{ "count" : 77092, "data" : [ { "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. 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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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Healthcare industry." }, "location" : "Tokyo, Tokyo, JP", "locations" : [ "Tokyo", "Tokyo", "JP" ], "timestamp" : "2026-06-16T10:57:59.794", "fingerprint" : "c6ab4a9384305a665d06d0e4b2af5fa16de4a7d820fa8fca2f2ec84fbaef0a70", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/PSICRO/744000132166364-quality-assurance-auditor", "externalId" : "744000132166364", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Tokyo", "state" : "Tokyo", "country" : "Japan", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "35.6812546,139.7667060" } ], "locationText" : "Tokyo, Tokyo, Japan", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "technicalSkills" : "MS Office", "professionalSkills" : [ "Quality management", "Quality assurance", "Study audits", "Vendor qualification", "Internal systems audits", "Process audits" ], "hardSkillsList" : [ "QA study audits", "Internal systems audits", "Internal locations audits", "Vendor qualification audits", "Internal process audits" ], "softSkillsList" : [ "Presentation skills", "Customer-service skills", "Team building skills", "Leadership skills", "Organizational skills" ], "hardSkills" : [ { "name" : "QA study audits", "level" : "intermediate" }, { "name" : "Internal systems audits", "level" : "intermediate" }, { "name" : "Internal locations audits", "level" : "intermediate" }, { "name" : "Vendor qualification audits", "level" : "intermediate" }, { "name" : "Internal process audits", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Presentation skills" }, { "name" : "Customer-service skills" }, { "name" : "Team building skills" }, { "name" : "Leadership skills" }, { "name" : "Organizational skills" } ], "majorSkills" : "Quality assurance, Study audits, Vendor qualification", "majorSkillsList" : [ "Quality assurance", "Study audits", "Vendor 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reporting of internal process audits, Train Operations staff in quality management", "teamCollaboration" : "Communication point to project teams; 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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PSI divisions; PSI operational offices; Vendors; PSI Operations staff; PSI clients", "domainKnowledge" : "Quality management topics; Contract Research Organization", "domainList" : [ "quality-management-topics", "contract-research-organization" ], "domainSpecificKnowledge" : [ "Quality management topics", "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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Perform quality control audits. 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Boston, Massachusetts, United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "professionalSkills" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement" ], "hardSkillsList" : [ "Batch reviews", "Batch release", "Analytical method validation", "Tech transfers", "Quality agreements", "Supplier qualification", "Auditing", "Monitoring", "CGMP compliance", "Data integrity", "Health authority inspections", "Quality system review", "Product review", "CMC document review", "Drug substance manufacture", "Drug product manufacture", "Solid oral dosage", "Finished goods production", "Finished goods distribution" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Batch reviews", "level" : "intermediate" }, { "name" : "Batch release", "level" : "intermediate" }, { "name" : "Analytical method validation", "level" : "intermediate" }, { "name" : "Tech transfers", "level" : "intermediate" }, { "name" : "Quality agreements", "level" : "intermediate" }, { "name" : "Supplier qualification", "level" : "intermediate" }, { "name" : "Auditing", "level" : "intermediate" }, { "name" : "Monitoring", "level" : "intermediate" }, { "name" : "CGMP compliance", "level" : "intermediate" }, { "name" : "Data integrity", "level" : "intermediate" }, { "name" : "Health authority inspections", "level" : "intermediate" }, { "name" : "Quality system review", "level" : "intermediate" }, { "name" : "Product review", "level" : "intermediate" }, { "name" : "CMC document review", "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" : "Finished goods distribution", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "Quality Assurance, GMP, Clinical programs", "majorSkillsList" : [ "Quality Assurance", "GMP", "Clinical programs" ], "coreResponsibilities" : "Manage quality matters for CMO manufacturing, Manage quality matters for CMO testing, Manage quality matters for CMO release, Lead external quality activities, Support external quality activities, Collaborate with internal CMC functions, Align goals for clinical programs, Align objectives for clinical programs, Ensure cGMP compliance, Realize value-added policies, Realize best practices, Author quality documents, Review quality documents, Approve quality documents, Attend CMO meetings, Attend internal CMC team meetings, Provide quality feedback, Collaborate on complex investigations, Support quality system review meetings, Support product review meetings, Provide data for quality metrics, Provide quality reviews for CMC documents, Provide quality reviews for health authority documents, Review data for compliance, Verify data for compliance, Represent Quality on project teams, Represent Quality at Health Authority Inspections, Represent Quality at supplier meetings, Represent Quality at CMO operational meetings, Represent Quality at QA to QA meetings, Promote quality mindset, Promote quality excellence approach, 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; 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. Manage quality matters for CMO testing", "createdAt" : "2026-06-13T21:38:23.130", "lastUpdated" : "2026-06-15T07:11:51.569", "ingestTimestamp" : "2026-06-13T21:38:23.130", "mongoId" : "6a2c8d9f74d8ee00a097978e", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "150k-200k", "hasSalary" : false, "allSkills" : [ "Batch reviews", "Batch release", "Analytical method validation", "Tech