Qualifications de base)** • Baccalauréat dans une discipline scientifique pertinente (sciences de la vie, biotechnologie, chimie, microbiologie, biochimie ou domaine connexe) ; diplôme supérieur souhaité. • Minimum de 10 ans d’expérience en Contrôle de la qualité dans un environnement commercial cGMP biotechnologique ou pharmaceutique, incluant une expérience de soutien aux opérations internes et externes de fabrication et d’essais. • Minimum de 4 à 6 ans d’expérience en leadership, incluant la gestion d’équipes techniques, d’opérations de laboratoire, de gestion de projets et de développement des talents. • Solide connaissance pratique des exigences réglementaires mondiales et des normes de l’industrie, incluant FDA, Santé Canada, EMA, ICH, ISPE, ASTM et les réglementations GxP applicables. • Expérience démontrée en essais analytiques, transferts de méthodes, qualification, validation et gestion du cycle de vie des méthodes au sein de l’industrie biotechnologique ou pharmaceutique. • Expertise avérée en Systèmes qualité, incluant la gestion des écarts, les enquêtes OOS/OOT, les CAPA, les contrôles de changements, les évaluations de risques et les programmes d’intégrité des données. • Ce poste est basé sur site et exige une présence à temps plein sur le site de Moderna. Ce poste n’est pas admissible au télétravail. • Dans le cadre de l’engagement de Moderna à bâtir une main-d’œuvre durable, un minimum de 2 ans d’autorisation de travail est requis pour ce poste. **Voici ce que vous apporterez (Qualifications souhaitées)** • Solide connaissance et expérience en surveillance environnementale, stratégies de contrôle de la contamination et programmes de surveillance des utilités critiques dans des environnements de fabrication biotechnologiques ou pharmaceutiques réglementés GMP, incluant les exigences réglementaires, l’analyse de données, les enquêtes et la préparation aux inspections. • Expérience de soutien aux inspections réglementaires, aux interactions avec les autorités de santé, aux audits clients, aux audits fournisseurs et aux activités de préparation aux inspections. • Solide connaissance des opérations de laboratoire soutenant la chimie, la microbiologie, les bioessais, la surveillance environnementale et les programmes de stabilité. • Une expérience de gestion d’activités de contrôle de la qualité auprès de CMO, CTL et partenaires externes est fortement souhaitée. • Succès démontré dans la direction de projets analytiques complexes, d’enquêtes, d’améliorations de procédés et d’initiatives transversales dans un environnement dynamique. • Solides compétences en rédaction technique et en documentation, incluant la révision et l’approbation de méthodes analytiques, protocoles, rapports, spécifications et documentation réglementaire. • Maîtrise des systèmes de laboratoire et d’entreprise tels que LIMS, SAP, LMS, systèmes électroniques de gestion de la qualité et outils d’analytique de données. • Expérience avec l’instrumentation de laboratoire et les plateformes logicielles, incluant des technologies chromatographiques et analytiques, souhaitée. • Excellentes compétences en leadership, relations interpersonnelles, communication et gestion des parties prenantes, avec la capacité d’influencer et de collaborer efficacement à tous les niveaux de l’organisation et avec des partenaires externes. • Capacité démontrée à penser de manière stratégique, à résoudre des problèmes complexes, à gérer des priorités multiples et à naviguer dans l’ambiguïté dans un environnement dynamique et matriciel. • Forte adhésion à l’excellence opérationnelle, à l’amélioration continue, à l’innovation et à la promotion d’une culture de conformité, de responsabilisation et d’esprit d’équipe. • Maîtrise de l’anglais, à l’écrit comme à l’oral ; d’autres langues constituent un atout. • Envie d’avoir un impact au sein d’une entreprise en forte croissance et en transformation, qui est Audacieuse, Tenace, Curieuse et Collaborative. **The Role:** Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. As Moderna continues to expand its manufacturing capabilities in Canada, this role will play a pivotal leadership position in establishing and operating a world-class Quality Control organization supporting commercial manufacturing operations in Laval. This individual will provide both strategic direction and hands-on operational leadership across analytical testing, microbiology, environmental monitoring, critical utilities monitoring, release testing, and stability programs while ensuring the highest standards of quality, compliance, and inspection readiness. The successful candidate will lead the startup and operational readiness of Quality Control laboratories supporting drug substance and drug product testing, building robust laboratory systems, driving method transfers and validation activities, and creating sustainable testing operations capable of supporting Moderna’s expanding commercial manufacturing network and future product portfolio. Working across internal and external networks, this leader will serve as a critical partner to Manufacturing, Analytical Science & Technology, Quality Assurance, Regulatory Affairs, Engineering, Supply Chain, Global Quality Control, Contract Manufacturing Organizations (CMOs), and Contract Testing Laboratories (CTLs). This is a unique opportunity to help shape the future of Quality Control operations within a highly innovative manufacturing environment while leveraging advanced digital capabilities, laboratory automation, data analytics, and emerging AI-enabled technologies to enhance operational excellence, data integrity, and decision-making. **Here 's What You'll Do:** * Provide strategic and operational leadership for Quality Control activities supporting commercial manufacturing, product lifecycle management, laboratory operations, and external partner oversight. * Lead Quality Control operations supporting raw material, in-process, drug substance, drug product, microbiology, environmental monitoring, release, and stability testing activities. * Oversee the startup, qualification, and operational readiness of Quality Control laboratories supporting commercial manufacturing. * Lead facility and laboratory readiness activities, implementation of laboratory systems, method transfers, qualification programs, validation activities, and establishment of compliant laboratory operations. * Ensure delivery of compliant, reliable, and timely Quality Control services across internal laboratories and external testing networks. * Provide strategic oversight of internal laboratories and external testing partners including CMOs, CTLs, and other third-party service providers. * Serve as the primary Quality Control representative and subject matter expert for cross-functional teams, ensuring strong alignment across Manufacturing, Analytical Science & Technology, Quality Assurance, Regulatory Affairs, Supply Chain, Engineering, and Global Quality Control. * Provide strategic oversight of Environmental Monitoring and Critical Utilities Monitoring programs, ensuring effective contamination control strategies, regulatory compliance, data trending, investigation management, and continuous improvement. * Establish and maintain robust contamination control strategies supporting manufacturing operations and product quality. * Ensure timely delivery of testing results and effective management of deviations, OOS/OOT investigations, CAPAs, change controls, and quality system records. * Maintain oversight of laboratory quality systems, investigations, compliance programs, and data integrity initiatives. * Lead and support analytical method transfers, analytical qualifications, analytical validations, and implementation of analytical changes supporting commercial products and new product introductions. * Provide strategic oversight of analytical method transfer activities across internal and external testing networks. * Review and approve analytical methods, specifications, protocols, reports, stability documentation, and other cGMP records to ensure compliance with internal standards and global regulatory requirements. * Support technology transfers, process transfers, process validation activities, Process Performance Qualification (PPQ) campaigns, and commercial product introductions. * Support regulatory submissions, Annual Product Quality Reviews (APQRs), stability programs, and broader product lifecycle management activities. * Establish and oversee Quality Control performance metrics, data analytics, monitoring programs, and trending systems to support process robustness and product quality. * Partner with Digital and IT organizations to strengthen laboratory systems, automation strategies, data governance capabilities, and digital transformation initiatives across Quality Control operations. * Leverage advanced laboratory technologies, digital platforms, and opportunities to work alongside emerging AI and Generative AI capabilities to improve operational effectiveness, trend analysis, knowledge management, and decision-making. * Lead complex technical investigations and provide scientific expertise to resolve analytical, operational, compliance, and quality-related challenges. * Develop, implement, and maintain laboratory procedures, operational systems, and training programs to ensure sustained cGMP compliance. * Represent Quality Control during regulatory inspections, health authority inspections, customer audits, vendor audits, and internal audits while maintaining a constant state of inspection readiness. * Ensure compliance with global regulatory requirements, GxP regulations, company policies, and internal quality standards. * Execute responsibilities in accordance with internal governing documents including SOPs, work instructions, and quality management system requirements. * Ensure adherence to Good Documentation Practices and Data Integrity requirements, maintaining accurate and inspection-ready records and documentation. * Complete all required training and maintain qualifications in accordance with defined learning plans and requalification requirements. * Contribute to departmental strategy, organizational planning, resource allocation, and budget management to support future business growth. * Build, lead, coach, mentor, and develop a high-performing Quality Control organization. * Manage laboratory personnel including performance management, talent development, employee engagement, succession planning, and career development. * Set clear goals, objectives, and expectations for team members while monitoring performance and execution. * Provide leadership, guidance, and direction to employees aligned with organizational priorities and strategic objectives. * Inspire and motivate team members to achieve their full potential while fostering accountability and ownership. * Establish succession plans and employee development plans to support long-term organizational capability. * Foster a positive, inclusive, collaborative, and innovative culture focused on continuous improvement and operational excellence. * Identify and assign appropriate deputies to ensure business continuity during periods of absence. * Act as an interdepartmental liaison across Analytical Science & Technology, Global Quality Control, External Quality Control, Quality Assurance, Regulatory Affairs, Manufacturing, Engineering, and Supply Chain functions. **The key Moderna Mindsets you’ll need to succeed in the role:** • “We obsess over learning. We don’t have to be the smartest we have to learn the fastest.” • “We digitize everywhere possible using the power of code to maximize our impact on patients.” **Here’s What You’ll Need (Basic Qualifications)** * Bachelor's degree in relevant scientific discipline (Life Sciences, Biotechnology, Chemistry, Microbiology, Biochemistry, or related field); advanced degree preferred. * Minimum of 10 years of experience in Quality Control within a commercial cGMP biotechnology or pharmaceutical environment, including experience supporting both internal and external manufacturing and testing operations. * Minimum of 4–6 years of leadership experience, including management of technical teams, laboratory operations, project management, and talent development. * Strong working knowledge of global regulatory requirements and industry standards, including FDA, Health Canada, EMA, ICH, ISPE, ASTM, and applicable GxP regulations. * Demonstrated experience in analytical testing, method transfer, method qualification, validation, and lifecycle management within the biotechnology or pharmaceutical industry. * Proven expertise in Quality Systems, including Deviations, OOS/OOT investigations, CAPAs, Change Controls, risk assessments, and data integrity programs. * This position is site-based, requiring you to be at Moderna’s site full-time. This position is not eligible for remote work. * As part of Moderna’s commitment to build a sustainable workforce, a minimum of 2 years of work authorization is required for this role. **Here’s What You’ll Bring to the Table (Preferred Qualifications)** * Strong knowledge and experience in Environmental Monitoring, contamination control strategies, and Critical Utilities Monitoring programs within GMP-regulated biotechnology or pharmaceutical manufacturing environments, including regulatory requirements, data analysis, investigations, and inspection readiness. * Experience supporting regulatory inspections, health authority interactions, customer audits, vendor audits, and inspection readiness activities. * Strong knowledge of laboratory operations supporting chemistry, microbiology, bioassay, environmental monitoring, and stability programs. * Experience managing quality control activities at Contract Manufacturing Organizations (CMOs), Contract Testing Laboratories (CTLs), and external partners is highly desirable. * Demonstrated success leading complex analytical projects, investigations, process improvements, and cross-functional initiatives in a fast-paced environment. * Strong technical writing and documentation skills, including review and approval of analytical methods, protocols, reports, specifications, and regulatory documentation. * Proficiency with laboratory and enterprise systems such as LIMS, SAP, LMS, electronic quality management systems, and data analytics tools. * Experience with laboratory instrumentation and software platforms, including chromatographic and analytical technologies, is preferred. * Excellent leadership, interpersonal, communication, and stakeholder management skills, with the ability to influence and collaborate effectively across all organizational levels and external partners. * Demonstrated ability to think strategically, solve complex problems, manage multiple priorities, and navigate ambiguity in a dynamic, matrixed environment. * Strong commitment to operational excellence, continuous improvement, innovation, and fostering a culture of compliance, accountability, and teamwork. * Fluent in English, both written and spoken; additional languages are considered an asset. * A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative. **Rémunération et avantages sociaux** **Chez Moderna, nous croyons que lorsque vous vous sentez au mieux de votre forme, vous pouvez donner le meilleur de vous-même.** C’est pourquoi nos avantages sociaux mondiaux et nos ressources en matière de bien-être sont conçus pour vous soutenir – au travail, à la maison et partout entre les deux. * Des soins de santé de premier ordre, ainsi que des programmes d'avantages volontaires adaptés à vos besoins spécifiques * Une approche holistique du bien-être, avec un accès à des services de remise en forme, de pleine conscience et de soutien en santé mentale * Des avantages pour la construction familiale, y compris un soutien en matière de fertilité, d’adoption et de gestation pour autrui * Des congés généreux, incluant les vacances, les jours fériés, les journées de bénévolat, les congés sabbatiques, les journées mondiales de ressourcement, ainsi qu'une fermeture discrétionnaire en fin d’année * Des solutions d’épargne et d’investissement pour vous aider à planifier votre avenir * Des avantages et extras spécifiques à chaque lieu Les avantages offerts peuvent varier en fonction de la nature de votre emploi chez Moderna et du pays dans lequel vous travaillez **À propos de Moderna** Depuis notre fondation en 2010, nous aspirons à bâtir la principale plateforme technologique d’ARNm, l’infrastructure pour réinventer la manière dont les médicaments sont créés et distribués, ainsi qu’une équipe de calibre mondial. Nous croyons qu’il est important d’offrir à nos employés une plateforme pour transformer la médecine et une opportunité de changer le monde. En vivant notre mission, nos valeurs et nos façons de penser chaque jour, nos employés sont le moteur de notre progrès scientifique et de notre culture. Ensemble, nous créons une culture d’inclusion et bâtissons une organisation qui se soucie profondément de ses patients, de ses employés, de l’environnement et des communautés. Nous sommes fiers d’avoir été reconnus comme un des meilleurs employeurs biopharmaceutiques par _Science Magazine_ , un des meilleurs milieux de travail pour les innovateurs par _Fast Company_ , et un excellent lieu de travail aux États-Unis. En bâtissant notre entreprise, nous avons toujours cru qu’une culture en personne est essentielle à notre succès. Moderna défend les avantages importants de la collaboration en présentiel en adoptant un modèle de travail 70/30. Cette structure — 70 % au bureau — favorise une culture riche en innovation, en travail d’équipe et en mentorat direct. Joignez-vous à nous pour façonner un monde où chaque interaction est une opportunité d’apprendre, de contribuer et d’avoir un impact significatif. Si vous souhaitez faire une différence et rejoindre une équipe qui transforme l’avenir de la médecine, nous vous invitons à visiter [modernatx.com/careers](https://www.modernatx.com/careers) pour en savoir plus sur nos possibilités actuelles. Moderna est un environnement de travail sans fumée, sans alcool et sans drogue. Moderna est un lieu où chacun peut évoluer. Si vous répondez aux qualifications de base du poste et que vous êtes enthousiaste à l’idée de contribuer à notre mission chaque jour, veuillez postuler! Moderna s’engage à offrir l’égalité d’accès à l’emploi et à ne pratiquer aucune discrimination envers ses employés ou les candidats qualifiés, sans égard à la race, à la couleur, au sexe, à l’identité ou l’expression de genre, à l’âge, à la religion, à l’origine nationale, à l’ascendance ou à la citoyenneté, à l’ethnie, à un handicap, au statut militaire ou de vétéran protégé, aux informations génétiques, à l’orientation sexuelle, à l’état civil ou familial, ou à toute autre caractéristique personnelle protégée par la loi en vigueur. Nous étudions les candidatures qualifiées, peu importe les antécédents judiciaires, conformément aux exigences légales. Nous nous concentrons sur l’attraction, la rétention, le développement et la progression de nos employés. En cultivant un milieu de travail qui valorise les expériences, les origines et les idées diversifiées, nous créons un environnement où chaque employé peut donner le meilleur de lui-même. Moderna s’engage à offrir des mesures d’adaptation raisonnables aux candidats qualifiés en situation de handicap. Tout candidat nécessitant une mesure d’adaptation dans le cadre du processus d’embauche et/ou pour exercer les fonctions essentielles du poste pour lequel il postule est invité à contacter l’équipe responsable des congés et des mesures d’adaptation à l’adresse suivante : **leavesandaccommodations @modernatx.com**. \\------------------------------------------------------------------------------------------------------------------------------------------------------ **Pay & Benefits** **At Moderna, we believe that when you feel your best, you can do your best work. That’s why our global benefits and well-being resources are designed to support you—at work, at home, and everywhere in between.** * Best-in-class healthcare, plus voluntary benefit programs to support your unique needs * A holistic approach to well-being with access to fitness, mindfulness, and mental health support * Family building benefits, including fertility, adoption, and surrogacy support * Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown * Savings and investments to help you plan for the future * Location-specific perks and extras The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work. **About Moderna** Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world. By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities. We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit [modernatx.com/careers](https://www.modernatx.com/en-US/careers/life-at-moderna) to learn more about our current opportunities. Moderna is a smoke-free, alcohol-free, and drug-free work environment. Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply! Moderna is committed to equal opportunity in employment and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. We’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best. Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at [leavesandaccommodations@modernatx.com](mailto:leavesandaccommodations@modernatx.com%22%20\\\\o%20%22mailto:leavesandaccommodations@modernatx.com%22%20\\\\t%20%22_blank). -", "summaryDescription" : "Associate Director, Quality Control at Moderna", "postedDate" : "2026-06-16T03:45:12.619", "createdAt" : "2026-06-16T03:45:12.607", "lastUpdated" : "2026-06-16T13:07:21.885", "ingestTimestamp" : "2026-06-16T03:45:12.607", "mongoId" : "6a305611f292fd229cf24978", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://modernatx.wd1.myworkdayjobs.com/M_tx/job/Laval---Canada/Associate-Director--Quality-Control_R19304", "salaryBand" : "150k-200k", "hasSalary" : false, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "executive", "dataQualityScore" : 0.8888889, "_score" : 787.51587, "daysOld" : 0, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c7f0074d8ee00a0954465", "title" : "Senior Quality Assurance Engineer", "company" : "iFIT", "industry" : "Manufacturing", "salary" : { "min" : 75000.0, "max" : 85000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Logan, Utah, United States", "locations" : [ "Logan", "Utah", "United States" ], "certifications" : [ "ASQ Certified Quality Engineer (CQE)", "Six Sigma Greenlack Belt certification" ], "timestamp" : "2026-06-15T08:10:23.821", "fingerprint" : "eae2ffa0a89d93d755e3cad20eab0493144808d36fe17a81965dacdcc22a5510", "source" : "greenhouse", "language" : "en", "applyUrl" : "http://www.ifit.com/careers?gh_jid=4257201009", "externalId" : "4257201009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Logan", "state" : "Utah", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "41.7313063,-111.8349140" } ], "locationText" : "Logan, Utah, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "FMEA, SPC, Weibull Analysis, Fault Tree Analysis, Six Sigma", "professionalSkills" : [ "Root cause analysis", "Corrective actions", "Process capability", "Quality management", "Supplier accountability" ], "hardSkillsList" : [ "Quality engineering", "Warranty analysis", "CAPA management" ], "softSkillsList" : [ "Critical thinking" ], "hardSkills" : [ { "name" : "Quality engineering", "level" : "intermediate" }, { "name" : "Warranty analysis", "level" : "intermediate" }, { "name" : "CAPA management", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Critical thinking" } ], "majorSkills" : "Quality Assurance, Root Cause Analysis, Supplier Quality", "majorSkillsList" : [ "Quality Assurance", "Root Cause Analysis", "Supplier Quality" ], "coreResponsibilities" : "Drive reduction of Cost of Poor Quality, Analyze customer complaints, Analyze warranty data, Analyze out-of-box experience trends, Lead corrective actions, Facilitate Root Cause Analysis, Own each case to closure, Operationalize QMS policies, Operationalize procedures, Operationalize work instructions, Support audits, Support customer visits, Support factory acceptance tests, Partner with Design Engineering, Partner with Manufacturing Engineering, Define process parameters, Validate supplier process capability, Prepare quality performance reports, Provide recurring training, Communicate with foreign vendors", "teamCollaboration" : "Cross-functional collaboration; Work with suppliers; Partner with Engineering", "projectManagementSkills" : [ "8D methodology" ], "domainKnowledge" : "Health and fitness platform; Customer quality; Supply base management; Field failures; Warranty data; Out-of-box experience; Cost of Poor Quality; Perfect Order Index; Supplier CAPA; QMS policies; Product requirements; Overseas contract manufacturers", "domainList" : [ "health-and-fitness-platform", "customer-quality", "supply-base-management", "field-failures", "warranty-data", "out-of-box-experience", "cost-of-poor-quality", "perfect-order-index", "supplier-capa", "qms-policies", "product-requirements", "overseas-contract-manufacturers" ], "domainSpecificKnowledge" : [ "Health and fitness platform", "Customer quality", "Supply base management", "Field failures", "Warranty data", "Out-of-box experience", "Cost of Poor Quality", "Perfect Order Index", "Supplier CAPA", "QMS policies", "Product requirements", "Overseas contract manufacturers" ], "communicationSkills" : "Communicate with foreign vendors", "documentationSkills" : "Prepare quality performance reports", "innovationCreativity" : "Champion AI adoption; Implement AI initiative", "problemSolvingSkills" : "Root Cause Analysis; Critical thinking", "specialRequirements" : "Communicate after hours", "outcomesObjectives" : "Improve customer experience; Drive measurable improvement in Perfect Order Index; Achieve Cost of Poor Quality warranty targets; Reduce Cost of Poor Quality; Trace recurring customer complaint to root cause; Close supplier CAPA effectively; Trend Cost of Poor Quality down", "qualificationsBasic" : "Hands-on experience with SPC, Hands-on experience with DFMEA/PFMEA, Hands-on experience with Weibull Analysis, Hands-on experience with Fault Tree Analysis, Hands-on experience with Six Sigma methodology, Experience working with overseas contract manufacturers, Familiarity with ISO 9001 QMS rollouts, Familiarity with audit support", "qualificationsPreferred" : "3Dconnexion SpacePilot experience a plus, ASQ Certified Quality Engineer (CQE), Six Sigma Greenlack Belt certification", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "iFIT’s vision is to create the world's most holistic health and fitness platform, integrating all elements of health - physical fitness, mental health, nutrition and active recovery - into a seamless interactive experience. We develop proprietary software that learns and adjusts to the habits of each person as it delivers immersive content that guides them on their own individual fitness journey. We are currently seeking an ambitious pace-setter to join our team as a Customer Quality Engineer onsite in Logan, Utah. iFIT is looking for a detail-oriented and driven Customer Quality Engineer to serve as the closed-loop owner between iFIT customers and our supply base. In this role, you will translate field failures, warranty data, and out-of-box experience issues into root cause investigations and corrective actions with suppliers and internal engineering. A great day means a recurring customer complaint gets traced to a true root cause, a supplier CAPA closes effectively, and Cost of Poor Quality trends down on the next report. COMPENSATION $75,000 - $85,000 ROLE COMMITMENTS Improve the customer experience by driving measurable improvement in the Perfect Order Index through targeted quality initiatives and cross-functional collaboration. Sustain earnings by achieving Cost of Poor Quality warranty targets through proactive quality management and supplier accountability. Champion AI adoption by implementing at least one AI initiative focused on replacing repetitive or highly manual quality tasks to improve team efficiency and employee experience. Increase profitability by reducing Cost of Poor Quality through QPA investigations and continuous quality improvement activities. ESSENTIAL DUTIES AND RESPONSIBILITIES Drive reduction of Cost of Poor Quality (COPQ) by analyzing customer complaints, warranty data, and out-of-box experience trends, then leading corrective actions back through engineering and suppliers. Facilitate Root Cause Analysis using 8D, 5-Why, and FMEA methodologies on supplier and product quality issues, owning each case to verified, effective closure. Operationalize QMS policies, procedures, and work instructions on the production floor, and support audits, customer visits, and factory acceptance tests. Partner with Design and Manufacturing Engineering to define process parameters and validate supplier process capability against product requirements. Prepare quality performance reports and recurring training for the Quality team, and communicate with foreign vendors after hours as needed. EDUCATION 3Dconnexion SpacePilot experience a plus. Hands-on experience with SPC, DFMEA/PFMEA, Weibull Analysis, Fault Tree Analysis, and Six Sigma methodology. ASQ Certified Quality Engineer (CQE) or Six Sigma Green/Black Belt certification. Experience working with overseas contract manufacturers in China, Taiwan, or Vietnam. Familiarity with ISO 9001 QMS rollouts and audit support. Comfortable in a fast-paced environment with strong critical thinking skills and the ability to inspire the same in others. DISCLAIMER Compensation may vary based on the job level, your geographic work location, position incentive plan, and exemption status. Although we currently may consider hiring in the states listed below, not all positions are available in all locations, and work in a particular state is not guaranteed. Current list of states where iFIT may consider hiring: AK, AL, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WY. Subject to applicable state laws, your employment at iFIT is \"at-will\". At-will employment means that you and the company each have the right to terminate the employment relationship at any time for any cause or for no cause at all. Pay Range: $75,000—$85,000 USD iFIT does not discriminate in employment opportunities or practices on the basis of race, color, religion, sex, national origin, age, ancestry, mental or physical disability, sexual orientation, gender identity, medical condition, genetic information, marital status, veteran status or any other characteristic protected by law.", "summaryDescription" : "Senior Quality Assurance Engineer at iFIT. Skills: Quality Assurance, Root Cause Analysis, Supplier Quality. Drive reduction of Cost of Poor Quality. Analyze customer complaints", "postedDate" : "2026-06-14T05:38:03.364", "createdAt" : "2026-06-14T05:38:03.364", "lastUpdated" : "2026-06-15T08:10:23.821", "ingestTimestamp" : "2026-06-14T05:38:03.364", "mongoId" : "6a2c7f0074d8ee00a0954465", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 75000, "salaryAnnualMax" : 85000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Quality engineering", "Warranty analysis", "CAPA management", "Critical thinking", "Quality Assurance", "Root Cause Analysis", "Supplier Quality", "Root cause analysis", "Corrective actions", "Process capability", "Quality management", "Supplier accountability", "8D methodology", "Health and fitness platform", "Customer quality", "Supply base management", "Field failures", "Warranty data", "Out-of-box experience", "Cost of Poor Quality", "Perfect Order Index", "Supplier CAPA", "QMS policies", "Product requirements", "Overseas contract manufacturers", "ASQ Certified Quality Engineer (CQE)", "Six Sigma Greenlack Belt certification" ], "skillCount" : 27, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 1.0, "_score" : 784.5527, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.95 }, { "id" : "6a30564af292fd229cf26e39", "title" : "Quality Assurance Engineer", "company" : "ADCI", "industry" : "Systems, Quality, Security Engineering, Systems Quality, alexa and amazon devices", "salary" : { "min" : 1200000.0, "max" : 2000000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Quality Assurance Engineer in Bengaluru, India, with adjustments for the technology industry and company size." }, "location" : "Bengaluru, Karnataka, IND", "locations" : [ "Bengaluru, Karnataka, IND" ], "timestamp" : "2026-06-16T07:12:37.557", "fingerprint" : "4b35c6ca28ffe06b3a4098fbde41b11632805e5395c99a7a405fe7a967aa7fa9", "source" : "amazon", "language" : "en", "applyUrl" : "https://account.amazon.jobs/jobs/10449091/apply", "externalId" : "91e1c3c1-52f2-4b97-888c-4a13e4be1464", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Bengaluru", "state" : "Karnataka", "country" : "India", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "12.9767936,77.5900820" } ], "locationText" : "Bengaluru, Karnataka, India", "employmentType" : "FULL_TIME", "experienceMinYears" : 4, "experienceMaxYears" : 5, "experienceLevel" : "Mid", "technicalSkills" : "Android, IOS, Selenium, Appium", "hardSkillsList" : [ "Test automation", "Scripting", "Coding" ], "hardSkills" : [ { "name" : "Test automation", "level" : "intermediate" }, { "name" : "Scripting", "level" : "intermediate" }, { "name" : "Coding", "level" : "intermediate" } ], "majorSkills" : "Quality Assurance, Test automation, Test strategy", "majorSkillsList" : [ "Quality Assurance", "Test automation", "Test strategy" ], "coreResponsibilities" : "Develop test strategies, Develop test plans, Develop automated test cases, Build test infrastructure, Build test environment, Support manual test execution, Support automation test execution, Create test plans, Execute test plans, Maintain test plans, Create automation scripts, Maintain automation scripts, Execute automated test cases, Debug test failures, Troubleshoot automation failures, Isolate bugs, Perform initial defect triage, Perform root cause analysis, Escalate roadblocks, Escalate risks, Improve test mechanisms, Improve best practices", "domainKnowledge" : "Emerging devices; Consumer electronics; Mobile applications", "domainList" : [ "emerging-devices", "consumer-electronics", "mobile-applications" ], "domainSpecificKnowledge" : [ "Emerging devices", "Consumer electronics", "Mobile applications" ], "toolProficiency" : [ "Selenium", "Appium" ], "documentationSkills" : "Test plans; Test designs", "problemSolvingSkills" : "Troubleshooting products; Root cause analysis", "qualificationsBasic" : "4+ years of quality assurance engineering experience, Experience in manual testing, Experience in automation testing, Experience scripting or coding, Experience developing high quality test plans, Experience developing test designs, Experience developing test strategies, Experience developing test execution", "qualificationsPreferred" : "Experience with Android, Experience with iOS, Experience with other mobile application development, Experience with other mobile application testing, Experience with at least one automated test framework, Experience with embedded systems, Experience with consumer devices, Experience with mobile apps", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Do you enjoy solving complex problems and troubleshooting products? Are you passionate about developing test strategies, finding and tracking bugs to resolution, and innovating on behalf of customers? Do you want to be a part of a fast-paced, ambiguous environment and contribute to the creation of next generation products? We are looking for an experienced, self-motivated, and detail-oriented QA engineer with a proven ability to deliver results in a fast-paced, complex hardware and software environment. The challenges Quality Assurance Engineers solve at Amazon are big and impact millions of customers, and products around the world. Our path is not always simple, so we are selective about who joins us on this journey. There is a certain kind of person who takes on this role at Amazon – someone who is excited by the idea of creating new products, features, and services from scratch while managing ambiguity and the rapid pace of our company Come chart your own path at Amazon. Key job responsibilities - Develop test strategies, test plans, and automated test cases - Build test infrastructure/environment to support manual and automation test execution - Use technical knowledge to create, execute, and maintain test plans and automation involving one or more product components and/or features - Create and maintain automation scripts, and execute automated test cases. - Debug/Troubleshoot test failures/automation failures and isolate bugs to help developers research the root cause of defects - Perform initial defect triage and root cause analysis, and escalate roadblocks/risks - Improve test mechanisms and best practices About the team The Amazon Emerging Devices Software (EDS) is part of the Amazon Devices team. We design and engineer high-profile consumer electronics, including the best-selling Echo devices. Our portfolio also includes innovative devices like Amazon Echo buds, Echo Frames and Echo Auto. What will you help us create next? Basic Qualifications: - 4+ years of quality assurance engineering experience - Experience in manual testing - Experience in automation testing - Experience scripting or coding - Experience developing high quality test plans, test designs, test strategies, and test execution Preferred Qualifications: - Experience with Android, iOS or other mobile application development or testing - Experience with at least one automated test framework like Selenium or Appium - Experience with embedded systems, consumer devices, or mobile apps Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit https://amazon.jobs/content/en/how-we-hire/accommodations for more information. If the country/region you’re applying in isn’t listed, please contact your Recruiting Partner.", "summaryDescription" : "Quality Assurance Engineer at ADCI. Skills: Quality Assurance, Test automation, Test strategy. Develop test strategies. Develop test plans", "postedDate" : "2026-06-15T00:00:00.000", "createdAt" : "2026-06-15T21:58:00.429", "lastUpdated" : "2026-06-16T07:12:37.557", "ingestTimestamp" : "2026-06-15T21:58:00.429", "mongoId" : "6a30564af292fd229cf26e39", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.jobs/jobs/10449091/apply", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Test automation", "Scripting", "Coding", "Quality Assurance", "Test strategy", "Emerging devices", "Consumer electronics", "Mobile applications", "Selenium", "Appium" ], "skillCount" : 10, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 1.0, "_score" : 778.9387, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.98 }, { "id" : "6a305d2bf292fd229cf64e93", "title" : "Sr. Manager, GMP Quality Assurance", "company" : "Deciphera Pharmaceuticals", "industry" : "Pharmaceuticals", "salary" : { "min" : 138000.0, "max" : 190000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Waltham, MA, United States", "locations" : [ "Waltham", "MA", "United States" ], "timestamp" : "2026-06-16T09:20:54.784", "fingerprint" : "482ae4204da4bec29094febdf4fd99c63214d1db7bf6039af1e17a7fa9274ae3", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/DecipheraPharmaceuticals1/744000132169080-sr-manager-gmp-quality-assurance", "externalId" : "744000132169080", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Waltham", "state" : "Massachusetts", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "42.3762385,-71.2355644" } ], "locationText" : "Waltham, Massachusetts, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "professionalSkills" : [ "Quality Systems", "Batch Release", "GMP Oversight", "Regulatory Compliance", "Investigations", "Deviations", "CAPA", "Change Controls", "Audits", "Inspections", "Product Reviews", "Quality Improvements", "Quality Metrics", "CMO Partnership", "Supplier Partnership", "Validation", "Tech Transfer", "Qualification", "Staff Mentoring", "Staff Development" ], "softSkillsList" : [ "Leadership" ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "GMP Quality Assurance, Quality Systems, Regulatory Compliance", "majorSkillsList" : [ "GMP Quality Assurance", "Quality Systems", "Regulatory Compliance" ], "coreResponsibilities" : "Lead batch release activities, Review/approve batch records, Review/approve material disposition, Provide GMP oversight for manufacturing partners, Provide GMP oversight for distribution partners, Ensure compliance with global regulations, Manage investigations, Manage deviations, Manage CAPA, Manage change controls, Support audits, Support inspections, Support annual product reviews, Drive quality system improvements, Track key quality metrics, Partner with CMOs, Partner with suppliers, Mentor junior QA staff, Develop junior QA staff", "teamCollaboration" : "Internal teams; External partners; CMOs; Suppliers", "domainKnowledge" : "GMP; GDP regulations; FDA; EMA; ICH; Life sciences; Chemistry", "domainList" : [ "gmp", "gdp-regulations", "fda", "ema", "ich", "life-sciences", "chemistry" ], "domainSpecificKnowledge" : [ "GMP", "GDP regulations", "FDA", "EMA", "ICH", "Life sciences", "Chemistry" ], "toolProficiency" : [ "Veeva" ], "communicationSkills" : "Stakeholder management", "continuousLearning" : "Professional growth opportunities", "problemSolvingSkills" : "Solve complex problems", "specialRequirements" : "Up to 20% travel", "qualificationsBasic" : "Bachelor's degree in life sciences, 8+ years GMP Quality experience, Knowledge of global GMP regulations, Knowledge of quality systems, Ability to lead cross-functional initiatives, Ability to solve complex problems, Excellent communication skills, Excellent stakeholder management skills, Authorized to work in the U.S", "qualificationsPreferred" : "Experience with eQMS, Experience with global markets", "remoteFriendly" : true, "workSiteFlexibility" : "Flexible", "rawDescription" : "We are seeking a Senior Manager, GMP Quality Assurance to support and continuously improve Quality Systems across clinical and commercial products. This role provides leadership across internal teams and external partners to ensure compliance with global GMP/GDP regulations and company standards. Key Responsibilities * Lead batch release activities, including review/approval of batch records and material disposition * Provide GMP oversight for manufacturing and distribution partners (DS, DP, and supply chain) * Ensure compliance with global regulations (FDA, EMA, ICH) * Manage investigations, deviations, CAPA, and change controls * Support audits, inspections, and annual product reviews * Drive quality system improvements and track key quality metrics * Partner with CMOs and suppliers on validation, tech transfer, and qualification activities * Mentor and develop junior QA staff ## Qualifications Qualifications * Bachelor’s degree in life sciences, chemistry, or related field * 8+ years of GMP Quality experience in pharma or biotech * Strong knowledge of global GMP regulations and quality systems * Proven ability to lead cross-functional initiatives and solve complex problems * Excellent communication and stakeholder management skills Additional Details * Experience with eQMS (e.g., Veeva) and global markets is a plus * Up to 20% travel may be required * Must be authorized to work in the U.S. ## Additional Information Deciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $138,000 - $190,000. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location. Deciphera believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Deciphera’s competitive total rewards strategy that also includes annual performance bonus, a long-term incentive plan, full range of benefits and other incentive compensation plans (if applicable) Benefits: * Competitive salary and annual bonus. * Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match, and more. * Generous parental leave and family planning benefits. * Outstanding culture and opportunities for personal and professional growth. EQUAL EMPLOYMENT OPPORTUNITY INFORMATION Deciphera is committed to equal employment opportunity and values diversity. To ensure that we comply with reporting requirements, we invite you complete the confidential survey at the end of this application. Providing this information is optional. It will not be accessible or used in the hiring process, and has no effect on your opportunity for employment. This information will also be treated confidentially. We are committed to make all hiring decisions and other employment decisions on a non-discriminatory basis.", "summaryDescription" : "Sr. Manager, GMP Quality Assurance at Deciphera Pharmaceuticals. Skills: GMP Quality Assurance, Quality Systems, Regulatory Compliance. Lead batch release activities. Review/approve batch records", "postedDate" : "2026-06-15T10:58:10.000", "createdAt" : "2026-06-15T23:58:50.457", "lastUpdated" : "2026-06-16T09:20:54.784", "ingestTimestamp" : "2026-06-15T23:58:50.457", "mongoId" : "6a305d2bf292fd229cf64e93", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 138000, "salaryAnnualMax" : 190000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Leadership", "GMP Quality Assurance", "Quality Systems", "Regulatory Compliance", "Batch Release", "GMP Oversight", "Investigations", "Deviations", "CAPA", "Change Controls", "Audits", "Inspections", "Product Reviews", "Quality Improvements", "Quality Metrics", "CMO Partnership", "Supplier Partnership", "Validation", "Tech Transfer", "Qualification", "Staff Mentoring", "Staff Development", "GMP", "GDP regulations", "FDA", "EMA", "ICH", "Life sciences", "Chemistry", "Veeva" ], "skillCount" : 30, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Manager", "dataQualityScore" : 1.0, "_score" : 768.6451, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "69e111412beec4dd3df29f89", "title" : "Supply Chain Director", "company" : "Gotion, Inc.", "location" : "Manteno, Illinois, United States", "locations" : [ "Manteno", "Illinois", "United States" ], "certifications" : [ ], "timestamp" : "2026-06-15T07:01:18.896", "fingerprint" : "d8713d53cea23e47e677bf294055774cf05b2e0af9fb7fddab2c4b897b226da6", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/gotion/jobs/8395020002", "externalId" : "8395020002", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Manteno", "state" : "Illinois", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite" } ], "locationText" : "Manteno, Illinois, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor", "experienceMinYears" : 10, "experienceMaxYears" : 15, "experienceLevel" : "Director", "technicalSkills" : "ERP/MRP systems", "professionalSkills" : [ "EV battery manufacturing experience is a plus." ], "hardSkillsList" : [ "supply chain leadership", "global supply chains", "sourcing strategy", "logistics", "inventory management", "lean manufacturing", "Six Sigma" ], "softSkillsList" : [ "leadership, team development, problem-solving, communication, collaboration" ], "hardSkills" : [ { "name" : "supply chain leadership", "level" : "intermediate" }, { "name" : "global supply chains", "level" : "intermediate" }, { "name" : "sourcing strategy", "level" : "intermediate" }, { "name" : "logistics", "level" : "intermediate" }, { "name" : "inventory management", "level" : "intermediate" }, { "name" : "lean manufacturing", "level" : "intermediate" }, { "name" : "Six Sigma", "level" : "intermediate" } ], "softSkills" : [ { "name" : "leadership, team development, problem-solving, communication, collaboration" } ], "majorSkills" : "Supply Chain Director, high-volume manufacturing, global supply chains, sourcing strategy, inventory management", "majorSkillsList" : [ "Supply Chain Director, high-volume manufacturing, global supply chains, sourcing strategy, inventory management" ], "coreResponsibilities" : "Manage global supply chains, sourcing strategy, logistics, and inventory management.", "teamCollaboration" : "Excellent collaboration skills.", "toolProficiency" : [ "supply chain analytics" ], "communicationSkills" : "communication; collaboration", "problemSolvingSkills" : "problem-solving; continuous improvement methodologies", "specialRequirements" : "Willingness to be based in Manteno, IL, with occasional travel.", "outcomesObjectives" : "This provides you with the opportunity to progress as you grow and advance your career at Gotion.", "qualificationsBasic" : "10–15 years of progressive supply chain leadership experience, preferably in high-volume manufacturing or EV/automotive industries. Experience managing global supply chains, sourcing strategy, logistics, and inventory management. Proficient with ERP/MRP systems and supply chain analytics. leadership, team development, and problem-solving skills. Experience with lean manufacturing, Six Sigma, or continuous improvement methodologies. Excellent communication and collaboration skills. Willingness to be based in Manteno, IL, with occasional travel.", "qualificationsPreferred" : "MBA preferred. EV battery manufacturing experience is a plus.", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Gotion Inc. is based in Silicon Valley, CA, currently building a Manufacturing facility in Manteno, IL and has R MBA preferred. 10–15 years of progressive supply chain leadership experience, preferably in high-volume manufacturing or EV/automotive industries. Experience managing global supply chains, sourcing strategy, logistics, and inventory management. Proficient with ERP/MRP systems and supply chain analytics. Strong leadership, team development, and problem-solving skills. Experience with lean manufacturing, Six Sigma, or continuous improvement methodologies. Excellent communication and collaboration skills. Willingness to be based in Manteno, IL, with occasional travel. EV battery manufacturing experience is a plus. Base pay is one part of our total compensation package at Gotion, and is determined within a range. This provides you with the opportunity to progress as you grow and advance your career at Gotion. The base pay range for this role is shown below, and will depend on your skills, qualifications, experiences, and location. Expected Pay Range $180,000—$230,000 USD Gotion Inc. is proud to be an equal opportunity employer. We are dedicated to fostering a diverse workforce that reflects the communities we serve, cultivating a culture of inclusion and belonging, and ensuring equal employment opportunities for all. We provide equal opportunity to all individuals regardless of race, creed, color, religion, gender, sexual orientation, gender identity or expression, national origin, disability, age, genetic information, veteran status, marital status, pregnancy or related conditions (including breastfeeding), parental status, criminal histories consistent with legal requirements, or any other characteristic protected by law. At Gotion Inc., we strive to create an environment where everyone feels valued, respected, and empowered to thrive.", "summaryDescription" : "Supply Chain Director at Gotion, Inc.. Skills: Supply Chain Director, high-volume manufacturing, global supply chains, sourcing strategy, inventory management. Manage global supply chains, sourcing strategy, logistics, and inventory management.", "postedDate" : "2026-06-14T20:53:29.428", "createdAt" : "2026-06-14T20:53:29.428", "lastUpdated" : "2026-06-15T07:01:18.896", "ingestTimestamp" : "2026-06-14T20:53:29.428", "mongoId" : "69e111412beec4dd3df29f89", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "hasSalary" : false, "allSkills" : [ "supply chain leadership", "global supply chains", "sourcing strategy", "logistics", "inventory management", "lean manufacturing", "Six Sigma", "leadership, team development, problem-solving, communication, collaboration", "Supply Chain Director, high-volume manufacturing, global supply chains, sourcing strategy, inventory management", "EV battery manufacturing experience is a plus.", "supply chain analytics" ], "skillCount" : 11, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 760.0664, "daysOld" : 0, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Manufacturing", "llmIndustryConfidence" : 0.98 }, { "id" : "6a3065a0f292fd229cfa9f3c", "title" : "Senior Director, Sales", "company" : "Venn", "industry" : "Sales", "salary" : { "min" : 225000.0, "max" : 325000.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Director, Sales in Toronto, Canada, adjusted for the FinTech industry and full-time employment." }, "location" : "Toronto", "locations" : [ "Toronto" ], "timestamp" : "2026-06-16T13:28:14.385", "fingerprint" : "a9d36d71b523cf78eb99ae393810d9c0f9b704b2748ed0277ffba6b884926f72", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/venn/6d2a0c48-0bbc-4a5f-a7c3-5b8aeb32381a/application", "externalId" : "6d2a0c48-0bbc-4a5f-a7c3-5b8aeb32381a", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Toronto", "state" : "Ontario", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "43.6534817,-79.3839347" } ], "locationText" : "Toronto, Ontario, Canada", "employmentType" : "FULL_TIME", "experienceMinYears" : 7, "experienceLevel" : "Director", "technicalSkills" : "AI", "professionalSkills" : [ "Sales enablement", "GTM strategy", "Territory design", "Pipeline management", "Forecasting", "Deal review", "Coaching" ], "hardSkillsList" : [ "Quota attainment", "Sales coaching", "Sales enablement", "Forecasting", "Pipeline management", "Territory design", "ICP targeting", "GTM strategy" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Quota attainment", "level" : "intermediate" }, { "name" : "Sales coaching", "level" : "intermediate" }, { "name" : "Sales enablement", "level" : "intermediate" }, { "name" : "Forecasting", "level" : "intermediate" }, { "name" : "Pipeline management", "level" : "intermediate" }, { "name" : "Territory design", "level" : "intermediate" }, { "name" : "ICP targeting", "level" : "intermediate" }, { "name" : "GTM strategy", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "Sales leadership, Revenue generation, Team management, GTM strategy", "majorSkillsList" : [ "Sales leadership", "Revenue generation", "Team management", "GTM strategy" ], "coreResponsibilities" : "Lead sales team, Manage sales team, Scale sales team, Set goals for team, Run 1:1s with team, Coach team to quota, Hold team accountable for performance, Own sales enablement end-to-end, Manage onboarding, Manage ramping, Manage ongoing training, Develop playbooks, Manage sales tooling, Run weekly deal review, Pressure-test forecast pipeline, Unblock late-stage deals, Build GTM engine for BDRs, Design BDR sequencing, Design BDR cadences, Design territory, Target ICP, Establish feedback loops, Partner on GTM strategy, Partner on pricing experiments, Partner on metrics, Work cross-functionally with Marketing, Work cross-functionally with Product, Work cross-functionally with Ops, Shape roadmap with sales feedback, Shape demand engine with sales feedback", "teamCollaboration" : "Cross-functional with Marketing; Cross-functional with Product; Cross-functional with Ops", "domainKnowledge" : "B2B sales; Fintech; Business banking; Digital banking; SMB financial services; Horizontal SaaS", "domainList" : [ "b2b-sales", "fintech", "business-banking", "digital-banking", "smb-financial-services", "horizontal-saas" ], "domainSpecificKnowledge" : [ "B2B sales", "Fintech", "Business banking", "Digital banking", "SMB financial services", "Horizontal SaaS" ], "qualificationsBasic" : "7+ years in B2B sales, 2+ years leading BDRs, 2+ years leading AEs, Track record of hitting quota, Ability to define GTM strategy, Ability to build scalable motions, Sales operating rhythm, Forecasting discipline, Deal review, Pipeline hygiene, Leverage AI to improve sales productivity, Leverage AI for pipeline generation, Leverage AI for customer engagement, Incorporate AI tools into prospecting, Incorporate AI tools into research, Incorporate AI tools into personalization, Incorporate AI tools into deal strategy", "qualificationsPreferred" : "Experience at early-stage startup, Experience at fast-growing startup, Experience selling B2B fintech, Experience selling SMB financial services, Experience selling horizontal SaaS, Built outbound BDR function from <5 to 10+", "remoteFriendly" : true, "rawDescription" : "ABOUT VENN Venn is the fastest-growing B2B fintech in Canada. We're on a mission to transform business banking for Canadian entrepreneurs and are looking to hire A-players interested in disrupting traditional banking practices. As the ONLY digital banking platform in Canada offering a truly modern solution, we have seen accelerated growth—scaling to support more than 10,000 Canadian businesses in under two years. Business owners are tired of the big banks' monopoly and are looking for modern tools that replace the legacy systems that have been their only option for over 100 years. We've raised over $26.5M from Tier 1 investors such as Gradient, Left Lane Capital, Intact, and XYZ Venture Capital. Interested in redefining the future of banking in Canada? Look no further. ABOUT THE ROLE This is a high-impact leadership role stepping in to lead our sales organization - you’ll continue to build the sales engine, sharpen the fundamentals, and set the team up to compound. You'll report directly to the co-founders and own the day-to-day of how Venn sells. WHAT YOU'LL BE DOING - Lead, manage and scale a team of Account Executives and BDRs—setting goals, running 1:1s, coaching to quota, and holding the bar on performance. - Own sales enablement end-to-end: onboarding, ramping, ongoing training, playbooks, and the tooling that makes the team faster. - Run weekly deal review and forecast calls; pressure-test pipeline, unblock late-stage deals, and make sure nothing slips through the cracks. - Build the GTM engine for BDRs—sequencing, cadences, territory design, ICP targeting, and the feedback loops between outbound activity and pipeline quality. - Partner with the team on overall GTM strategy, pricing experiments, and the metrics that matter (pipeline coverage, conversion rates, ramp time, win rate, ACV). - Work cross-functionally with Marketing, Product, and Ops to make sure sales feedback shapes the roadmap and the demand engine. WHAT YOU'LL NEED - 7+ years in B2B sales, with 2+ years leading and managing BDRs and/or AEs in a high-growth environment. - A track record of hitting (and helping a team hit) quota in a fast-paced startup or scale up. - Proven ability to define and execute GTM strategy while building scalable, repeatable motions across segments. - Strong sales operating rhythm: forecasting discipline, deal review, pipeline hygiene, and a clear point of view on what great looks like. - Coaching instinct. You can listen to a call, watch a demo, or read a deal note and tell someone exactly what to do differently tomorrow. - Demonstrated ability to leverage AI to improve sales productivity, pipeline generation, and customer engagement. - Experience incorporating AI tools and workflows into prospecting, research, personalization, and deal strategy. BONUS POINTS - Experience at an early-stage or fast-growing startup - Experience selling B2B fintech, SMB financial services, or horizontal SaaS - Built or scaled an outbound BDR function from <5 to 10+ PERKS & BENEFITS - Healthy equity ownership, among the most generous in the market, aligning your success with the company's growth. - Comprehensive coverage of medical, dental, and vision insurance. - Opportunity to shape the future of business banking in Canada and beyond.", "summaryDescription" : "Senior Director, Sales at Venn. Skills: Sales leadership, Revenue generation, Team management, GTM strategy. Lead sales team. Manage sales team", "createdAt" : "2026-06-16T00:31:16.218", "lastUpdated" : "2026-06-16T13:28:14.385", "ingestTimestamp" : "2026-06-16T00:31:16.218", "mongoId" : "6a3065a0f292fd229cfa9f3c", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Quota attainment", "Sales coaching", "Sales enablement", "Forecasting", "Pipeline management", "Territory design", "ICP targeting", "GTM strategy", "Leadership", "Sales leadership", "Revenue generation", "Team management", "Deal review", "Coaching", "B2B sales", "Fintech", "Business banking", "Digital banking", "SMB financial services", "Horizontal SaaS" ], "skillCount" : 20, "jobCategory" : "sales", "jobSubcategory" : "revenue", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 750.9422, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "FinTech", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2ac53174d8ee00a0700b87", "title" : "Senior Director, Product Quality Assurance", "company" : "Beam Therapeutics", "industry" : "Biotechnology", "salary" : { "min" : 260000.0, "max" : 320000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Cambridge, Massachusetts, United States", "locations" : [ "Cambridge", "Massachusetts", "United States" ], "timestamp" : "2026-06-14T20:41:25.136", "fingerprint" : "4f90894b9f408e40814f375adbedeb65ffb3752617002e746df3e7b51cf3d006", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/beamtherapeutics/jobs/8583935002", "externalId" : "8583935002", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Cambridge", "state" : "Massachusetts", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "42.3656347,-71.1040018" } ], "locationText" : "Cambridge, Massachusetts, United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "professionalSkills" : [ "Quality assurance", "GMP compliance", "CDMO management", "Quality systems", "Risk analysis", "Product release", "Regulatory filings", "GxP Auditing", "Quality oversight" ], "hardSkillsList" : [ "Drug substance manufacture", "Drug product manufacture", "Method validation", "Instrument qualification", "Batch record review", "Audit preparation" ], "softSkillsList" : [ "Leadership", "Critical thinking" ], "hardSkills" : [ { "name" : "Drug substance manufacture", "level" : "intermediate" }, { "name" : "Drug product manufacture", "level" : "intermediate" }, { "name" : "Method validation", "level" : "intermediate" }, { "name" : "Instrument qualification", "level" : "intermediate" }, { "name" : "Batch record review", "level" : "intermediate" }, { "name" : "Audit preparation", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Critical thinking" } ], "majorSkills" : "Product Quality Assurance, GMP Compliance, CDMO Oversight", "majorSkillsList" : [ "Product Quality Assurance", "GMP Compliance", "CDMO Oversight" ], "coreResponsibilities" : "Create compliance levels in CDMOs, Monitor compliance levels in CDMOs, Maintain compliance levels in CDMOs, Ensure GMP compliance for external