transfers", "Quality agreements", "Supplier qualification", "Auditing", "Monitoring", "CGMP compliance", "Data integrity", "Health authority inspections", "Quality system review", "Product review", "CMC document review", "Drug substance manufacture", "Drug product manufacture", "Solid oral dosage", "Finished goods production", "Finished goods distribution", "Leadership", "Quality Assurance", "GMP", "Clinical programs", "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement", "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" ], "skillCount" : 44, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 838.4529, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2e8e9474d8ee00a0dfb99b", "title" : "Staff Device Quality Engineer", "company" : "Heartflow", "location" : "San Francisco", "locations" : [ "San Francisco" ], "timestamp" : "2026-06-15T11:27:24.678", "fingerprint" : "825c72f62c108d0ef08885919c6eabea73fb3cf6a2b6fbca28e9b3589aba4ee7", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/heartflowinc/jobs/6019212004", "externalId" : "6019212004", "industryFunction" : { }, "structuredLocations" : [ { "city" : "San Francisco", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite" } ], "locationText" : "San Francisco, California, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 6, "experienceMaxYears" : 10, "experienceLevel" : "Lead", "technicalSkills" : "SaMD, AI/ML", "professionalSkills" : [ "Medical technology, coronary artery disease diagnosis and management, AI-driven cardiac test, Software as a Medical Device (SaMD), AI/ML-enabled technologies, global regulatory requirements for medical devices." ], "hardSkillsList" : [ "Software as a Medical Device (SaMD)", "AI/ML-enabled technologies", "QMS architecture", "CAPA program design" ], "softSkillsList" : [ "critical thinking, attention to detail, self-starter, influence without authority" ], "hardSkills" : [ { "name" : "Software as a Medical Device (SaMD)", "level" : "intermediate" }, { "name" : "AI/ML-enabled technologies", "level" : "intermediate" }, { "name" : "QMS architecture", "level" : "intermediate" }, { "name" : "CAPA program design", "level" : "intermediate" } ], "softSkills" : [ { "name" : "critical thinking, attention to detail, self-starter, influence without authority" } ], "majorSkills" : "Software Quality, Design Excellence, Medical Device Regulations, QMS, Risk Management", "majorSkillsList" : [ "Software Quality, Design Excellence, Medical Device Regulations, QMS, Risk Management" ], "coreResponsibilities" : "Serve as the senior technical authority for software quality and design excellence across multiple product lines and platform initiatives. Shape quality engineering practices organization-wide, bridging the gap between rapid Agile development and rigorous medical device regulations. Ensure that software architecture, security, and global regulatory requirements are integrated into every release. Serve as a key decision-maker and escalation point for quality and compliance matters. Strategic oversight and hands-on leadership of the end-to-end design control process within Heartflow’s Software Development Lifecycle (SDLC).", "teamCollaboration" : "Highly cross-functional role requiring collaboration with engineering, regulatory, and product leadership. Mentor and develop Senior and mid-level Quality Engineers.", "projectManagementSkills" : [ "time management" ], "toolProficiency" : [ "FDA, MDSAP" ], "communicationSkills" : "communication; documentation", "documentationSkills" : "documentation", "continuousLearning" : "Actively monitor regulatory landscape changes and proactively update internal practices. Represent Heartflow’s quality and compliance perspective in industry forums, working groups (e.g., IMDRF, FDA Digital Health Center of Excellence engagement), and external partnerships relevant to SaMD and AI/ML regulation.", "problemSolvingSkills" : "system design; risk management; Hazard Analysis; Fault Tree Analysis (FTA)", "specialRequirements" : "Ability to work as a self-starter in a fast-paced, adaptive environment. Serve as the quality sign-off authority for regulatory submissions. Contribute to hiring and capability planning.", "outcomesObjectives" : "Ensure that our digital health solutions—including Software as a Medical Device (SaMD) and AI/ML-enabled technologies—are safe, secure, and compliant. Drive continuous improvement of the QMS, identifying systemic gaps and leading cross-functional initiatives to address them. Ensure DHF completeness and quality across multiple concurrent programs.", "qualificationsBasic" : "Deep expertise in quality systems strategy, including QMS architecture and CAPA program design for SaMD organizations. Demonstrated ability to influence without authority and drive alignment across engineering, regulatory, and product leadership.", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Heartflow is a medical technology company advancing the diagnosis and management of coronary artery disease, the #1 cause of death worldwide, using cutting-edge technology. The flagship product—an AI-driven, non-invasive cardiac test supported by the ACC/AHA Chest Pain Guidelines called the Heartflow FFRCT Analysis—provides a color-coded, 3D model of a patient’s coronary arteries indicating the impact blockages have on blood flow to the heart. Heartflow is the first AI-driven non-invasive integrated heart care solution across the CCTA pathway that helps clinicians identify stenoses in the coronary arteries (RoadMap™Analysis), assess coronary blood flow (FFRCT Analysis), and characterize and quantify coronary atherosclerosis (Plaque Analysis). Our pipeline of products is growing and so is our team; join us in helping to revolutionize precision heartcare. Heartflow is a publicly traded company (HTFL) that has received international recognition for exceptional strides in healthcare innovation, is supported by medical societies around the world, cleared for use in the US, UK, Europe, Japan and Canada, and has been used for more than 500,000 patients worldwide. As a Staff Device Quality Engineer, you will serve as the senior technical authority for software quality and design excellence across multiple product lines and platform initiatives. In this highly cross-functional, strategic role, you will shape quality engineering practices organization-wide, bridging the gap between rapid Agile development and rigorous medical device regulations, ensuring that our digital health solutions—including Software as a Medical Device (SaMD) and AI/ML-enabled technologies—are safe, secure, and compliant. Your core responsibility will be strategic oversight and hands-on leadership of the end-to-end design control process within Heartflow’s Software Development Lifecycle (SDLC). You will ensure that software architecture, security, and global regulatory requirements are integrated into every release, and will serve as a key decision-maker and escalation point for quality and compliance matters. Key Responsibilities Technical Leadership actively monitor regulatory landscape changes and proactively update internal practices. SDLC Architecture define framework strategy and scalability roadmap across the QMS. Agile Integration: Define and champion “Compliance at Speed” frameworks across engineering teams, ensuring Agile sprints meet all regulatory rigor and result in high-quality, predictable releases; develop scalable playbooks and mentor senior engineers on quality-by-design practices. Quality Systems Ownership: Drive continuous improvement of the QMS, identifying systemic gaps and leading cross-functional initiatives to address them. Partner with Quality leadership to influence product strategy, roadmap prioritization, and resource planning. Design Quality establish review criteria and approve outputs. Risk Analysis: Own and govern comprehensive risk management activities, including Hazard Analysis, Fault Tree Analysis (FTA), and Software FMEAs; establish risk management methodology and ensure alignment across all product lines. V develop and govern test strategies, protocols, and reports to ensure product performance, including for novel AI/ML and SaMD modalities. Execution accountable for DHF completeness and quality across multiple concurrent programs. Audit Leadership: Lead and coordinate the organization during internal and external audits (e.g., FDA, Notified Body, MDSAP) as a primary subject matter expert for software processes; develop audit readiness programs and host regulatory agency interactions. Cross-Functional Collaboration serve as the quality sign-off authority for regulatory submissions. Team Development mentor and develop Senior and mid-level Quality Engineers, and contribute to hiring and capability planning. Thought Leadership: Represent Heartflow’s quality and compliance perspective in industry forums, working groups (e.g., IMDRF, FDA Digital Health Center of Excellence engagement), and external partnerships relevant to SaMD and AI/ML regulation. Skills Needed Strong critical thinking skills and great attention to detail. Ability to work as a self-starter in a fast-paced, adaptive environment. Excellent communication, documentation, and time management skills. Demonstrated ability to influence without authority and drive alignment across engineering, regulatory, and product leadership. Deep expertise in quality systems strategy, including QMS architecture and CAPA program design for SaMD organizations. Educational Requirements LI-Hybrid Heartflow is an Equal Opportunity Employer. We are committed to a work environment that supports, inspires, and respects all individuals and do not discriminate against any employee or applicant because of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. This policy applies to every aspect of employment at Heartflow, including recruitment, hiring, training, relocation, promotion, and termination. Positions posted for Heartflow are not intended for or open to third party recruiters / agencies. Submission of any unsolicited resumes for these positions will be considered to be free referrals. Heartflow has become aware of a fraud where unknown entities are posing as Heartflow recruiters in an attempt to obtain personal information from individuals as part of our application or job offer process. Before providing any personal information to outside parties, please verify the following: A) all legitimate Heartflow recruiter email addresses end with “@heartflow.com” and B) the position described is found on our careers site at www.heartflow.com/about/careers/.", "summaryDescription" : "Staff Device Quality Engineer at Heartflow. Skills: Software Quality, Design Excellence, Medical Device Regulations, QMS, Risk Management. Serve as the senior technical authority for software quality and design excellence across multiple product lines and platform initiatives. Shape quality engineering practices organization-wide, bridging the gap between rapid Agile development and rigorous medical device regulations. Ensure that software architecture, security, and global regulatory requiremen", "postedDate" : "2026-06-14T21:41:27.555", "createdAt" : "2026-06-14T21:41:27.555", "lastUpdated" : "2026-06-15T11:27:24.678", "ingestTimestamp" : "2026-06-14T21:41:27.555", "mongoId" : "6a2e8e9474d8ee00a0dfb99b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "hasSalary" : false, "allSkills" : [ "Software as a Medical Device (SaMD)", "AI/ML-enabled technologies", "QMS architecture", "CAPA program design", "critical thinking, attention to detail, self-starter, influence without authority", "Software Quality, Design Excellence, Medical Device Regulations, QMS, Risk Management", "Medical technology, coronary artery disease diagnosis and management, AI-driven cardiac test, Software as a Medical Device (SaMD), AI/ML-enabled technologies, global regulatory requirements for medical devices.", "time management", "FDA, MDSAP" ], "skillCount" : 9, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Executive", "dataQualityScore" : 0.8888889, "_score" : 819.845, "daysOld" : 0, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.97 }, { "id" : "6a2df5aa74d8ee00a0cf6942", "title" : "Quality Auditor", "company" : "Jabil", "location" : "Memphis, TN", "locations" : [ "Memphis, TN", "United States of