manufacturing, Provide guidance on internal GMP activities, Support Quality for GMP operations, Oversee external GMP operations, Provide QC support in Cambridge, Manage CDMOs/external partners from quality perspective, Work cross-functionally with CMC, Vet CDMOs/external partners, Establish KPI and metrics program, Govern CDMO relationships, Improve CDMO oversight processes, Define Quality objectives, Ensure progress of objectives, Drive risk analysis, Drive risk mitigation strategies, Implement quality systems for product release, Monitor performance to targets, Implement systems for investigation follow up, Implement systems for audit observation closure, Analyze exceptions for CAPA, Analyze exceptions for product impact, Provide technical expertise for quality decisions, Evaluate facility for compliance, Evaluate procedures for compliance, Evaluate equipment for compliance, Evaluate personnel for compliance, Evaluate processes for compliance, Oversee external product manufacture quality, Oversee QC activities quality, Ensure hands-on oversight of GMP facilities, Ensure hands-on oversight of GMP equipment, Provide leadership to staff, Provide guidance to staff, Provide direction to staff, Evaluate and sign off compliance documentation, Approve regulatory filings, Oversee external batch record review, Ensure proper batch release documentation, Approve manufacturing records, Approve aseptic filling records, Organize investigations, Complete investigations, Coordinate investigations with departments, Drive investigation closure, Conduct GxP Auditing for providers, Prepare for audits, Execute audits, Write audit reports, Follow up on audit findings, Ensure adherence to GxP requirements, Ensure adherence to SOPs, Oversee relationship with Qualified Person, Direct work requiring QP oversight, Direct work requiring QP disposition", "teamCollaboration" : "Cross-functional teams; Program teams; External partners; Vendors", "domainKnowledge" : "cGMP; GxP systems; Drug substance manufacture; Drug product manufacture", "domainList" : [ "cgmp", "gxp-systems", "drug-substance-manufacture", "drug-product-manufacture" ], "domainSpecificKnowledge" : [ "cGMP", "GxP systems", "Drug substance manufacture", "Drug product manufacture" ], "communicationSkills" : "Verbal communication; Written communication", "documentationSkills" : "Compliance documentation; Regulatory filings; Batch records; Audit reports", "problemSolvingSkills" : "Risk analysis; Root cause analysis", "outcomesObjectives" : "Ensure timely product release; Drive timely investigation closure", "qualificationsBasic" : "Bachelors or Advanced degree in scientific discipline, 15+ years pharmaceutical/biotech industry experience, 7+ years Quality management experience, Experience in auditing/vetting of CDMOs, Understanding of worldwide cGMP requirements, Experience interacting with regulatory health authorities", "qualificationsPreferred" : "CT/GTiologics experience", "remoteFriendly" : true, "workSiteFlexibility" : "Onsite", "rawDescription" : "Company Overview: Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases. Position Overview: The Senior Director, Product Quality Assurance, Cambridge (PQA) will be responsible for creating/monitoring and maintaining phase appropriate levels of compliance in all of our CDMOs/external partners. The position will be critical to the overall build strategy and growth of the Quality organization for Beam as the company grows and evolves from a Research and Discovery company to a broader organization moving products through the clinical pipeline to commercial launch and growth. The position will have overall responsibility to ensure initiatives related to quality and compliance are optimized and executed appropriately in the areas of GMP compliance with Beam’s externally focused manufacturing efforts. Position will also provide top level guidance and support on internal GMP activities in the Cambridge location, and globally from a GMP perspective. Primary Responsibilities: Primary responsibilities encompass all aspects of Quality support for GMP operations. Quality oversight will primarily encompass external GMP operations (ex. CDMOs) and QC support in Cambridge. Responsibilities for quality oversight will also extend to support in other areas of Beam that may support GMP activities. Responsible as a key relationship manager CDMOs/external partners from a quality perspective. Works cross-functionally with other members of the greater CMC area and program teams for CDMO selection and vetting. Establishes an overall KPI and metrics program to assist in governing the CDMO relationships. Establishes a routine process for continuous improvement of the CDMO oversight processes. Define clear Quality objectives and ensure progress and cross-functional completion of responsibilities; use judgment to develop solutions and drive risk analysis and mitigation strategies. Create and ensure appropriate quality systems are in place to support product release in a compliant and timely manner and routinely monitor performance to established targets. Ensure appropriate systems are in place for follow up and closing investigations and audit observations. Ensure that exceptions are analyzed for corrective preventive actions and product impact. Provide technical expertise for product quality decisions. Evaluate facility, procedures, equipment, personnel and processes to ensure that they consistently deliver product that meets all applicable requirements. Oversee all aspects of Quality related to the manufacture of products externally. Oversee Quality support for QC activities in Cambridge, including testing, method qualification/validation, instrument qualification, and quality system records related to QC activities. Ensure Quality hands-on oversight of GMP-relevant facilities and equipment in Cambridge. Provide leadership, guidance, and direction to staff consistent with cGMP. Evaluate and sign off on compliance documentation including approving regulatory filings for designated products as required. Oversee external batch record review and ensure proper batch release documentation. Assure appropriate reviews and approvals of manufacturing and aseptic filling records for execution as well as for product release. Take lead role in organizing and completing investigations, coordinating with other departments involved and driving closure in a timely manner. Provide GxP Auditing for contract service providers including audit preparation, execution of the audit, the audit report, and follow up to any finding(s). Ensure adherence to GxP requirements and SOPs. Oversee relationship with Qualified Person (QP) and direct work requiring QP oversight and disposition. Embodies Beam’s cultural values and aligns daily actions with departmental goals and company culture. Qualifications: Bachelors or Advanced degree in a scientific discipline. 15+ years’ experience in the pharmaceutical/biotech industry in combination with drug substance/drug product manufacture, development and quality. Must have CT/GT/biologics experience. 7+ years of Quality management experience with a successful track record in managing CDMOs as well as internal QA systems in a virtual environment. Experience in auditing/vetting of CDMOs. Understanding of worldwide requirements of cGMP and quality systems for commercial and clinical products. Excellent verbal and written communication skills, detail-oriented personality and ability to work and drive change across functions. Experience interacting with regulatory health authorities at pre- and post-approval inspection. Established expertise and training in GxP systems. Ability to evaluate Quality Systems and drive value added enhancements. Strong team player that has a customer service approach and is solution oriented. Attention to detail and the ability to work individually, within a multi-disciplinary team, as well as with external partners and vendors. Excellent team building, leadership and management skills. Excellent listening, communication and interpersonal skills fostering team spirit. Consistent delivery of high quality work at all times. Outstanding skills in managing vendors and others involved in Quality and Regulatory activities to meet corporate objectives. The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data. Beam Pay Range $260,000—$320,000 USD", "summaryDescription" : "Senior Director, Product Quality Assurance at Beam Therapeutics. Skills: Product Quality Assurance, GMP Compliance, CDMO Oversight. Create compliance levels in CDMOs. Monitor compliance levels in CDMOs", "postedDate" : "2026-06-11T22:41:39.539", "createdAt" : "2026-06-11T22:41:39.539", "lastUpdated" : "2026-06-14T20:41:25.136", "ingestTimestamp" : "2026-06-11T22:41:39.539", "mongoId" : "6a2ac53174d8ee00a0700b87", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 260000, "salaryAnnualMax" : 320000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Drug substance manufacture", "Drug product manufacture", "Method validation", "Instrument qualification", "Batch record review", "Audit preparation", "Leadership", "Critical thinking", "Product Quality Assurance", "GMP Compliance", "CDMO Oversight", "Quality assurance", "GMP compliance", "CDMO management", "Quality systems", "Risk analysis", "Product release", "Regulatory filings", "GxP Auditing", "Quality oversight", "cGMP", "GxP systems" ], "skillCount" : 22, "jobCategory" : "other", "jobSubcategory" : "quality", "dataQualityScore" : 1.0, "_score" : 749.9848, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotechnology" }, { "id" : "6a2c798e74d8ee00a0941d7a", "title" : "Director, Quality", "company" : "Fanatics Collectibles", "industry" : "Retail", "salary" : { "min" : 215000.0, "max" : 305000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Director of Quality in the Retail industry in Sunnyvale, United States, adjusted for seniority and company size." }, "location" : "Sunnyvale, Texas, United States", "locations" : [ "Sunnyvale", "Texas", "United States" ], "timestamp" : "2026-06-15T09:35:56.404", "fingerprint" : "b8c61e115ef4db5e1fac45c54c4b108a006bb1bd9cd554b1b5893755be6e450e", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/fanaticscollectibles/jobs/4209042009", "externalId" : "4209042009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Sunnyvale", "state" : "Texas", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "32.7965165,-96.5608242" } ], "locationText" : "Sunnyvale, Texas, United States", "experienceLevel" : "Director", "technicalSkills" : "MS Office, Airtable", "professionalSkills" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement", "Issue Resolution", "Root Cause Analysis", "Risk Management", "Audit Management" ], "hardSkillsList" : [ "Quality control systems", "SOPs", "Work instructions", "Training material implementation", "8D", "5 Whys", "Fishbone", "Process improvement", "Process optimization", "KPI reporting", "Scorecard reporting" ], "hardSkills" : [ { "name" : "Quality control systems", "level" : "intermediate" }, { "name" : "SOPs", "level" : "intermediate" }, { "name" : "Work instructions", "level" : "intermediate" }, { "name" : "Training material implementation", "level" : "intermediate" }, { "name" : "8D", "level" : "intermediate" }, { "name" : "5 Whys", "level" : "intermediate" }, { "name" : "Fishbone", "level" : "intermediate" }, { "name" : "Process improvement", "level" : "intermediate" }, { "name" : "Process optimization", "level" : "intermediate" }, { "name" : "KPI reporting", "level" : "intermediate" }, { "name" : "Scorecard reporting", "level" : "intermediate" } ], "majorSkills" : "Quality Management System, Operational excellence, Process improvement, Supplier quality", "majorSkillsList" : [ "Quality Management System", "Operational excellence", "Process improvement", "Supplier quality" ], "coreResponsibilities" : "Develop Quality Management System, Oversee Quality Management System, Ensure product quality standards, Ensure product integrity standards, Ensure product timeliness standards, Focus on process quality, Focus on quality at internal partners, Focus on quality at external partners, Align quality goals with Production, Align quality goals with Continuous Improvement, Align quality goals with Innovation, Align quality goals with Engineering, Align quality goals with Supply Chain, Troubleshoot production issues, Implement effective solutions, Address prepress file issues, Address proofing issues, Address stock issues, Address specification issues, Curate department records, Update department records, Support KPI reporting development, Support analytics development, Track performance indicators, Use performance data, Provide weekly scorecards, Provide monthly scorecards, Ensure compliance with safety protocols, Monitor machinery, Inspect WIP, Handle materials", "teamCollaboration" : "Cross-functional teams; External partners; Internal product teams; Supply chain", "projectManagementSkills" : [ "Project charters", "Project deliverables" ], "domainKnowledge" : "Print manufacturing; Pack outs; Manufacturing environment", "domainList" : [ "print-manufacturing", "pack-outs", "manufacturing-environment" ], "domainSpecificKnowledge" : [ "Print manufacturing", "Pack outs", "Manufacturing environment" ], "toolProficiency" : [ "SAP", "Oracle", "MS Word", "MS Excel", "MS PowerPoint" ], "communicationSkills" : "Written skills; Verbal skills", "problemSolvingSkills" : "Issue Resolution; Root Cause Analysis; Troubleshoot production issues", "specialRequirements" : "Travel <20%, Work extended hours, Work overtime, Work evenings, Work weekends, Work holidays, Regular bending, Stooping, Kneeling, Tolerance for dust, Tolerance for fumes, Tolerance for odors, Alertness during long shifts, Focus during high-pressure situations", "outcomesObjectives" : "Improve production performance; Make informed decisions; Drive continuous improvement", "qualificationsBasic" : "Bachelor's degree in engineering, 10-15 years quality assurance experience, 5 years senior leadership experience, Mastery of Six Sigma, Mastery of Lean Manufacturing, Mastery of Statistical Process Controls, Experience conducting quality process audits, Experience managing supplier relationships", "qualificationsPreferred" : "Experience in Trading Card Games, Experience in Collectibles, CMQ/OE certification, CQA certification, Lean Six Sigma Green Belt, Lean Six Sigma Black Belt", "workSiteFlexibility" : "Onsite", "rawDescription" : "About Us Fanatics is building a leading global digital sports platform. We ignite the passions of global sports fans and maximize the presence and reach for our hundreds of sports partners globally by offering products and services across Fanatics Commerce, Fanatics Collectibles, and Fanatics Betting collect physical and digital trading cards, sports memorabilia, and other digital assets; and bet as the company builds its Sportsbook and iGaming platform. Fanatics has an established database of over 100 million global sports fans; a global partner network with approximately 900 sports properties, including major national and international professional sports leagues, players associations, teams, colleges, college conferences and retail partners, 2,500 athletes and celebrities, and 200 exclusive athletes; and over 2,000 retail locations, including its Lids retail stores. Our more than 22,000 employees are committed to relentlessly enhancing the fan experience and delighting sports fans globally. About the Team Fanatics Collectibles is a new company operating at the intersection of collectibles, culture, and technology. Backed by world-class investors, operators, and sports & entertainment partners, we are building the global leader in next-generation collectibles. As part of the broader Fanatics ecosystem, we leverage a digital sports platform that spans over 900 sports properties and engages more than 81 million fans. Together, we are reimagining every part of the collectibles experience for fans, partners, and creators. Role Summary This is a senior leadership role responsible for the strategic development and operational oversight of the company’s Quality Management System and upholding Fanatic Collectibles core pillar – Relentlessly Improving the Collectors Experience. The Director, Quality Assurance ensures that all Topps and Fanatics Collectibles products are manufactured to the highest standards of quality, integrity, and timeliness. The Director will focus on process and quality at internal and external partners with regards to operational excellence, print, finishing and pack outs. This position interfaces with a range of internal product development teams and the breadth of our external supply chain. The Director, Quality Assurance reports directly to the Vice President of Quality Assurance and Compliance. Ability to work extended hours, including overtime, evenings, weekends, and holidays as production demands. Experience in Trading Card Games or Collectibles a plus This position is in Sunnyvale, TX Travel <20% Experience/Education: Bachelor’s degree in engineering (Mechanical, Industrial or Manufacturing), Quality Management or related fields. 10-15 years or progressive experience in quality assurance, with at least 5 years in a senior leadership or directorial capacity. Certifications are a MAJOR plus - CMQ/OE, CQA, Lean Six Sigma – Green or Black Belt Quality Assurance Experience: Experience in developing and maintaining quality control systems Mastery of Six Sigma, Lean Manufacturing, and Statistical Process Controls (SPC) is essential. Proven ability to implement quality assurance and ensure compliance within set standards Proven ability to work cross functionally to define quality parameters, align SOP’s, work instructions, training material and implementation Experience with conducting quality process audits and addressing safety, security and quality issues at suppliers. Management Experience: Significant experience in a managerial or supervisory role within a busy manufacturing setting – the current operation is 24/7 across multiple sites. Experience leading and developing a team. Proven ability to manage and optimize resources effectively. Process Improvement Experience: Expertise in Issue Resolution, Root Cause Analysis using techniques like 8D, 5 Whys and Fishbone. Demonstrated experience in process improvement and optimization. Track record of implementing successful process improvement initiatives. Proficiency in Risk Management. Audit Management – Proven ability to lead internal and external audits. Collaboration and Cross-Functional Experience: Experience working with cross-functional teams to achieve production goals. Proven ability to work effectively with other departments, such as engineering, quality assurance, and supply chain. Experience in managing supplier relationships and coordinating with external partners Essential Functions and Responsibilities: Supervision and Leadership: Cross-Functional Collaboration:Ability to align quality goals with Production, Continuous Improvement, Innovation, Engineering, and Supply Chain Ability to troubleshoot production issues and implement effective solutions onsite at suppliers with regards to prepress files, proofing, stock, specification issues, etc. Innovative thinking to improve current production processes Team Development:Experience in recruiting, mentoring, and managing a high-performing team of quality managers, supervisors, and technicians. Conflict resolution and team-building abilities Excellent interpersonal communication skills Strong decision-making capabilities Strong organizational and time management skills Supplier Quality Management:Establishing standards for the supply chain, including supplier audits and qualification Ensure external partners have clear direction with regards to Quality Standards and parameters. Proven ability to lead and motivate suppliers Quality Control: Attend product engineering and BOM (Bill of Material) reviews, evaluate risks and inefficiencies, and communicate with the product development team to drive efficiency, meet quality standards, provide cost and time savings. Ability to implement and monitor quality assurance programs. Works cross functionally to manage on-site and in-process quality assurance checks for all WIP and finished goods across supply chain. Collaborate with the Fanatics Collectibles team to understand challenges and pain points in the supply chain and develop and execute plans to address ongoing issues and concerns with suppliers. Ensure 1st Articles for each discipline meets quality specifications for responsible department. Identify and resolve production and quality issues within the time frame of job schedule for responsible department. Strong understanding of quality with regards to industry standards. Safety and Compliance: Ensure compliance with all regulatory and company standards for all printed work. Knowledge