America" ], "timestamp" : "2026-06-15T10:28:20.568", "fingerprint" : "c2133acba5408cf1cacfaa05cc2d6beeb8d3a446a1843c958259f6588404e1ef", "source" : "workday", "applyUrl" : "https://jabil.wd5.myworkdayjobs.com/Jabil_Careers/job/Memphis-TN/Quality-Auditor_J2453643", "externalId" : "J2453643", "industryFunction" : { }, "locationPoint" : "40.45781,-92.17129", "structuredLocations" : [ { "city" : "Memphis", "state" : "Tennessee", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite" } ], "locationText" : "Memphis, Tennessee, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 0, "experienceMaxYears" : 1, "experienceLevel" : "Entry", "hardSkillsList" : [ "quality control", "audits" ], "softSkillsList" : [ "effective presentation, problem definition, data collection, drawing conclusions" ], "hardSkills" : [ { "name" : "quality control", "level" : "intermediate" }, { "name" : "audits", "level" : "intermediate" } ], "softSkills" : [ { "name" : "effective presentation, problem definition, data collection, drawing conclusions" } ], "majorSkills" : "PC skills", "majorSkillsList" : [ "PC skills" ], "coreResponsibilities" : "The Quality Auditor is responsible for conducting routine quality control audits to ensure conformance with established processes, standards, and procedures. This role involves auditing methods, sequences, and set-ups against manufacturer specifications and requirements, reporting audit results to supervisors and management, and following up on necessary recommendations.", "toolProficiency" : [ "Windows, Jabil software" ], "communicationSkills" : "respond to questions; write correspondence; read visual aid; read instructions; read memos", "problemSolvingSkills" : "define problems; collect data; draw valid conclusions", "specialRequirements" : "Beware of fraud: Jabil will only contact applicants via official job portals with a jabil.com email or direct phone call from a Jabil representative. Jabil does not request payment for interviews or personal identifying information via phone or email. Report any scam listings. Jabil is an equal opportunity employer. Accessibility accommodation is available upon request for individuals with disabilities.", "qualificationsBasic" : "Requires the ability to effectively present information and respond to questions from various groups. Must be able to define problems, collect data, establish facts, and draw valid conclusions. Proficiency in operating a personal computer with a Windows-based operating system and related software is necessary, along with advanced PC skills and knowledge of Jabil's software packages. The role also requires the ability to write simple correspondence, read and understand visual aids, and apply common sense understanding to carry out simple instructions in standardized situations. Basic arithmetic skills including addition, subtraction, multiplication, division, and the ability to compute rate, ratio, and percent, along with interpreting graphs, are essential.", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "At Jabil (NYSE: JBL), we are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, supply chain, and manufacturing solutions. With 60 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe. **JOB SUMMARY** Has responsibility for quality control audits that are in conformance with quality processes, standards and procedures **ESSENTIAL DUTIES AND RESPONSIBILITIES** · Performs routine audits and reports · Audits methods, sequences, set-ups to ensure the conformance and specifications to the manufacturer's required processes. · Conducts routine manufacturer's audits; audits the quality of the product to ensure the conformance specifications and the requirements of the process; · Conducts audits in all manufacturer's processes and maintenance; · Provides to supervisor and management results from the audits · Follows up with the required recommendations. · May perform other duties and responsibilities as assigned. **JOB QUALIFICATIONS** **KNOWLEDGE REQUIREMENTS** · Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public. · Ability to define problems, collect data, establish facts, and draw valid conclusions. · Ability to operate a personal computer including using a Windows based operating system and related software. · Advanced PC skills, including training and knowledge of Jabil’s software packages. · Ability to write simple correspondence. Read and understand visual aid. · Ability to apply common sense understanding to carry out simple one- or two-step instructions. · Ability to deal with standardized situations with only occasional or no variables. · Ability to read and comprehend simple instructions, short correspondence, and memos. · Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. · Ability to compute rate, ratio, and percent and to draw and interpret graphs. BE AWARE OF FRAUD: When applying for a job at Jabil you will be contacted via correspondence through our official job portal with a jabil.com e-mail address; direct phone call from a member of the Jabil team; or direct e-mail with a jabil.com e-mail address. Jabil does not request payments for interviews or at any other point during the hiring process. Jabil will not ask for your personal identifying information such as a social security number, birth certificate, financial institution, driver’s license number or passport information over the phone or via e-mail. If you believe you are a victim of identity theft, contact the Federal Bureau of Investigations internet crime hotline (www.ic3.gov), the Federal Trade Commission identity theft hotline (www.identitytheft.gov) and/or your local police department. Any scam job listings should be reported to whatever website it was posted in. **Jabil, including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, age, disability, genetic information, veteran status, or any other characteristic protected by law.