of ISO standards and regulatory compliance. Continuous Improvement: Identify areas/opportunities for improvement with regards to production process. Develop and coordinate the research and execution of cost reduction and efficiency improvement projects at suppliers for Fanatics Collectibles. Use data-driven approaches to enhance production performance and reduce waste. Identify areas for improvement in production processes and implement changes. Develop and build out the revised standard operating procedures (SOPs) & Quality Control processes in partnership with vendors and internal SMEs to enhance efficiency and productivity. Reporting and Documentation: Maintain accurate and updated records of department production activities, organization charts and initiatives, including project charters, ownership and deliverables. Proficiency in data and analytics - support the development of KPI reporting & analytics (scrap, defect rates, cost of quality, efficiency, equipment & headcount utilization, etc.). Track key performance indicators (KPIs) to measure and improve production performance. Use performance data to make informed decisions and drive continuous improvement initiatives. Provide weekly and monthly scorecards showing cost of quality, remake and rework KPIs. Additional Skills: Proficiency in manufacturing software (e.g., WMS, ERP systems like SAP, Oracle). Proficient in MS Office (Word, Excel, PowerPoint, etc.), Airtable Data driven, highly analytical, ability to analyze and interpret production data to identify trends and areas for improvement. Strong understanding of process optimization and efficiency improvement. Excellent written and verbal skills Bilingual a plus PHYSICAL DEMANDS Regular bending, stooping, and kneeling to monitor machinery, inspect WIP, and handle materials. Compliance with all safety protocols and regulations regarding PPE usage (including safety glasses, gloves, ear protection, etc.) as needed. Exposure to a manufacturing environment with varying temperatures, noise levels, and potential hazards. Tolerance for working in conditions that may include dust, fumes, and strong odors. Ability to remain alert and focused during long shifts and high-pressure situations. Ensure your Fanatics job offer is legitimate and don’t fall victim to fraud. Fanatics never seeks payment from job applicants. Feel free to ask your recruiter for a phone call or other type of communication for interview, and ensure your communication is coming from a Fanatics email address (including @collectfanatics.com). For added security, where possible, apply through our company website at www.fanaticsinc.com/careers By submitting your application, you agree to our terms of service and acknowledge you have read our Candidate Privacy Policy.", "summaryDescription" : "Director, Quality at Fanatics Collectibles. Skills: Quality Management System, Operational excellence, Process improvement, Supplier quality. Develop Quality Management System. Oversee Quality Management System", "postedDate" : "2026-06-13T20:22:38.566", "createdAt" : "2026-06-13T20:22:38.566", "lastUpdated" : "2026-06-15T09:35:56.404", "ingestTimestamp" : "2026-06-13T20:22:38.566", "mongoId" : "6a2c798e74d8ee00a0941d7a", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 215000, "salaryAnnualMax" : 305000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Quality control systems", "SOPs", "Work instructions", "Training material implementation", "8D", "5 Whys", "Fishbone", "Process improvement", "Process optimization", "KPI reporting", "Scorecard reporting", "Quality Management System", "Operational excellence", "Supplier quality", "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement", "Issue Resolution", "Root Cause Analysis", "Risk Management", "Audit Management", "Project charters", "Project deliverables", "Print manufacturing", "Pack outs", "Manufacturing environment", "SAP", "Oracle", "MS Word", "MS Excel", "MS PowerPoint" ], "skillCount" : 35, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 749.02625, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Retail", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c7b8374d8ee00a0949f81", "title" : "Quality Assurance Manager", "company" : "ThermalWorks LLC", "industry" : "Manufacturing", "salary" : { "min" : 115000.0, "max" : 165000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Manager in Quality Assurance in the United States, adjusted for remote work and the manufacturing industry." }, "location" : "Remote - US", "locations" : [ "Remote - US" ], "timestamp" : "2026-06-16T02:28:27.969", "fingerprint" : "8a38d7c246620d98b3d0342e0a93a4c5b4e893dad67d5d0f28b559fa2a855bda", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/li-thermal-works/jobs/4257576009", "externalId" : "4257576009", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Manager", "technicalSkills" : "Hydronic cooling, Chiller platforms, Data center infrastructure, HVAC, Mechanical systems, Controls integration, BASMS platforms", "professionalSkills" : [ "Quality control", "Quality assurance", "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement" ], "hardSkillsList" : [ "Assembly inspection", "Wiring inspection", "Piping inspection", "Commissioning inspection", "Service inspection", "Mechanical system assessment", "Equipment startup assessment" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Assembly inspection", "level" : "intermediate" }, { "name" : "Wiring inspection", "level" : "intermediate" }, { "name" : "Piping inspection", "level" : "intermediate" }, { "name" : "Commissioning inspection", "level" : "intermediate" }, { "name" : "Service inspection", "level" : "intermediate" }, { "name" : "Mechanical system assessment", "level" : "intermediate" }, { "name" : "Equipment startup assessment", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "Quality assurance, Mechanical systems, Data center infrastructure, Factory operations", "majorSkillsList" : [ "Quality assurance", "Mechanical systems", "Data center infrastructure", "Factory operations" ], "coreResponsibilities" : "Conduct factory walkthroughs, Identify quality concerns, Review assembly documentation, Review wiring documentation, Review piping documentation, Review commissioning documentation, Coordinate findings with factory leadership, Flag hold conditions, Document inspection outcomes, Provide written reports, Perform field QA/QC inspections, Verify equipment installation, Verify commissioning work, Verify service work, Assess mechanical system performance, Assess hydronic loop integrity, Assess refrigerant circuit health, Assess controls integration, Assess equipment startup, Coordinate site access, Coordinate scheduling, Generate inspection reports, Document findings, Document nonconformances, Document corrective actions, Track resolution status, Participate in QC meetings, Present findings and trends, Maintain log of open quality items, Track status through closure, Surface recurring field issues, Support development of inspection checklists, Support refinement of MOPs, Support refinement of SOPs, Support refinement of QA/QC documentation standards", "teamCollaboration" : "Factory leadership coordination; Field operations coordination; Tech support interface; Quality and service leadership", "domainKnowledge" : "Hydronic cooling; Chiller platforms; Data center infrastructure; HVAC systems; Mechanical systems; Cooling towers; Controls integration; Critical infrastructure", "domainList" : [ "hydronic-cooling", "chiller-platforms", "data-center-infrastructure", "hvac-systems", "mechanical-systems", "cooling-towers", "controls-integration", "critical-infrastructure" ], "domainSpecificKnowledge" : [ "Hydronic cooling", "Chiller platforms", "Data center infrastructure", "HVAC systems", "Mechanical systems", "Cooling towers", "Controls integration", "Critical infrastructure" ], "toolProficiency" : [ "BASMS platforms" ], "communicationSkills" : "Present findings; Written reports", "documentationSkills" : "Inspection reports; Nonconformance logs; Findings summaries; Quality documentation standards", "problemSolvingSkills" : "Root cause analysis", "specialRequirements" : "50-65% travel", "qualificationsBasic" : "7+ years HVAC/mechanical systems experience, QA/QC experience on construction/commissioning/service projects, Read and interpret engineering drawings, Read and interpret submittals, Read and interpret MOPs, Read and interpret SOPs, Read and interpret EAPs, Written documentation skills", "qualificationsPreferred" : "Turbocor centrifugal chiller platforms experience, Dry cooler or adiabatic cooling systems familiarity, Presenting quality findings to management, Instructor-level training background, Technical mentorship background, Review RFIs experience, Review equipment submittals experience", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Opportunity ThermalWorks LLC is seeking an experienced Quality Assurance Manager to serve as the technical quality authority across our factory operations, customer field sites, and internal quality control function. This is a cross-functional, high-visibility role that sits at the intersection of manufacturing, field service, and quality leadership. The ideal candidate brings deep hands-on experience with mission-critical mechanical systems — particularly hydronic cooling, chiller platforms, and data center infrastructure — combined with the discipline and communication skills to document findings clearly and present them to leadership. This is not a desk role. The person in this seat will be in the factory, in the field, and in the meeting room. This role has a travel requirement of 50-65%. Key Responsibilities Include but are not limited to: Factory Quality (2–3 Visits per Production Cycle) Conduct structured walkthroughs of ThermalWorks manufacturing operations to identify quality concerns before units ship Review assembly, wiring, piping, and commissioning documentation against engineering specifications and approved submittals Coordinate findings with factory leadership and flag hold conditions requiring resolution prior to release Document inspection outcomes and provide written reports to the Director of Quality Field Quality Inspections Perform on-site QA/QC inspections at customer data center locations to verify ThermalWorks equipment installation, commissioning, and service work meets required standards Assess mechanical system performance against design intent including hydronic loop integrity, refrigerant circuit health, controls integration, and equipment startup Coordinate site access and scheduling with field operations leadership Generate structured inspection reports for each site visit, documenting findings, nonconformances, corrective actions required, and status of resolution Quality Control Meetings & Reporting Participate in internal QC meetings as the field and factory intelligence source, presenting findings and trends to quality and service leadership Maintain a running log of open quality items across factory and field, tracking status through closure Collaborate with the tech support group to surface recurring field issues that may indicate systemic quality or design concerns Support the development and refinement of inspection checklists, MOPs, SOPs, and QA/QC documentation standards Director of Quality Primary reporting relationship. Drives QC meeting participation, documentation standards, and quality findings escalation. Field Operations Coordinates site scheduling, field logistics, and alignment with field service teams during on-site inspections. Tech Support Interfaces on technical issue resolution, recurring fault patterns, and field support coverage. Factory Leadership Engages during factory visits for inspection coordination, build quality review, and pre-shipment hold authority. Education and Experience Required 7+ years of hands-on experience with commercial or mission-critical HVAC/mechanical systems including chillers, hydronic loops, cooling towers, and associated controls Demonstrated QA/QC experience on construction, commissioning, or service projects in data center or critical infrastructure environments Ability to read and interpret engineering drawings, submittals, MOPs, SOPs, and EAPs Strong written documentation skills — inspection reports, nonconformance logs, and findings summaries must be clear and actionable Willingness and ability to travel to factory and field sites on a regular basis Proficiency with BAS/BMS platforms for system verification during site inspections Preferred Experience with Turbocor centrifugal chiller platforms Familiarity with dry cooler or adiabatic cooling systems Prior experience presenting quality findings to management-level audiences Background in instructor-level training or technical mentorship Experience reviewing RFIs and equipment submittals This position is structured for a senior technical professional who wants more than a wrench and a work order. You will be the quality intelligence function for ThermalWorks — the person who sees our product built, sees it in the field, and has a seat at the table where quality decisions get made. Your findings carry weight. Your reports go to leadership. Your site visits carry the authority of the Quality Control function. ThermalWorks is a fast-growing manufacturer of adaptive dry cooling systems for hyperscale data center applications, operating within a vertically integrated infrastructure platform. This is a ground-floor opportunity to build a quality function that scales with the business. About Our Parent Company, Endeavour Endeavour is rethinking the infrastructure model for the benefit of all. Instead of relying on big, centralized systems that often leave communities locked into outdated networks, we are building an integrated technology stack using modular components that can be repeated and scaled. Operating as a purpose trust, we create a continual cycle of innovation by investing in breakthrough technologies to build faster, cleaner infrastructure for data, energy, materials, and water. We tackle the industry’s most complex challenges by deploying scalable, modular solutions across the AI ecosystem—including carbon-neutral energy and revolutionary data center cooling. Our team of passionate changemakers is driven by a shared mission to build regenerative systems that give back more than they take. To work at Endeavour is to collaborate with proven experts, cut through the unnecessary to get things done, and know you are making a lasting impact on people and the planet. Position: Quality Assurance Manager Full-Time or Part-Time: Full-Time Reports to: Director of Quality Location: Remote - US Contact: recruiting@endeavourii.com", "summaryDescription" : "Quality Assurance Manager at ThermalWorks LLC. Skills: Quality assurance, Mechanical systems, Data center infrastructure, Factory operations. Conduct factory walkthroughs. Identify quality concerns", "postedDate" : "2026-06-14T20:10:39.497", "createdAt" : "2026-06-14T20:10:39.497", "lastUpdated" : "2026-06-16T02:28:27.969", "ingestTimestamp" : "2026-06-14T20:10:39.497", "mongoId" : "6a2c7b8374d8ee00a0949f81", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 115000, "salaryAnnualMax" : 165000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Assembly inspection", "Wiring inspection", "Piping inspection", "Commissioning inspection", "Service inspection", "Mechanical system assessment", "Equipment startup assessment", "Leadership", "Quality assurance", "Mechanical systems", "Data center infrastructure", "Factory operations", "Quality control", "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement", "Hydronic cooling", "Chiller platforms", "HVAC systems", "Cooling towers", "Controls integration", "Critical infrastructure", "BASMS platforms" ], "skillCount" : 27, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Manager", "dataQualityScore" : 1.0, "_score" : 746.33606, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Manufacturing", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c8ca774d8ee00a097601f", "title" : "Quality Assurance Technician", "company" : "Kevin's Natural Foods", "industry" : "Quality Assurance", "salary" : { "min" : 22.0, "max" : 30.0, "currency" : "USD", "frequency" : "Yearly" }, "location" : "Mariposa Manufacturing Facility & Office", "locations" : [ "Mariposa Manufacturing Facility & Office" ], "timestamp" : "2026-06-16T02:47:08.690", "fingerprint" : "d8bfde8f06e4a31ce822e51b1d215cf2ed3aaa6fcb174668cfbed73139fe86f1", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/kevins-natural-foods/34929568-1e41-400b-ab55-d52bec7c30b6/application", "externalId" : "34929568-1e41-400b-ab55-d52bec7c30b6", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Mariposa", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "37.5701480,-119.9036592" } ], "locationText" : "Mariposa, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 1, "experienceMaxYears" : 3, "professionalSkills" : [ "Quality control", "Process improvement" ], "hardSkillsList" : [ "Quality assurance", "Food safety" ], "hardSkills" : [ { "name" : "Quality assurance", "level" : "intermediate" }, { "name" : "Food safety", "level" : "intermediate" } ], "majorSkills" : "Quality assurance, Food safety", "majorSkillsList" : [ "Quality assurance", "Food safety" ], "coreResponsibilities" : "Perform quality checks on raw materials, Monitor production processes, Conduct finished product testing, Document quality control findings, Identify and report deviations, Assist with process improvement initiatives, Maintain a clean and organized work area, Follow all safety and sanitation procedures", "teamCollaboration" : "Production team; Quality department", "domainKnowledge" : "Food safety regulations; Manufacturing processes", "domainList" : [ "food-safety-regulations", "manufacturing-processes" ], "domainSpecificKnowledge" : [ "Food safety regulations", "Manufacturing processes" ], "toolProficiency" : [ "Microsoft Office Suite" ], "communicationSkills" : "Reporting findings", "documentationSkills" : "Quality records", "problemSolvingSkills" : "Root cause analysis", "specialRequirements" : "Must wear safety shoes, Must wear safety glasses", "outcomesObjectives" : "Ensure product quality; Maintain compliance", "qualificationsBasic" : "High school diploma or GED, 1 year of experience in a manufacturing environment, Ability to lift 50 pounds", "qualificationsPreferred" : "Experience with HACCP, Forklift certification", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "What You’ll Do: - Responsible for monitoring, and programing critical control points (CCP), product food safety and quality throughout the manufacturing process. - Responsible for performing sanitation verification and allergen testing on equipment and other areas required. - Responsible for the correct recording and filing of all relevant record logs and documentation. - Ensures the correct recipe guidelines for products are met during processing. - Work closely with production staff to maintain and education in the areas of sanitation, hygiene, GMP’s and other food safety guidelines. - Responsible to issue disciplinary action when directed. - Collect product samples for product development, lab retains, and the laboratory when directed. - Perform inspections on products, equipment, and machinery. - Other duties and projects as assigned by QA Management. What You’ll Need: - 1-3 years’ experience in a food processing environment. - 2+ years’ experience in a meat or poultry processing environment preferred. - Bachelor of Science Degree or Diploma in Microbiology or food science. - Knowledge of HACCP, GMP’s, allergens, and food defense - HACCP Certification. - Proficient computer skills and Microsoft Office Applications (Outlook, Word, and Excel) - Excellent interpersonal, verbal, and written communication and problem-solving skills - Bilingual (Spanish) a plus. - Flexibility and ability to work mandatory overtime and weekends as needed. Healthy, Diverse Teams Breed Innovation: Kevin’s Natural Foods is proud to be an equal opportunity employer. We deeply believe that diverse backgrounds and experiences make better teams, and we seek to attract talent from all walks of life. The team at Kevin’s is smart, humble, and passionate and we value a work environment that fosters personal development and opportunities to move within our small, but quickly growing organization. More About Kevin’s Natural Foods: Kevin’s Natural Foods is a line of healthy entrées, sides, and sauces, on a mission to make clean eating delicious and accessible. Kevin’s guilt-free, sous-vide entrées and sides, and signature certified paleo, keto, and gluten-free sauces allow health-conscious home cooks to whip up delicious meals in five minutes or less. With restaurant-quality ingredients and recipes, Kevin’s products are readily available on the shelves at leading grocery retailers