** # **Accessibility Accommodation** If you are a qualified individual with a disability, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access Jabil.com/Careers site as a result of your disability. You can request a reasonable accommodation by sending an e-mail to Always_Accessible@Jabil.com or calling 727-803-7988 with the nature of your request and contact information. Please do not direct any other general employment related questions to this e-mail or phone number. Please note that only those inquiries concerning a request for reasonable accommodation will be responded to. #whereyoubelong #AWorldofPossibilities #EarlyCareer", "summaryDescription" : "Quality Auditor at Jabil. Skills: PC skills. The Quality Auditor is responsible for conducting routine quality control audits to ensure conformance with established processes, standards, and procedures. This role involves auditing methods, sequences, and set-ups against manufacturer specifications and requirements, reporting audit results to supervisors and management, and following up on necessary recommendations.", "postedDate" : "2026-06-13T19:18:34.006", "createdAt" : "2026-06-14T19:18:33.988", "lastUpdated" : "2026-06-15T10:28:20.568", "ingestTimestamp" : "2026-06-14T19:18:33.988", "mongoId" : "6a2df5aa74d8ee00a0cf6942", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://jabil.wd5.myworkdayjobs.com/Jabil_Careers/job/Memphis-TN/Quality-Auditor_J2453643", "hasSalary" : false, "allSkills" : [ "quality control", "audits", "effective presentation, problem definition, data collection, drawing conclusions", "PC skills", "Windows, Jabil software" ], "skillCount" : 5, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 794.1452, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Manufacturing", "llmIndustryConfidence" : 0.95 }, { "id" : "69cf3f072beec4dd3d93425c", "title" : "Quality Auditor", "company" : "Amazon Japan G. K.", "industry" : "Administrative Support, Machine Learning Data Operatio, Artificial Intelligence", "salary" : { "min" : 5500000.0, "max" : 8000000.0, "currency" : "JPY", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Quality Auditor in Osaka, Japan, adjusted for the technology industry and a large company size." }, "location" : "Osaka, JPN", "locations" : [ "Osaka, JPN" ], "timestamp" : "2026-06-15T05:38:57.904", "fingerprint" : "942cdcfadf30b7eddc0e4391eac24bcfb57a4bd767d879d4554a572922943b7c", "source" : "amazon", "language" : "ko", "applyUrl" : "https://account.amazon.com/jobs/10381696/apply", "externalId" : "fe9301dd-c57c-4e21-8be8-e1078cf37b3a", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Osaka", "country" : "Japan", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "34.6937569,135.5014539" } ], "locationText" : "Osaka, Japan", "employmentType" : "FULL_TIME", "professionalSkills" : [ "Data annotation", "Quality evaluation", "Quality measurement" ], "hardSkillsList" : [ "Quality auditing", "Root cause analysis", "Manual review" ], "hardSkills" : [ { "name" : "Quality auditing", "level" : "intermediate" }, { "name" : "Root cause analysis", "level" : "intermediate" }, { "name" : "Manual review", "level" : "intermediate" } ], "majorSkills" : "Korean language, Quality assurance, Data quality", "majorSkillsList" : [ "Korean language", "Quality assurance", "Data quality" ], "coreResponsibilities" : "Perform quality audits, Conduct manual reviews, Support performance improvement, Conduct detailed analysis, Identify root causes of issues, Ensure accurate documentation, Ensure efficient reporting, Conduct audits for deep-dive investigations, Conduct audits for escalation handling, Maintain strict adherence to quality standards, Maintain strict adherence to procedures, Collaborate with Quality Audit Specialists, Implement process improvements, Implement best practices, Contribute to continuous improvement initiatives", "teamCollaboration" : "Quality Audit Specialists; Quality Assurance team", "domainKnowledge" : "AI development; AI training; Data quality standards", "domainList" : [ "ai-development", "ai-training", "data-quality-standards" ], "domainSpecificKnowledge" : [ "AI development", "AI training", "Data quality standards" ], "documentationSkills" : "Documentation of quality findings; Reporting of quality findings", "continuousLearning" : "Continuous improvement initiatives", "problemSolvingSkills" : "Root cause analysis", "qualificationsBasic" : "Native-level Korean proficiency, Business-level Japanese or English, Experience in data annotation, Experience in operations, Experience in production-driven work, Experience working collaboratively in a team", "qualificationsPreferred" : "Experience following guidelines, Experience adhering to defined processes, Adaptability to changing priorities, Adaptability to changing workload, High attention to detail, High accuracy, Tech-sector QA background, Familiarity with AI/ML fundamentals, Prior experience with speech data, Prior experience with language data", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "AGI-DS 팀에서는 세부 사항까지 꼼꼼하게 확인할 수 있는 한국어 품질 감사 담당자(Quality Auditor, 계약직)를 모집하고 있습니다. 본 역할에서는 글로벌 Data Associate 네트워크 내에서 체계적인 품질 평가를 수행하며, 자동화된 품질 측정 시스템의 정확성을 검증하기 위한 수동 리뷰를 진행하게 됩니다. 이 포지션은 AI 개발 및 학습을 위한 데이터 품질의 높은 기준을 유지하는 데 핵심적인 역할을 담당합니다. The AGI-DS team is seeking a Korean Quality Auditor (Contact employee)with a strong attention to detail. In this role, you will perform systematic quality evaluations within our global Data Associate network and conduct manual reviews to validate our automated quality measurement systems. This position is essential to maintaining high standards of data quality for AI development and training. Key job responsibilities *Data Associate가 제출한 개별 워크플로우 및 산출물에 대해 품질 감사를 수행합니다. *온사이트 Data Associate의 성과 향상을 위해 코칭 및 캘리브레이션을 지원합니다. *Data Associate 레벨에서의 품질을 상세히 검수하고, 문제의 근본 원인을 식별합니다. *자동화된 품질 측정 시스템의 정확성을 검증하기 위해 수동 리뷰를 수행합니다. *품질 분석 결과에 대한 정확하고 효율적인 문서화 및 보고를 수행합니다. *심층 조사(Deep-dive) 및 에스컬레이션 대응을 위한 감사를 수행합니다. *품질 기준 및 절차를 철저히 준수합니다. *프로세스 개선 및 베스트 프랙티스 도입을 위해 Quality Audit Specialist와 긴밀히 협업합니다. *Quality Assurance 팀 내 지속적인 개선 활동에 기여합니다. *Perform quality audits on individual workflows and deliverables submitted by Data Associates. *Support performance improvement for on-site Data Associates through coaching and calibration. *Conduct detailed analysis of quality at the Data Associate level and identify root causes of issues. *Perform manual reviews to validate automated quality measurement systems. *Ensure accurate and efficient documentation and reporting of quality findings. *Conduct audits for deep-dive investigations and escalation handling. *Maintain strict adherence to quality standards and procedures. *Collaborate closely with Quality Audit