nationwide including Costco, Whole Foods, Albertsons, HEB and Publix. All Kevin’s products contain no refined sugar, artificial ingredients, grains, or soy, and are made with antibiotic- and hormone-free meat. A true market disruptor, Kevin’s Natural Foods is the first clean refrigerated entrée brand. Healthy, Diverse Teams Breed Innovation: Kevin’s Natural Foods is proud to be an equal opportunity employer. We deeply believe that diverse backgrounds and experiences make better teams, and we seek to attract talent from all walks of life. The team at Kevin’s is smart, humble, and passionate and we value a work environment that fosters personal development and opportunities to move within our small, but quickly growing organization. More About Kevin’s Natural Foods: Kevin's Natural Foods is a line of refrigerated and frozen meals, sides, soups, and sauces on a mission to empower even the busiest people to eat clean without sacrificing flavor. Co-founded by Kevin McCray who battled an auto-immune disorder for years, Kevin's Natural Foods was born from his desire to make clean eating seamlessly fit into any lifestyle. Shockingly delicious and made with clean ingredients, Kevin’s products are ready in minutes and always free from gluten, soy, and refined sugar. In 2023, Kevin’s Natural Foods joined the Mars Food & Nutrition family, allowing us to expand our reach, accelerate innovation, and bring our mission to even more households while staying true to the quality and integrity that define our brand. A true market disruptor, Kevin's is the first clean refrigerated entrée brand working to prove every day that proper nutrition can be as delicious as it is healthy. The pay range for this role is $20.00- $30.00 per hour + benefits Kevin's Natural Foods uses E-verify to confirm employment eligibility. For more information, please see the links below: https://www.everify.gov/sites/default/files/everify/posters/IER_RightToWorkPoster%20Eng_Es.pdf https://www.everify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf", "summaryDescription" : "Quality Assurance Technician at Kevin's Natural Foods. Skills: Quality assurance, Food safety. Perform quality checks on raw materials. Monitor production processes", "createdAt" : "2026-06-14T19:28:14.590", "lastUpdated" : "2026-06-16T02:47:08.690", "ingestTimestamp" : "2026-06-14T19:28:14.590", "mongoId" : "6a2c8ca774d8ee00a097601f", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMax" : 30, "salaryBand" : "<30k", "hasSalary" : false, "allSkills" : [ "Quality assurance", "Food safety", "Quality control", "Process improvement", "Food safety regulations", "Manufacturing processes", "Microsoft Office Suite" ], "skillCount" : 7, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.7777778, "_score" : 739.0993, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Food & Beverage", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c92ee74d8ee00a0986e48", "title" : "Senior Analytics Engineer (GCP)", "company" : "Xebia", "industry" : "Consulting", "salary" : { "min" : 200000.0, "max" : 320000.0, "currency" : "PLN", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for Senior Analytics Engineer (GCP) in Poland, adjusted for seniority and industry." }, "location" : "Poland", "locations" : [ "Poland" ], "timestamp" : "2026-06-15T09:08:57.221", "fingerprint" : "76f56fb3606d87c6b0fe7e2a25720df5ef1e13226f275fa00ab33ee620447456", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/xebiacee/jobs/6003535004", "externalId" : "6003535004", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Poland", "continent" : "eu", "workMode" : "onsite" } ], "locationText" : "Poland", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "SQL, Dbt, Dataform, GCP, BigQuery, Cloud Storage, Composer, Airflow, Data pipelines, ETL, ELT, CI/CD, Terraform, GitHub Actions, Cloud Build, Pub/Sub, Datastream, Dataflow, Knowledge Catalog, Python, AWS, Azure, Databricks, Snowflake, AI, ML", "professionalSkills" : [ "Data modeling", "Data transformation", "Data quality", "Data validation", "Data migration", "Analytics engineering", "Data product development", "Business needs translation" ], "hardSkillsList" : [ "Dimensional modeling", "Data marts", "ETL/ELT processes", "Data validation", "Data testing", "Data quality", "CI/CD", "Data governance", "Data cataloging", "Data lineage", "Streaming data processing", "AI/ML use cases", "Analytics enablement" ], "hardSkills" : [ { "name" : "Dimensional modeling", "level" : "intermediate" }, { "name" : "Data marts", "level" : "intermediate" }, { "name" : "ETL/ELT processes", "level" : "intermediate" }, { "name" : "Data validation", "level" : "intermediate" }, { "name" : "Data testing", "level" : "intermediate" }, { "name" : "Data quality", "level" : "intermediate" }, { "name" : "CI/CD", "level" : "intermediate" }, { "name" : "Data governance", "level" : "intermediate" }, { "name" : "Data cataloging", "level" : "intermediate" }, { "name" : "Data lineage", "level" : "intermediate" }, { "name" : "Streaming data processing", "level" : "intermediate" }, { "name" : "AI/ML use cases", "level" : "intermediate" }, { "name" : "Analytics enablement", "level" : "intermediate" } ], "majorSkills" : "Analytics Engineering, GCP, BigQuery, Dbt", "majorSkillsList" : [ "Analytics Engineering", "GCP", "BigQuery", "Dbt" ], "coreResponsibilities" : "Design data models, Build data models, Maintain data models, Develop analytical datasets, Optimize analytical datasets, Develop data marts, Collaborate with data engineers, Collaborate with business stakeholders, Translate requirements, Implement data transformation logic, Ensure data quality, Ensure data testing, Ensure data validation, Support pipeline migration, Work with ingestion pipelines, Ensure alignment with reporting needs, Contribute to governance, Contribute to data cataloging, Contribute to lineage, Enable self-service analytics, Validate data consistency, Support cutover, Support BI layer, Ensure KPI consistency, Participate in establishing best practices", "teamCollaboration" : "Data engineers; Business stakeholders", "projectManagementSkills" : [ "CI/CD" ], "domainKnowledge" : "Data modeling; Lakehouse architectures; Data pipelines; ETL/ELT processes; Data governance; Data cataloging; Data lineage; Streaming data; Near real-time data; AI/ML use cases; Analytics enablement; FinOps; Cost optimization", "domainList" : [ "data-modeling", "lakehouse-architectures", "data-pipelines", "etl-elt-processes", "data-governance", "data-cataloging", "data-lineage", "streaming-data", "near-real-time-data", "ai-ml-use-cases", "analytics-enablement", "finops", "cost-optimization" ], "domainSpecificKnowledge" : [ "Data modeling", "Lakehouse architectures", "Data pipelines", "ETL/ELT processes", "Data governance", "Data cataloging", "Data lineage", "Streaming data", "Near real-time data", "AI/ML use cases", "Analytics enablement", "FinOps", "Cost optimization" ], "toolProficiency" : [ "Dbt", "Dataform", "BigQuery", "Cloud Storage", "Composer", "Airflow", "Terraform", "GitHub Actions", "Cloud Build", "Pub/Sub", "Datastream", "Dataflow", "Knowledge Catalog", "QuickSight", "Claude Code", "GitHub Copilot", "Cursor" ], "problemSolvingSkills" : "Data validation; Data testing; Data quality", "specialRequirements" : "Work from European Union region, Work permit required", "outcomesObjectives" : "Enable self-service analytics; Ensure KPI consistency", "qualificationsBasic" : "Analytics Engineer / Data Engineer experience, Hands-on dbt (or Dataform), SQL-based transformations experience, GCP stack experience, BigQuery experience, Cloud Storage experience, Composer/Airflow experience, SQL skills, Data models building experience, Dimensional modeling experience, Data marts experience, Modern data platforms experience, Lakehouse architectures experience, Data pipelines understanding, ETL/ELT processes understanding, Orchestration understanding, Airflow/Dagster or similar experience, Data validation experience, Data testing experience, Data quality frameworks experience, Stakeholder work experience, Business needs translation experience, Data migration projects familiarity, CI/CD for data experience, Terraform experience, GitHub Actions experience, Cloud Build experience, Data governance knowledge, Data cataloging knowledge, Data lineage tools knowledge, Streaming data processing exposure, Near real-time data processing exposure, AI/ML use cases familiarity, Analytics enablement use cases familiarity, AI-powered assistants practical experience, Work from European Union region, Work permit required", "qualificationsPreferred" : "Knowledge Catalog / data catalog tools experience, BI tools experience, QuickSight or similar experience, Self-service data platforms exposure, FinOps / cost optimization experience, Highly distributed enterprise environments experience", "remoteFriendly" : true, "rawDescription" : "Xebia is a global AI-first, digital transformation, and engineering partner. With over 25 years of experience and a team of 5,000 professionals across 16 countries, we help organizations design and build scalable products, platforms, and data-driven solutions. We specialize in Artificial Intelligence, Data and Cloud, Intelligent Automation, and Digital Products, combining deep technical expertise with a strong focus on engineering excellence and a people-first culture. In the CEE region, we’re a team of nearly 1,000 experts delivering modern applications, data platforms, and AI solutions for clients such as McLaren, Aviva, Deloitte, Spotify, Disney, ING, UPS, Tesco, Truecaller, AllSaints, Volotea, Schmitz Cargobull, Allegro, InPost, and many, many more. We work with leading technologies including AWS, Azure, GCP, Databricks, and Snowflake, and combine strong engineering culture with a consulting mindset and a continuous focus on growth and knowledge sharing. You will be: designing, building and maintaining data models (mainly in dbt/Dataform) on top of BigQuery, developing and optimizing analytical datasets and data marts for business consumption, collaborating with data engineers and business stakeholders to translate requirements into scalable data solutions, implementing data transformation logic and ensure data quality, testing, and validation, supporting migration of existing pipelines from AWS / Snowflake / Azure into GCP, working with ingestion pipelines (Pub/Sub, Datastream, Dataflow) and ensure alignment with downstream reporting needs, contributing to governance, data cataloging, and lineage (Knowledge Catalog), enabling self-service analytics through reusable models, templates, and standards, validating data consistency during migration and support cutover (parity vs legacy systems), supporting BI layer (e. g. QuickSight) and ensure consistency of KPIs across domains, participating in establishing best practices for analytics engineering and data product development. Your profile: strong experience as Analytics Engineer / Data Engineer with focus on analytics layer, hands-on experience with dbt (or Dataform) and SQL-based transformations, experience with GCP stack (BigQuery, Cloud Storage, Composer/Airflow), strong SQL skills and experience building data models (dimensional modeling, data marts), experience working with modern data platforms / lakehouse architectures, understanding of data pipelines, ETL/ELT processes, and orchestration (Airflow/Dagster or similar), experience with data validation, testing, and data quality frameworks, ability to work with stakeholders and translate business needs into data models, familiarity with data migration projects (replatforming, consolidation), experience with CI/CD for data (e.g., Terraform, GitHub Actions, Cloud Build), knowledge of data governance, cataloging and lineage tools, exposure to streaming or near real-time data processing, familiarity with AI/ML or analytics enablement use cases, practical experience using AI-powered assistants (e. g. Claude Code, GitHub Copilot, Cursor) to improve productivity, quality, or decision-making in software delivery. Work from the European Union region and a work permit are required. Nice to have: experience with Knowledge Catalog / data catalog tools Experience with BI tools (e.g., QuickSight or similar), exposure to self-service data platforms, understanding of FinOps / cost optimization in cloud data platforms, experience in highly distributed enterprise environments. Recruitment Process: CV review – HR call – Technical Interview – Client Interview – Decision", "summaryDescription" : "Senior Analytics Engineer (GCP) at Xebia. Skills: Analytics Engineering, GCP, BigQuery, Dbt. Design data models. 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Our AI-driven, codeless, and continuous testing platform empowers enterprises to accelerate innovation, deliver higher-quality releases, and transform digital velocity at scale. Recognized as a global leader by Gartner, Forrester, and IDC, Tricentis partners with the world’s largest and most innovative companies. We’re a team of curious learners, ambitious achievers, and collaborative competitors who believe in constant growth—both for our customers and ourselves. If you’re motivated by challenge, feedback, and the pursuit of excellence, you’ll thrive here. ## About the Role We’re looking for an accomplished and strategic Account Director to join the Tricentis Enterprise Federal Sales team. In this role, you’ll lead high-value sales cycles with some of the world’s largest organizations, building long-term, trusted relationships with senior executives and driving transformational business outcomes through Tricentis’ testing and automation solutions. You’ll bring deep enterprise sales expertise, a strong grasp of forecasting and pipeline discipline, and the leadership presence to influence at the C-suite level. This is an exciting opportunity for a seasoned sales professional who thrives on complexity, strategy, and delivering measurable impact. ## ## What You’ll Do * Own and expand strategic enterprise accounts — identifying opportunities, building exec relationships, and closing complex multi-stakeholder deals. * Develop deep understanding of Tricentis' products and how they drive business value * Engage with C-level and senior IT leaders, understanding their business drivers and aligning software solutions to their strategic goals * Deliver accurate forecasting and pipeline management with consistent achievement of revenue goals. * Partner with Pre-Sales, Customer Growth, and Marketing to maximize account strategy and long-term success. ## Qualifications _Must Have:_ * 8+ years experience selling enterprise B2B SaaS solutions to senior IT personas at large enterprises * Proven record of exceeding quotas and managing long, complex sales cycles with multiple stakeholders. Experience closing transactions >$500k ACV. _Nice to Have:_ * Knowledge of and/or experience with Tricentis products * Quality/testing industry experience ## Skills You Bring * Ownership and expansion of strategic enterprise accounts — identifying opportunities, building exec relationships, and closing complex multi-stakeholder deals. * Experience in forecasting and pipeline management discipline, with a data-driven approach to revenue predictability and execution * Engaging with C-level and senior IT leaders, understanding their business drivers and aligning software solutions to their strategic goals * Ability to translate technical customer challenges into negative business impact & map Tricentis solutions to quantifiable positive business outcomes * Cross-functional partnership with Pre-Sales, Customer Growth, and Marketing to drive account strategy, maximize customer value, and ensure long-term success. * Demonstrable experience and appreciation with MEDDPICC & value-selling * Experience with CRM & sales enablement tools (e.g., Salesforce, Clari, Outreach) * Experience using AI tools (e.g., Claude Chat/Co-Work/Code) ## Who You Are * Coachable: You show self-awareness and growth mindset by seeking feedback and continually refining your approach. * Gritty: You persevere through challenges, adapt quickly, and maintain focus and motivation under pressure. * Driven for Results: You set ambitious goals, take ownership of outcomes, and balance both tactical precision and strategic execution. * Scrappy: You’re resourceful, creative, and find ways to win — no matter the constraints, challenging the status quo, while thinking holistically about scale and impact. * Collaborative: You thrive in a team environment and celebrate shared success, solving problems in collaboration with others that benefit both us and our customers. ## Tricentis Core Values: At Tricentis, we strive for success while inspiring those around us by knowing what we need to achieve and how we’ll achieve it. Our core values serve as our guiding light to drive our every action and define our ways of working so that we can create and enjoy a successful journey and reach higher heights together. * Demonstrate Self-Awareness: Own your strengths and limitations. * Finish What We Start: Do what we say we are going to do. * Move Fast: Create momentum and efficiency. * Run Towards Change: Challenge the status quo. * Serve Our Customers & Communities: Create a positive experience with each interaction. * Solve Problems Together: We win or lose as one team. * Think Big & Believe: Set extraordinary goals and believe you can achieve them. ## We offer: * Competitive market salary + success-oriented commission / bonus * Supportive and engaged leadership team. * Career path and professional & personal development. * 401(k) / pension plan and full benefits package available. * Enhanced statutory Maternity and Paternity Pay * Personal and professional development. * A number of leave offerings: volunteer days, vacation days, public holidays, and flex/floating leave days. * And more! Tricentis is proud to be an equal opportunity workplace. Qualified applicants will receive consideration for employment without regard to race, color, ethnicity, gender, religious affiliation, age, sexual orientation, socioeconomic status, or physical and mental disability and other statuses protected by law. **_Global Sanctions Compliance _** We comply with all applicable global sanctions and export control laws. Candidates must not be listed on any government restricted party lists (including OFAC SDN List and U.S. Commerce Department restricted lists) and must certify that their employment would not violate any sanctions or export control regulations. Candidates must notify us of any changes to their status during the application process or subsequent employment. **_U.S. Work Authorization:_** This role is not eligible for employer-sponsored work visas. 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C. Pay Range: $160,000 - $180,000 USD LightFeather is seeking a GCP Cloud/DevOps Engineer who will play a critical role in designing, implementing, and maintaining cloud infrastructure solutions within Google Cloud Platform (GCP). This role requires expertise in infrastructure automation, cloud security, networking, and CI/CD pipeline development. The ideal candidate will work closely with cross-functional teams to drive cloud optimization and automation efforts in a high-security government environment. This role offers an exciting opportunity to shape cloud automation and infrastructure strategies in a high-impact government environment. Location: In-Person (5 days/week) in Washington, DC Job Type: Full Time Clearance Requirement: U. S. citizenship is required for this position due to federal contract requirements and the need to obtain and maintain a Top Secret-level security clearance Key Responsibilities Design, implement, and manage secure and scalable cloud infrastructure using GCP. Develop and maintain infrastructure-as-code (IaC) using Terraform, Deployment Manager, or similar tools. Support CI/CD pipeline automation, integration, and management. Collaborate with software engineers, security personnel, and government stakeholders to support development and deployment workflows. Monitor system performance, troubleshoot issues, and ensure cloud services meet SLAs. Implement cloud best practices and ensure compliance with federal security standards (e.g., FedRAMP, NIST). Provide documentation and knowledge sharing with the broader engineering team. Required Qualifications Willing to obtain a security clearance. 4+ years of experience in cloud engineering, with at least 2 years on GCP. Hands-on experience with GCP services such as Compute Engine, Cloud Functions, VPC, IAM, GKE, and BigQuery. Experience with infrastructure-as-code tools like Terraform, Ansible, or Deployment Manager. Familiarity with CI/CD tools such as GitLab CI, Jenkins, or Cloud Build. Solid understanding of Linux systems, networking, and containerization (Docker, Kubernetes). Experience working in an Agile/Scrum environment. Preferred Skills GCP Professional Cloud Architect or DevOps Engineer certification. Experience supporting federal government contracts and understanding of ATO processes. Familiarity with other cloud platforms (AWS, Azure) is a plus. Scripting skills in Python, Bash, or Go. Why Join LightFeather? At LightFeather, you're not just taking a job—you’re joining a purpose-driven team that delivers innovative, mission-critical solutions to make a real difference. You’ll work on diverse, meaningful projects that challenge and inspire you, alongside some of the best minds in the industry. LightFeather is an Equal Opportunity Employer. We consider all qualified applicants for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, disability, veteran status, genetic information, or any other status protected by applicable federal, state, or local law.", "summaryDescription" : "GCP Cloud/DevOps Engineer at LIGHTFEATHER IO LLC. Skills: GCP, DevOps, Cloud Engineering, Infrastructure as Code. Design and implement cloud infrastructure. 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A vehicle dating back to 1960. One that forged the path for future generations of rugged SUVs and trucks and will do so once again. But Scout is more than just a brand, it’s a legacy steeped in a culture of exploration, caretaking, and hard work. The Scout brand is all about respect. Respect for the past and the future by taking an iconic American brand that hasn’t been around for a while, electrifying it, digitizing it, and loading it with American innovation. Respect for communities by creating a company that stands for its people and its customers. Respect for both work and play, with vehicles that are equally at home at a camp site, a job site, or on a Tuesday commute. And respect for our customers by developing two powertrains that meet their requirements — an all-electric powertrain as well as the Harvester™ range extender powertrain which includes a built-in gas-powered generator with an estimated 500 miles of combined range. At Scout Motors, we empower our talented, inclusive, and entrepreneurial teams to innovate. What makes a Scout employee? Someone who is a visionary and a leader, who seeks new paths and shares lessons learned. A knowledgeable doer who collaborates across the company to build better. A go-getter with unrivaled passion. Join us at Scout Motors and be part of shaping the future of transportation. If you're ready to drive change and make history, apply now! What you’ll do Become part of an iconic brand that is set to revolutionize the electric pick-up truck advanced degree preferred. 15+ years of progressive growth and leadership experience within manufacturing, industrial, automotive, or similarly complex operational environments. Demonstrated success leading multiple business functions and teams. Proven ability to lead through organizational growth, operational ramp-up, startup environments, or significant business transformation. Experience leading within matrixed organizations, balancing local operational needs with enterprise standards and priorities. Strong business acumen, financial management, and organizational leadership skills, including experience managing budgets, resources, and performance objectives. Ability to build credibility and influence across all levels of an organization, from frontline employees to senior executives. Working knowledge of manufacturing-related regulatory and compliance frameworks. Ability and willingness to travel domestically and internationally as required Valid driver's license required. Passport required What you'll gain The benefits of joining Scout include the chance to build products and a company from the ground up. This is a chance to create something new and lasting – with an iconic brand at its foundation. In addition, Scout provides competitive compensation and benefits to support your physical, mental, and financial wellbeing. Program specifics are detailed in company policies and employee benefit guides, select highlights: Competitive insurance including: Medical, dental, vision and income protection plans 401(k) program with: An employer match and immediate vesting Generous Paid Time Off including: 20 days planned PTO, as accrued 40 hours of unplanned PTO and 14 company or floating holidays, annually Up to 16 weeks of paid parental leave for biological and adoptive parents of all genders Paid leave for circumstances related to bereavement, jury duty, voting time, or military leave Corporate Vehicle Program with: Eligibility for 1 assigned vehicle A mobility stipend Pay Transparency This is a full-time, exempt position eligible to receive a base salary and to participate in an annual performance bonus program. Final salary offered will be determined based on factors including but not limited to the candidate's skills and experience. The annual performance bonus program is preset and not candidate dependent. Initial base salary range = $210,000.00 - $255,000.00 Internal leveling code: M5 Notice to applicants: To be considered for career opportunities at Scout Motors, applicants must be 18 years of age or older. Residing in San Francisco: Pursuant to the San Francisco Fair Chance Ordinance, Scout Motors will consider for employment qualified applicants with arrest and conviction records. Residing in Los Angeles: Scout Motors will consider for employment qualified applicants with criminal histories in a manner consistent with the Los Angeles Fair Chance Initiative for Hiring Ordinance. Residing in New York City: This role is not eligible for remote work in New York City. Equal Opportunity Scout Motors is committed to employing a diverse workforce and is proud to be an Equal Opportunity Employer. Qualified applicants will receive consideration without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, gender expression, veteran status, disability, pregnancy, or any other characteristics protected by law. Scout Motors is committed to compliance with all applicable fair employment practice laws. If you require reasonable accommodation to complete a job application, pre-employment testing, or a job interview or to otherwise participate in the hiring process, please contact ScoutAccommodations@scoutmotors.com.", "summaryDescription" : "Senior Director, Administration at Scout Motors", "postedDate" : "2026-06-15T23:20:07.862", "createdAt" : "2026-06-15T23:20:07.862", "lastUpdated" : "2026-06-16T10:02:34.736", "ingestTimestamp" : "2026-06-15T23:20:07.862", "mongoId" : "6a305198f292fd229cf02edc", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 210000, "salaryAnnualMax" : 255000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 718.32745, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Automotive", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c622f74d8ee00a08f62bf", "title" : "Director, Quality Control & Quality Assurance", "company" : "Vorbeck", "industry" : "Research", "salary" : { "min" : 100000.0, "max" : 125000.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "Grand Forks, ND, United States", "locations" : [ "Grand Forks", "ND", "United States" ], "timestamp" : "2026-06-15T03:42:17.939", "fingerprint" : "0af57124bb1c6902b962753a407947d65180e2354eed2c6a79b500e92d35b310", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/Vorbeck/744000131733429-director-quality-control-quality-assurance", "externalId" : "744000131733429", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Grand Forks", "state" : "North Dakota", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "47.9252104,-97.0306325" } ], "locationText" : "Grand Forks, North Dakota, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 10, "experienceMaxYears" : 15, "experienceLevel" : "director", "professionalSkills" : [ "Quality systems management", "Product testing", "Quality assurance", "Compliance initiatives", "Operational excellence", "Risk management", "Safety culture" ], "hardSkillsList" : [ "Quality control methodologies", "Continuous improvement principles", "Laboratory testing methods", "Quality data analysis", "Root cause investigations", "Corrective action implementation" ], "softSkillsList" : [ "Leadership", "Mentoring" ], "hardSkills" : [ { "name" : "Quality control methodologies", "level" : "intermediate" }, { "name" : "Continuous improvement principles", "level" : "intermediate" }, { "name" : "Laboratory testing methods", "level" : "intermediate" }, { "name" : "Quality data analysis", "level" : "intermediate" }, { "name" : "Root cause investigations", "level" : "intermediate" }, { "name" : "Corrective action implementation", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "Quality control, Quality assurance, Team leadership", "majorSkillsList" : [ "Quality control", "Quality assurance", "Team leadership" ], "coreResponsibilities" : "Maintain quality management systems, Refine quality management systems, Improve quality management systems, Oversee product testing, Oversee inspection activities, Analyze testing data, Identify testing trends, Investigate quality issues, Implement corrective actions, Ensure compliance with standards, Lead internal audits, Support quality reviews, Manage documentation control, Lead continuous improvement initiatives, Lead and mentor personnel, Provide training and guidance, Provide performance feedback, Partner with Production, Partner with R&D, Partner with Engineering, Partner with Operations, Address quality concerns, Support process improvements, Ensure implementation of changes, Drive initiatives to improve quality, Drive initiatives to improve testing efficiency, Drive initiatives to improve manufacturing consistency, Drive initiatives to improve operational performance, Promote safety culture, Identify potential hazards, Conduct risk assessments, Ensure quality activities compliance, Support additional projects", "teamCollaboration" : "Cross-functional teams; Production teams; R&D teams; Engineering teams; Operations teams", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Chemical manufacturing; Materials manufacturing; Specialty chemicals; Coatings; Industrial products; Quality management systems; Quality control methodologies; Continuous improvement principles; Environmental standards; Health standards; Safety standards; Operational requirements", "domainList" : [ "chemical-manufacturing", "materials-manufacturing", "specialty-chemicals", "coatings", "industrial-products", "quality-management-systems", "quality-control-methodologies", "continuous-improvement-principles", "environmental-standards", "health-standards", "safety-standards", "operational-requirements" ], "domainSpecificKnowledge" : [ "Chemical manufacturing", "Materials manufacturing", "Specialty chemicals", "Coatings", "Industrial products", "Quality management systems", "Quality control methodologies", "Continuous improvement principles", "Environmental standards", "Health standards", "Safety standards", "Operational requirements" ], "communicationSkills" : "Verbal communication; Written communication", "documentationSkills" : "Quality procedures; Specifications; Test methods; Quality reports; Technical documentation", "problemSolvingSkills" : "Troubleshooting; Problem-solving skills; Root cause investigations", "specialRequirements" : "10% travel, United States citizens, Walk, stand, stoop, bend, kneel, climb, Lift and carry up to 25 pounds", "outcomesObjectives" : "Ensure product consistency; Ensure process reliability; Maintain product quality; Maintain operational excellence; Improve manufacturing performance", "qualificationsBasic" : "Bachelor's degree in technical field required, 5+ years quality assurance experience, 2+ years leadership experience", "qualificationsPreferred" : "Master's degree or Ph. D. preferred, Experience in chemical manufacturing preferred, Experience supporting audits preferred, Experience managing quality documentation preferred", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Vorbeck Materials is engineering the future of technology for first responders, military, and industry. From PFAS-free firefighting foams to conformal antennas, we deliver mission-critical solutions with superior performance. Job Type: Full-time Classification: Exempt Pay: $100,000 - $125,000, based on qualifications and experience Physical Setting/work location: Onsite, Grand Forks, ND. Vorbeck is seeking a Director of Quality Control & Quality Assurance to lead quality operations across our manufacturing and testing environments. This role is responsible for maintaining and continuously improving established quality systems, overseeing product testing and inspection activities, supporting compliance initiatives, and partnering with cross-functional teams to ensure consistent product quality and operational excellence. * Quality Systems Management: Maintain, refine, and continuously improve quality management systems, procedures, and documentation to ensure product consistency, process reliability, and compliance with internal and external standards. * Quality Control & Testing: Oversee product testing and inspection activities to ensure materials meet established specifications and performance requirements. Analyze testing data, identify trends, investigate quality issues, and implement corrective actions as needed. * Quality Assurance & Compliance: Ensure compliance with company quality standards, customer requirements, regulatory requirements, and applicable industry standards. Lead and support internal audits, quality reviews, documentation control activities, and continuous improvement initiatives to maintain product quality and operational excellence. * Team Leadership: Lead and mentor laboratory technicians and quality personnel, providing training, guidance, and performance feedback to promote a culture of quality, accountability, and continuous improvement. * Cross-Functional Collaboration: Partner with Production, R&D, Engineering, and Operations teams to address quality concerns, support process improvements, and ensure successful implementation of product and process changes. * Continuous Improvement: Drive initiatives to improve product quality, testing efficiency, manufacturing consistency, and overall operational performance through data analysis, root cause investigations, and corrective action implementation. * Risk Management, Safety & Compliance: Promote a strong safety culture by identifying potential hazards, conducting risk assessments, and ensuring quality activities are performed in accordance with environmental, health, safety, and operational requirements. * Other Responsibilities: Support additional projects and initiatives as assigned. * Travel (expected): 10% ## Qualifications Education * Bachelor's degree in Chemical Engineering, Chemistry, Materials Science, or a related technical field required. Master's degree or Ph.D. preferred. Experience * 5+ years of experience in quality assurance, quality control, or manufacturing quality within a technical or manufacturing environment. * 2+ years of leadership experience managing quality personnel, laboratory staff, or cross- functional quality initiatives. * Experience working within chemical manufacturing, materials manufacturing, specialty chemicals, coatings, industrial products, or related technical industries preferred. * Experience developing, implementing, maintaining, and improving quality systems, procedures, and documentation. * Experience leading root cause investigations, corrective actions, and continuous improvement initiatives. * Experience analyzing quality data and utilizing results to drive process and product improvements. * Proven success collaborating with Production, Engineering, Operations, and R&D teams to resolve quality issues and improve manufacturing performance. * Experience supporting audits, compliance activities, and quality documentation management preferred. Skills and Abilities * Exceptional drive and work ethic. * Strong leadership and team development skills, with the ability to mentor and support quality and laboratory personnel. * Strong understanding of quality management systems, quality control methodologies, and continuous improvement principles. * Excellent analytical, troubleshooting, and problem-solving skills. * Experience with laboratory testing methods, quality data analysis, and interpretation of test results. * Skilled in technical documentation, including quality procedures, specifications, test methods, and quality reports. * Strong organizational and project management skills, with the ability to manage multiple priorities in a fast-paced environment. * Effective verbal and written communication skills with the ability to work collaboratively across departments. * Knowledge of applicable quality, safety, and environmental standards and regulations. Physical Requirements * Must be able to walk, stand, stoop, bend, kneel, and climb stairs/ladders regularly. * Ability to lift and carry up to 25 pounds regularly as part of daily responsibilities. ## Additional Information Benefits include: * Medical, Dental, and Vision Insurance * 401(k) Program * Vacation, Personal Time, and 10 Paid Holidays * Company-sponsored Short-Term Disability, Long-Term Disability, and Life Insurance * Opportunity for Relocation Assistance Vorbeck is an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, ethnicity, national origin, religion, sex (including pregnancy, childbirth, lactation, or related medical conditions), marital status, sexual orientation, gender identity and expression, disability, veteran status, military or uniformed service member status, or any other status protected by applicable federal, state, local, or international law. This position will involve work on government contracts and the government requires that qualified candidates must be United States citizens. All personal information will be kept confidential according to EEO guidelines.", "summaryDescription" : "Director, Quality Control & Quality Assurance at Vorbeck. Skills: Quality control, Quality assurance, Team leadership. Maintain quality management systems. Refine quality management systems", "postedDate" : "2026-06-11T17:39:39.000", "createdAt" : "2026-06-13T12:08:26.881", "lastUpdated" : "2026-06-15T03:42:17.939", "ingestTimestamp" : "2026-06-13T12:08:26.881", "mongoId" : "6a2c622f74d8ee00a08f62bf", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 100000, "salaryAnnualMax" : 125000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Quality control methodologies", "Continuous improvement principles", "Laboratory testing methods", "Quality data analysis", "Root cause investigations", "Corrective action implementation", "Leadership", "Mentoring", "Quality control", "Quality assurance", "Team leadership", "Quality systems management", "Product testing", "Compliance initiatives", "Operational excellence", "Risk management", "Safety culture", "Project management", "Chemical manufacturing", "Materials manufacturing", "Specialty chemicals", "Coatings", "Industrial products", "Quality management systems", "Environmental standards", "Health standards", "Safety standards", "Operational requirements" ], "skillCount" : 28, "jobCategory" : "other", "jobSubcategory" : "quality-assurance", "dataQualityScore" : 1.0, "_score" : 717.6592, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a2c6ad774d8ee00a090e6e8", "title" : "Senior Quality Assurance Test Expert", "company" : "OMP Careers", "industry" : "Technology", "salary" : { "min" : 70000.0, "max" : 105000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on the market baseline for a Senior Quality Assurance Test Expert in Antwerp, Belgium, with adjustments for seniority and the technology industry." }, "location" : "BE-Antwerp", "locations" : [ "BE-Antwerp" ], "timestamp" : "2026-06-15T05:24:45.471", "fingerprint" : "ed2e6cb88de258be5ccd4de3337988fb16dedaef4e1d5c5418b618a091fc5f3c", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://careers.omp.com/job/navigate/4877163101?gh_jid=4877163101", "externalId" : "4877163101", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Antwerp", "country" : "Belgium", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "51.2211097,4.3997081" } ], "locationText" : "Antwerp, Belgium", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Web API, CI/CD", "majorSkills" : "Quality Assurance, Test Automation", "majorSkillsList" : [ "Quality Assurance", "Test Automation" ], "coreResponsibilities" : "Lead testing for projects, Design testing solutions, Define test environments setup, Guard automation framework setup, Apply expertise to challenges, Develop testing best practices, Develop delivery best practices, Develop educational materials, Inform senior management, Design manual test scenarios, Develop manual test scenarios, Follow up manual test scenarios, Execute manual test scenarios, Create CI/CD pipelines, Estimate testing priority, Estimate testing