Specialists to implement process improvements and best practices. *Contribute to continuous improvement initiatives within the Quality Assurance team. Basic Qualifications: - 한국어가 모국어 수준이며, 일본어 또는 영어로 비즈니스 레벨 수준이신 분 (읽기, 쓰기, 말하기, 듣기) - 데이터 어노테이션, 운영(Operations) 또는 이와 유사한 생산 중심 업무 경험 우대 - 팀 환경에서 협업하여 근무한 경험 - Native-level proficiency in Korean, with business-level proficiency in Japanese or English (reading, writing, speaking, and listening). - Experience in data annotation, operations, or similar production-driven work preferred - Experience working collaboratively in a team environment Preferred Qualifications: - 가이드라인을 준수하고 정해진 프로세스에 따라 업무를 수행한 경험 - 변화하는 우선순위와 업무량에 유연하게 대응할 수 있는 분 - 높은 수준의 정확성과 세밀함을 갖추신 분 - 테크 산업 내 QA(품질 보증) 관련 경험 보유자 - AI/ML 기초에 대한 이해 보유자 - 음성 또는 언어 데이터 관련 경험 보유자 - Experience following guidelines and adhering to defined processes - Adaptability to changing priorities and workload - High attention to detail and accuracy - Tech-sector QA background. - Familiarity with AI/ML fundamentals. - Prior experience with speech or language data. 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 Auditor at Amazon Japan G. K.. Skills: Korean language, Quality assurance, Data quality. Perform quality audits. Conduct manual reviews", "postedDate" : "2026-06-13T17:12:44.171", "createdAt" : "2026-06-13T17:12:44.171", "lastUpdated" : "2026-06-15T05:38:57.904", "ingestTimestamp" : "2026-06-13T17:12:44.171", "mongoId" : "69cf3f072beec4dd3d93425c", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.com/jobs/10381696/apply", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Quality auditing", "Root cause analysis", "Manual review", "Korean language", "Quality assurance", "Data quality", "Data annotation", "Quality evaluation", "Quality measurement", "AI development", "AI training", "Data quality standards" ], "skillCount" : 12, "jobCategory" : "operations", "dataQualityScore" : 0.8888889, "_score" : 792.026, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a30895df292fd229c0937e0", "title" : "Quality Auditor - 2nd Shift", "company" : "Bosch-HomeComfort", "industry" : "Mechanical Or Industrial Engineering", "salary" : { "min" : 65000.0, "max" : 85000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Quality Auditor in Wichita, United States, adjusted for the manufacturing industry and full-time onsite work mode." }, "location" : "Wichita, KS, United States", "locations" : [ "Wichita", "KS", "United States" ], "timestamp" : "2026-06-16T08:46:16.459", "fingerprint" : "e55241d155336b959c4621d2134e17f7a32c03bc9f99dc8494680be9358ec9de", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/Bosch-HomeComfort/744000132075549-quality-auditor-2nd-shift", "externalId" : "744000132075549", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Wichita", "state" : "Kansas", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "37.6922361,-97.3375448" } ], "locationText" : "Wichita, Kansas, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "High School", "experienceMinYears" : 2, "experienceMaxYears" : 5, "experienceLevel" : "mid", "professionalSkills" : [ "Quality control", "Process improvement", "Data analysis" ], "hardSkillsList" : [ "Quality inspection", "Measurement techniques", "Documentation" ], "softSkillsList" : [ "Problem solving" ], "hardSkills" : [ { "name" : "Quality inspection", "level" : "intermediate" }, { "name" : "Measurement techniques", "level" : "intermediate" }, { "name" : "Documentation", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Problem solving" } ], "majorSkills" : "Quality assurance, Process monitoring", "majorSkillsList" : [ "Quality assurance", "Process monitoring" ], "coreResponsibilities" : "Perform quality inspections on incoming materials, Monitor production processes for quality compliance, Conduct in-process and final product inspections, Document inspection results and non-conformance issues, Identify and report quality deviations, Assist in root cause analysis of quality problems, Participate in continuous improvement initiatives, Maintain quality records and documentation", "teamCollaboration" : "Production team; Quality department", "domainKnowledge" : "Quality control procedures; Manufacturing processes", "domainList" : [ "quality-control-procedures", "manufacturing-processes" ], "domainSpecificKnowledge" : [ "Quality control procedures", "Manufacturing processes" ], "toolProficiency" : [ "Microsoft Office Suite" ], "communicationSkills" : "Reporting; Documentation", "documentationSkills" : "Quality records; Inspection reports", "problemSolvingSkills" : "Root cause analysis", "specialRequirements" : "Second shift availability", "outcomesObjectives" : "Ensure product quality standards; Minimize quality defects; Support production efficiency", "qualificationsBasic" : "High School diploma or GED, 2+ years of experience in a quality role, Experience with quality control procedures, Ability to read and interpret technical documents, Basic computer skills", "qualificationsPreferred" : "Experience with statistical process control (SPC), Knowledge of ISO 9001 standards, Experience with calibration procedures, Familiarity with lean manufacturing principles", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "We Are Bosch. At Bosch, we shape the future by inventing high-quality technologies and services that spark enthusiasm and enrich people’s lives. Our areas of activity are every bit as diverse as our outstanding Bosch teams around the world. Their creativity is the key to innovation through connected living, mobility, or industry. Let’s grow together, enjoy more, and inspire each other. Work #LikeABosch • Reinvent yourself: At Bosch, you will evolve. • Discover new directions: At Bosch, you will find your place. • Balance your life: At Bosch, your job matches your lifestyle. • Celebrate success: At Bosch, we celebrate you. • Be yourself: At Bosch, we value values. • Shape tomorrow: At Bosch, you change lives. Bosch Home Solutions is seeking a Quality Auditor. This position performs quality audits on finished goods, purchased parts, in-process parts, and subassemblies. Assists in troubleshooting equipment and performs testing and calibration activities to ensure compliance with quality