difficulty, Optimize test environments, Extend test environments, Track bugs, Document actions, Communicate with parties", "teamCollaboration" : "Software engineers; Project managers; Consultants", "documentationSkills" : "Documenting actions", "problemSolvingSkills" : "Complex testing challenges", "qualificationsBasic" : "Senior Quality Assurance Test Expert", "rawDescription" : "As a Senior Quality Assurance Test Expert, you lead the testing for medium and large development projects. You design optimal solutions for the high-quality testing of our technology, define and guard the overall setup of our test environments and automation framework, and apply your expertise to complex testing challenges. You are responsible for: Developing best practices for software testing, delivery, and educational materials. Informing senior management about long-range planning and challenges with respect to the quality of our solutions. Designing, developing, follow up and/or executing: Manual test scenarios. Automation scripts for web API, web-based UI, desktop applications, and continuous integration testing. Creating pipeline in CI/CD test automation Performance/load testing. Testing framework. Accurately estimating the priority level and difficulty of the required testing according to your plan. Continuously optimizing and extending our test environments. Tracking bugs and documenting your actions, while continuously communicating with all parties involved such as software engineers, project managers, and consultants.", "summaryDescription" : "Senior Quality Assurance Test Expert at OMP Careers. Skills: Quality Assurance, Test Automation. Lead testing for projects. Design testing solutions", "postedDate" : "2026-06-13T21:57:32.777", "createdAt" : "2026-06-13T21:57:32.777", "lastUpdated" : "2026-06-15T05:24:45.471", "ingestTimestamp" : "2026-06-13T21:57:32.777", "mongoId" : "6a2c6ad774d8ee00a090e6e8", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "50k-75k", "hasSalary" : false, "allSkills" : [ "Quality Assurance", "Test Automation" ], "skillCount" : 2, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 0.8888889, "_score" : 716.81604, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.95 }, { "id" : "6a30575ff292fd229cf38bd6", "title" : "[쿠팡] Quality Assurance Specialist (Andon Policy)", "company" : "Coupang", "industry" : "E-Commerce", "salary" : { "min" : 4.8E7, "max" : 6.5E7, "currency" : "KRW", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-seniority Quality Assurance Specialist in the E-commerce industry in Seoul, South Korea, adjusted for company size and specific role requirements." }, "location" : "Seoul, South Korea", "locations" : [ "Seoul", "South Korea" ], "timestamp" : "2026-06-16T09:24:00.243", "fingerprint" : "932919807d1c65ebd6857c3c8aa86bb832b7663b89283397ccaea6eda4bf76a1", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://boards.greenhouse.io/coupanginternal/jobs/8002532?gh_jid=8002532", "externalId" : "8002532", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Seoul", "country" : "South Korea", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "37.5666791,126.9782914" } ], "locationText" : "Seoul, South Korea", "employmentType" : "FULL_TIME", "experienceMinYears" : 3, "technicalSkills" : "Power Bi, Excel", "professionalSkills" : [ "Policy management", "Process management", "Data analysis", "Quality management", "Stakeholder management", "Decision making" ], "hardSkillsList" : [ "Data analysis", "Process improvement", "Policy development" ], "hardSkills" : [ { "name" : "Data analysis", "level" : "intermediate" }, { "name" : "Process improvement", "level" : "intermediate" }, { "name" : "Policy development", "level" : "intermediate" } ], "majorSkills" : "Andon policy, Quality assurance, Process management", "majorSkillsList" : [ "Andon policy", "Quality assurance", "Process management" ], "coreResponsibilities" : "Manage Andon non-food policies and common policies/processes, Operate Andon non-food policies and common policies/processes, Plan and reflect new Andon quality policies/processes, Provide customer-moving product experience, Communicate with various related departments, Develop policies/processes, Stabilize policies/processes, Set up and improve Andon common and non-food, Derive fundamental policy improvement plans through data analysis, Plan and manage proactive policies through collaboration with, Improve processes through periodic policy monitoring", "teamCollaboration" : "Related departments collaboration", "domainKnowledge" : "Andon policy; Non-food quality", "domainList" : [ "andon-policy", "non-food-quality" ], "domainSpecificKnowledge" : [ "Andon policy", "Non-food quality" ], "toolProficiency" : [ "Power Bi", "Excel" ], "problemSolvingSkills" : "Root cause analysis; Data analysis", "qualificationsBasic" : "3+ years policy and process establishment experience, Define root causes and identify business-impacting items from a macro perspective, Predict policy outcomes and impact, Proactively participate in customer experience improvement, Communicate effectively with various stakeholders and data", "qualificationsPreferred" : "Experience in non-food quality assurance, High proficiency in data analysis and work tools (Power Bi, Excel)", "workSiteFlexibility" : "Onsite", "rawDescription" : "반드시 첨부된 ‘사내공모지원서 양식’을 작성 후 제출하여 주시기 바랍니다. Please complete the attached Internal Transfer Request Form and submit. 반드시 쿠팡 이메일 계정으로 지원해 주시기 바랍니다. Please make sure to apply with your Coupang e-mail address. 회사 소개 쿠팡은 고객 감동 실현을 위해 존재합니다. 고객들이 \"쿠팡 없이 그동안 어떻게 살았을까?\" 라고 말할 때, 비로소 우리의 미션을 실현하고 있음을 알 수 있습니다. 고객들의 쇼핑과 식사, 생활 전반을 편하게 만들겠다는 유일한 집념으로 쿠팡은 수억 달러 규모의 커머스 산업 전반의 혁신을 이끌고 있습니다. 쿠팡은 가장 빠르게 성장하는 리테일 기업 중 하나로, 국내 커머스 업계에서의 독보적인 입지와, 고객 신뢰를 구축했습니다. 쿠팡은 스타트업 문화를 기반으로 한 글로벌 대형 상장사라고 자부합니다. 이것이 창립 당시의 기민함을 유지하며, 신규 서비스를 끊임없이 출시하며 비즈니스를 확장해 나가는 우리의 성장 동력입니다. 쿠팡의 모든 임직원에게는 기업가 정신을 갖추고 새로운 혁신과 이니셔티브를 추진할 수 있는 기회가 주어집니다. 주저없이 일에 뛰어들어 성과를 이루고자 하는 과감성이, 바로 쿠팡이 일하는 방식의 본질입니다. 쿠팡에서는 여러분 자신, 동료, 팀 그리고 회사 전체가 매일 성장하는 모습을 목격할 것입니다. 쿠팡의 모든 직원은 커머스의 미래를 만들겠다는 쿠팡의 미션에 진심입니다. 우리는 고객의 문제를 해결해 나가고, 전통적인 관념과 통념에 맞서며 실현가능한 한계를 뛰어넘고 있습니다. 고가용성(Always-on) 과 최첨단의 앞선 기술(High-tech), 초연결사회(Hyper-connected world) 에서의 놀라운 업무 경험을 원하신다면, 지금 바로 쿠팡에 합류하세요. 직무소개 쿠팡의 Andon 비식품 정책 담당자는 고객이 구매하고 사용하는 과정에서 발생되는 Andon의 비식품 정책 및 공통 정책/프로세스를 관리하고 운영합니다. 궁극적으로 고객을 감동시킬 수 있는 상품 경험을 제공하기 위해 새로운 Andon 품질 정책/프로세스를 기획하고 반영하며, 다양한 유관부서와의 커뮤니케이션을 통해 정책/프로세스를 더욱 발전시키고 안정화될 수 있도록 관리합니다. 업무 내용 • Andon 공통 및 비식품 정책 관련 시스템/프로세스 신규 셋업 및 개선 • 품질 관련 지표 및 VOC에 대한 데이터 분석을 통한 근본적인 정책 개선안 도출 • 유관부서와의 협력/품질동향 파악을 통한 선제적인 정책 기획 및 관리 • 주기적 정책 모니터링을 통한 프로세스 개선 자격 요건 • 고객 및 품질 관련 정책 및 프로세스 수립 업무 관련 경력을 3년 이상 보유하신 분 • 데이터 분석 및 모니터링을 통해 근본적인 문제를 정의하고, 거시적인 관점에서 안돈 및 비즈니스 전반에 영향을 주는 항목을 파악하여 정책/프로세스를 구축할 수 있는 분 • 다양한 이해관계 및 지표/유관부서의 니즈 등을 종합하여 정책에 따른 결과 및 영향도를 면밀하게 예측하여 올바른 의사결정을 내릴 수 있는 분 • 고객 경험 개선을 위해 주도적으로 참여하거나 진행한 경험이 있으신 분 • 다양한 유관부서와 데이터 기반의 원활한 커뮤니케이션을 하실 수 있는 분 우대 사항 • 비식품(가전, 생활, 이미용, 가구 등) 품질보증 업무 수행 경력이 있으신 분 • 데이터 분석 및 업무 툴(Power Bi, Excel 등) 활용 능력이 높으신 분 전형 절차 및 안내 사항 전형 절차 서류전형 - 폰 스크리닝 - 전화면접 - 대면(화상)면접 – 최종 합격 전형절차는 직무별로 다르게 운영될 수 있으며, 일정 및 상황에 따라 변동될 수 있습니다. 전형 일정 및 결과는 지원서에 등록하신 이메일로 개별 안내 드립니다. 참고 사항 본 공고는 모집 완료 시 조기 마감될 수 있습니다. 지원서 내용 중 허위사실이 있는 경우에는 합격이 취소될 수 있습니다. 취업 보호 대상자(보훈대상자, 장애인 등)는 관련 법률에 따라 채용우대를 받을 수 있습니다. 직급과 담당 업무 범위는 후보자의 전반적인 경력과 경험 등 제반사정을 고려하여 변경될 수 있습니다. 이러한 변경이 필요할 경우, 최종 합격 통지 전 적절한 시기에 후보자와 커뮤니케이션 될 예정입니다. 고용형태는 정규직으로 수습기간 12 주를 포함합니다. 단, 업무상 필요한 경우에는 상기 수습기간을 적용하지 않거나 단축 또는 연장할 수 있습니다. 채용 및 업무 수행과 관련하여 요구되는 법령상 자격이 갖추어지지 않은 경우 채용이 제한될 수 있습니다. 개인정보 처리방침  쿠팡 그룹은 입사지원자 개인정보 처리방침(아래 링크)에 따라 귀하의 개인정보를 수집하여 처리합니다. https://www.coupang.jobs/kr/privacy-policy  서류 반환 정책  본 고지는 『채용절차의공정화에관한법률』 제11조제6항에 따른 것 입니다. 당사 채용에 응시한 구직자 중 최종 합격이 되지 못한 구직자는 『채용절차의 공정화에 관한 법률』에 따라 제출한 채용서류의 반환을 청구할 수 있음을 알려 드립니다. 다만, 홈페이지 또는 전자우편으로 제출된 경우나 구직자가 당사의 요구 없이 자발적으로 제출한 경우에는 그러하지 아니하며, 천재지변이나 그 밖에 당사에게 책임 없는 사유로 채용서류가 멸실된 경우에는 반환한 것으로 봅니다. 위2항 본문에 따라 채용 서류 반환 청구를 하는 구직자는 채용 서류 반환 청구서 [채용절차의 공정화에 관한 법률 시행규칙 별지 제 3 호 서식]를 작성하여 이메일 (recruitingops@coupang.com) 로 제출하면, 제출이 확인된 날로부터 14 일 이내에 지정한 주소지로 등기우편을 통하여 발송해 드립니다. 이 경우 등기우편요금은 수신자 부담으로 하게 되오니 유념하시기 바랍니다.  당사는 위2항 본문에 따른 구직자의 반환 청구에 대비하여 채용 여부가 확정된 날로부터 180 일간 구직자가 제출한 채용서류 원본을 보관하게 되며, 그때까지 채용서류의 반환을 청구하지 아니할 경우에는 『개인정보 보호법』에 따라 지체 없이 채용서류 일체를 파기할 예정입니다. 단, 위 1항 내지 4항의 내용은 대한민국의 노동 관계 법령이 적용되는 경우에만 적용됩니다. 그 이외의 경우에는 적용되지 않습니다.", "summaryDescription" : "[쿠팡] Quality Assurance Specialist (Andon Policy) at Coupang. Skills: Andon policy, Quality assurance, Process management. Manage Andon non-food policies and common policies/processes. Operate Andon non-food policies and common policies/processes", "postedDate" : "2026-06-15T23:24:14.533", "createdAt" : "2026-06-15T23:24:14.533", "lastUpdated" : "2026-06-16T09:24:00.243", "ingestTimestamp" : "2026-06-15T23:24:14.533", "mongoId" : "6a30575ff292fd229cf38bd6", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Data analysis", "Process improvement", "Policy development", "Andon policy", "Quality assurance", "Process management", "Policy management", "Quality management", "Stakeholder management", "Decision making", "Non-food quality", "Power Bi", "Excel" ], "skillCount" : 13, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.8888889, "_score" : 713.1707, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "E-Commerce", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2ca0f974d8ee00a09a3f55", "title" : "Senior Quality Assurance Engineer L4", "company" : "Inovalon", "industry" : "3806 - Software Engineering COR", "salary" : { "min" : 125000.0, "max" : 175000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on 2024-2025 market data for a Senior Quality Assurance Engineer L4 in Canonsburg, United States, with adjustments for seniority, company size, and the healthcare industry." }, "location" : "Office: Canonsburg", "locations" : [ "Office: Canonsburg" ], "timestamp" : "2026-06-15T07:21:05.364", "fingerprint" : "433cf885c8e493c33f70ce221f418166555591700ff4e817df9a6798aa0302c0", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/inovalon/1d42fa75-26ee-4d9c-8dbe-04f0340cc11c/application", "externalId" : "1d42fa75-26ee-4d9c-8dbe-04f0340cc11c", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Canonsburg", "state" : "Pennsylvania", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.2588173,-80.1867206" } ], "locationText" : "Canonsburg, Pennsylvania, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Cloud-native, UI testing, API testing, Data layer testing, Programming languages, Software testing tools", "professionalSkills" : [ "Technical testing", "Analytical skills", "SQA concepts", "SQA methods", "Quality measurement" ], "hardSkillsList" : [ "Performance testing", "Load testing", "Regression testing", "System testing", "Functional testing", "Interface testing", "Database testing", "Positive testing", "Negative testing" ], "hardSkills" : [ { "name" : "Performance testing", "level" : "intermediate" }, { "name" : "Load testing", "level" : "intermediate" }, { "name" : "Regression testing", "level" : "intermediate" }, { "name" : "System testing", "level" : "intermediate" }, { "name" : "Functional testing", "level" : "intermediate" }, { "name" : "Interface testing", "level" : "intermediate" }, { "name" : "Database testing", "level" : "intermediate" }, { "name" : "Positive testing", "level" : "intermediate" }, { "name" : "Negative testing", "level" : "intermediate" } ], "majorSkills" : "Quality Assurance, Test Automation, Agile Scrum", "majorSkillsList" : [ "Quality Assurance", "Test Automation", "Agile Scrum" ], "coreResponsibilities" : "Execute test scripts, Create test plans, Create test cases, Design automation-ready tests, Use AI-assisted tools, Troubleshoot with developers, Perform performance testing, Perform load testing, Analyze test results, Report test results, Organize tasks, Execute workload, Analyze requirements, Analyze specifications, Define test plans, Develop test scripts, Maintain test scripts, Develop test cases, Maintain test cases, Develop test tools, Maintain test tools, Identify complex issues, Isolate complex issues, Maintain compliance, Adhere to policies, Fulfill responsibilities", "teamCollaboration" : "Agile Scrum team; Work with developers", "projectManagementSkills" : [ "Agile", "Scrum" ], "domainKnowledge" : "Healthcare Informatics; Cloud-native application", "domainList" : [ "healthcare-informatics", "cloud-native-application" ], "domainSpecificKnowledge" : [ "Healthcare Informatics", "Cloud-native application" ], "toolProficiency" : [ "AI-assisted tools", "Microsoft Azure DevOps", "GitHub" ], "communicationSkills" : "Communicate effectively", "documentationSkills" : "Test plan documentation; Test case documentation", "problemSolvingSkills" : "Troubleshoot; Analyze gaps; Identify deficiencies; Analyze test results; Identify complex issues", "specialRequirements" : "Sedentary work, Less than 5% travel, Not eligible for immigration sponsorship, Authorized to work in US", "qualificationsBasic" : "5+ years QA experience, Test case development, Basic test techniques, Basic test phases, Software development life cycle, Agile software development, Effective team lead, Communicate effectively, Source control tools", "qualificationsPreferred" : "Automated test experience desirable, Understanding of automated testing", "rawDescription" : "Overview: We are seeking a Senior Quality Engineer with a strong technical foundation to join an Agile Scrum team responsible for delivering and sustaining a large, cloud‑native application. This role goes beyond traditional manual QA execution and requires someone who can think technically, work closely with Software Engineers, and design tests with automation in mind from the start. As a Senior Quality Engineer, you will participate fully in Agile Scrum ceremonies, contribute to sprint planning and backlog refinement, and ensure that quality is built into features early. You will leverage AI‑assisted tools, technical testing techniques, and strong analytical skills to create effective test coverage across UI, API, and data layers. We promote an upbeat and effective team environment within the fast-growing IT Healthcare Informatics industry. Duties and Responsibilities: - Execute test scripts for complex and broadly used product capabilities and components; - Create and maintain comprehensive test plans and test cases for user stories, defects, and technical enhancements. - Design test cases that are automation‑ready, clearly structured, and reusable by Quality Engineers and automated test frameworks. - Use AI‑assisted tools to accelerate test case creation, expand test coverage, identify edge cases, and improve test effectiveness (with human judgment applied to validation and refinement). - Work with developers to help troubleshoot defects; - Set up, perform, and understand performance and load tests; - Identify, analyze, and communicate issues; - Demonstrate knowledge, proficiency, and practical application of SQA concepts, methods, and tools; - Identify gaps and deficiencies in existing test plans, scripts, and cases, and effectively extend test plans where necessary; - Analyze and report test results and testing status from an overall product perspective; - Organize and execute tasks and overall workload based on team goals and priorities; - Demonstrate an understanding of all facets of software product testing and quality measurement, including awareness of generally available and accepted solutions that apply to each facet; - Analyze functional requirements and specifications and based on this analysis, (1) identify gaps in the defined requirements and specifications and (2) define a test plan that will assure that the defined requirements and specifications are fully met; - Develop and maintain test scripts and cases, and software test and performance measurement tools using appropriate programming languages or software applications; and - Responsible for identifying and isolating complex issues related to the interaction and usage of dependent parts of software. - Maintain compliance with Inovalon’s policies, procedures and mission statement; - Adhere to all confidentiality and HIPAA requirements as outlined within Inovalon’s Operating Policies and Procedures in all ways and at all times with respect to any aspect of the data handled or services rendered in the undertaking of the position; - Fulfill those responsibilities and/or duties that may be reasonably provided by Inovalon for the purpose of achieving operational and financial success of the Company; - Uphold responsibilities relative to the separation of duties for applicable processes and procedures within your job function; and - We reserve the right to change this job description from time to time as business needs dictate and will provide notice of such. Job Requirements: - 5+ years of demonstrated QA and testing experience or equivalent experience; - Test case development experience; - Good knowledge of basic test techniques (positive/negative testing, interface testing, database testing); - Basic knowledge of test phases (integration/functional, regression, system); - Test tool experience; - Automated test experience is desirable and understanding of databases; - Experience in validating effectiveness of user experience of application; - Thorough understanding of basic software development life cycle and the concept of quality before design (QA isn’t just test execution) Agile software development experience; - Effective team lead and the ability to communicate effectively within a variety of staff levels; and - Experience using source control tools – Microsoft Azure DevOps, and/or GitHub. Education: - Bachelor’s degree in Computer Science or Information Technology. Physical Demands and Work Environment: - Sedentary work (i.e., sitting for long periods of time); - Exerting up to 10 pounds of force occasionally and/or negligible amount of force; - Frequently or constantly to lift, carry push, pull or otherwise move objects and repetitive motions; - Subject to inside environmental conditions; and - Travel for this position will include less than 5% locally usually for training purposes. This position is not eligible for immigration sponsorship (e.g. H-1B, TN, or E-3). Applicants must be authorized to work in the United States as a condition of employment. (This is only applicable for US-based positions) If you don’t meet every qualification listed but are excited about our mission and the work described, we encourage you to apply. Inovalon is most interested in finding the best candidate for the job, and you may be just the right person for this or other roles. By embracing inclusion, we enhance our work environment and drive business success. Inovalon strives to provide equal opportunities to the communities where we operate and to our clients and everyone whom we serve. We endeavor to create a culture of inclusion in which our associates feel empowered to bring their full, authentic selves to work and pursue their professional goals in an equitable setting. We understand that by fostering this type of culture, and welcoming different perspectives, we generate innovation and growth. Inovalon is proud to be an equal opportunity workplace. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirement. To review the legal requirements, including all labor law posters, please visit this link https://postings.govdocs.com/#/8sZXnFNWk3KYs3F To review the California Consumer Privacy Statement: Disclosures for California Residents, please visit this link https://www.inovalon.com/privacy-policy/", "summaryDescription" : "Senior Quality Assurance Engineer L4 at Inovalon. Skills: Quality Assurance, Test Automation, Agile Scrum. Execute test scripts. Create test plans", "createdAt" : "2026-06-14T06:41:40.303", "lastUpdated" : "2026-06-15T07:21:05.364", "ingestTimestamp" : "2026-06-14T06:41:40.303", "mongoId" : "6a2ca0f974d8ee00a09a3f55", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 125000, "salaryAnnualMax" : 175000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Performance testing", "Load testing", "Regression testing", "System testing", "Functional testing", "Interface testing", "Database testing", "Positive testing", "Negative testing", "Quality Assurance", "Test Automation", "Agile Scrum", "Technical testing", "Analytical skills", "SQA concepts", "SQA methods", "Quality measurement", "Agile", "Scrum", "Healthcare Informatics", "Cloud-native application", "AI-assisted tools", "Microsoft Azure DevOps", "GitHub" ], "skillCount" : 24, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 0.8888889, "_score" : 710.0367, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 } ], "status" : 200, "message" : "OK", "pagination" : { "page" : 0, "limit" : 50, "totalCount" : 123422, "totalPages" : 2469, "hasNext" : true, "hasPrevious" : false } }

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