standards. Key Responsibilities * Read, communicate, and understand Operational Method Sheets (OMS) and job instructions * Perform partial disassembly of finished goods using hand tools for inspection purposes * Conduct assembly/disassembly operations such as drilling, screwing, and bolting * Use precision tools including gauges, indicators, micrometers, measuring tapes, scales, and testing equipment * Utilize systems such as computers and AS400 for documentation and tracking * Perform audits on manufacturing processes, procedures, work instructions, and specifications * Inspect purchased parts and materials as required * Identify and report abnormal quality conditions * Complete inspection reports and tagging requirements * Follow all safety protocols and company procedures. * Other duties as assigned. ## Qualifications * High school diploma or equivalent required * Previous experience in Quality, Inspection, testing preferred * Ability to read OMS and quality specifications * Excellent attention to detail * Commitment to workplace safety and continuous improvement support ## Additional Information Equal Opportunity Employer, including disability / veterans *Bosch adheres to Federal, State, and Local laws regarding drug-testing. Employment is contingent upon the successful completion of a drug screen and background check. Candidates who have been offered the position must pass both screenings before their start date. Note: While performing the duties of this position, associates are regularly exposed to vibration and frequent exposure to moving mechanical parts. Occasional exposure to fumes or airborne particles. Noise levels are typically loud. *The above profile and description are not intended to include all details of the position. Your well-being matters at Bosch! We offer a competitive compensation and a benefits package designed to empower you in every area of your life. This includes premium health coverage, a 401(k) with generous matching, resources for financial planning and goal setting, ample paid time off, parental leave, and comprehensive life and disability protection. We're investing in your success!", "summaryDescription" : "Quality Auditor - 2nd Shift at Bosch-HomeComfort. Skills: Quality assurance, Process monitoring. Perform quality inspections on incoming materials. Monitor production processes for quality compliance", "postedDate" : "2026-06-14T18:49:49.000", "createdAt" : "2026-06-16T01:42:34.739", "lastUpdated" : "2026-06-16T08:46:16.459", "ingestTimestamp" : "2026-06-16T01:42:34.739", "mongoId" : "6a30895df292fd229c0937e0", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 65000, "salaryAnnualMax" : 85000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Quality inspection", "Measurement techniques", "Documentation", "Problem solving", "Quality assurance", "Process monitoring", "Quality control", "Process improvement", "Data analysis", "Quality control procedures", "Manufacturing processes", "Microsoft Office Suite" ], "skillCount" : 12, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 1.0, "_score" : 755.3935, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Manufacturing", "llmIndustryConfidence" : 0.95 }, { "id" : "6a30714cf292fd229cff899a", "title" : "Quality Auditor - 2nd Shift", "company" : "Bosch-HomeComfort", "industry" : "Mechanical Or Industrial Engineering", "salary" : { "min" : 57000.0, "max" : 78000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Quality Auditor in Wichita, United States, adjusted for the manufacturing industry and full-time onsite work mode." }, "location" : "Wichita, KS, United States", "locations" : [ "Wichita", "KS", "United States" ], "timestamp" : "2026-06-16T13:11:14.963", "fingerprint" : "f499917f25058089d54bc2e11a77fa3b7d49859d375a319da72ab5cc3ddd53cb", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/Bosch-HomeComfort/744000132075549-quality-auditor-2nd-shift", "externalId" : "744000132075549", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Wichita", "state" : "Kansas", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "37.6922361,-97.3375448" } ], "locationText" : "Wichita, Kansas, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "High school diploma or equivalent", "experienceMinYears" : 2, "experienceMaxYears" : 5, "experienceLevel" : "mid", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "We Are Bosch. At Bosch, we shape the future by inventing high-quality technologies and services that spark enthusiasm and enrich people’s lives. Our areas of activity are every bit as diverse as our outstanding Bosch teams around the world. Their creativity is the key to innovation through connected living, mobility, or industry. Let’s grow together, enjoy more, and inspire each other. Work #LikeABosch • Reinvent yourself: At Bosch, you will evolve. • Discover new directions: At Bosch, you will find your place. • Balance your life: At Bosch, your job matches your lifestyle. • Celebrate success: At Bosch, we celebrate you. • Be yourself: At Bosch, we value values. • Shape tomorrow: At Bosch, you change lives. Bosch Home Solutions is seeking a Quality Auditor. This position performs quality audits on finished goods, purchased parts, in-process parts, and subassemblies. Assists in troubleshooting equipment and performs testing and calibration activities to ensure compliance with quality standards. Key Responsibilities * Read, communicate, and understand Operational Method Sheets (OMS) and job instructions * Perform partial disassembly of finished goods using hand tools for inspection purposes * Conduct assembly/disassembly operations such as drilling, screwing, and bolting * Use precision tools including gauges, indicators, micrometers, measuring tapes, scales, and testing equipment * Utilize systems such as computers and AS400 for documentation and tracking * Perform audits on manufacturing processes, procedures, work instructions, and specifications * Inspect purchased parts and materials as required * Identify and report abnormal quality conditions * Complete inspection reports and tagging requirements * Follow all safety protocols and company procedures. * Other duties as assigned. ## Qualifications * High school diploma or equivalent required * Previous experience in Quality, Inspection, testing preferred * Ability to read OMS and quality specifications * Excellent attention to detail * Commitment to workplace safety and continuous improvement support ## Additional Information Equal Opportunity Employer, including disability / veterans *Bosch adheres to Federal, State, and Local laws regarding drug-testing. Employment is contingent upon the successful completion of a drug screen and background check. Candidates who have been offered the position must pass both screenings before their start date. Note: While performing the duties of this position, associates are regularly exposed to vibration and frequent exposure to moving mechanical parts. Occasional exposure to fumes or airborne particles. Noise levels are typically loud. *The above profile and description are not intended to include all details of the position. Your well-being matters at Bosch! We offer a competitive compensation and a benefits package designed to empower you in every area of your life. This includes premium health coverage, a 401(k) with generous matching, resources for financial planning and goal setting, ample paid time off, parental leave, and comprehensive life and disability protection. We're investing in your success!", "summaryDescription" : "Quality Auditor - 2nd Shift at Bosch-HomeComfort", "postedDate" : "2026-06-14T18:49:49.000", "createdAt" : "2026-06-16T01:31:28.493", "lastUpdated" : "2026-06-16T13:11:14.963", "ingestTimestamp" : "2026-06-16T01:31:28.493", "mongoId" : "6a30714cf292fd229cff899a", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 57000, "salaryAnnualMax" : 78000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.8888889, "_score" : 750.39124, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Manufacturing", "llmIndustryConfidence" : 0.95 }, { "id" : "68ed10aa70f0b99d58e7b9cd", "title" : "Device Associate, Quality Services, Device Tech Support", "company" : "Amazon Development Centre (India) Private Limited", "industry" : "Operations, IT, Support Engineering, Device Associates, alexa and amazon devices", "salary" : { "min" : 450000.0, "max" : 750000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on the market baseline for an entry-level Device Associate, Quality Services, Device Tech Support role in Chennai, India, with adjustments for the technology industry and company size." }, "location" : "Chennai, Tamil Nadu, IND", "locations" : [ "Chennai, Tamil Nadu, IND" ], "timestamp" : "2026-06-16T02:21:26.475", "fingerprint" : "eb47b7319eabf844f4e944767d1bfdabc851e0d483daaf0825e0b50f6810af9f", "source" : "amazon", "language" : "en", "applyUrl" : "https://account.amazon.com/jobs/3105294/apply", "externalId" : "e72b767d-d712-462d-bbc1-ef7aac77d379", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Chennai", "state" : "Tamil Nadu", "country" : "India", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "13.0836939,80.2701860" } ], "locationText" : "Chennai, Tamil Nadu, India", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "coreResponsibilities" : "Execute test plans, Execute test cases, Create test data, Report results, Understand product functionality, Stay connected with changing requirements, Stay connected with documentation, Actively look for gaps, Look beyond test cases for issues, Execute processes to test product changes, Backtrack bugs, Backtrack issues, Do root cause analysis of bugs, Do root cause analysis of issues, Execute regression cases, Raise bugs, Support ad-hoc requests, Interact with QA for new features, Support first pass, Support bug repro, Contribute ideas, Take part in implementing ideas", "teamCollaboration" : "Interacting with QA", "domainKnowledge" : "E-reader devices", "domainList" : [ "e-reader-devices" ], "domainSpecificKnowledge" : [ "E-reader devices" ], "problemSolvingSkills" : "Root cause analysis", "qualificationsBasic" : "Bachelor's degree, Knowledge of QA methodology, Knowledge of QA tools", "qualificationsPreferred" : "Good Communication, Testing Knowledge, Good Analytical Skill", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "At this role the associate gets a chance to work on multiple generations of E-reader devices and will directly contribute to the high quality of the devices. Key job responsibilities - Execute test plans & test cases, creating test data, and reporting results in a timely, clear, and concise manner. - Should have understanding of the functionality of the project/product. Should have the ability to stay connected with changing requirements and documentation. - Should be able to actively look for gaps in test cases and look beyond test cases for issues/bugs. - Should execute processes to thoroughly test product changes. - Should have the ability to backtrack and do a root cause analysis of bugs/issues. A day in the life A typical day involves executing regression cases , raising bugs, supporting ad-hoc requests etc. Also involves interacting with QA for new features, supporting first pass and bug repro. Contributing ideas and take part in implementing them About the team Highly energetic and fun loving team with great flexibility. Team contributes to multiple aspect of the quality of E-reader devices. Handles multiple parallel releases successfully. Basic Qualifications: - Bachelor's degree - Knowledge of QA methodology and tools Preferred Qualifications: - Good Communication - Testing Knowledge - Good Analytical Skill 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" : "Device Associate, Quality Services, Device Tech Support at Amazon Development Centre (India) Private Limited. Execute test plans. Execute test cases", "postedDate" : "2026-06-14T20:31:14.524", "createdAt" : "2026-06-14T20:31:14.524", "lastUpdated" : "2026-06-16T02:21:26.475", "ingestTimestamp" : "2026-06-14T20:31:14.524", "mongoId" : "68ed10aa70f0b99d58e7b9cd", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.com/jobs/3105294/apply", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "E-reader devices" ], "skillCount" : 1, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Entry", "dataQualityScore" : 0.8888889, "_score" : 725.6593, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.95 }, { "id" : "68ed10aa70f0b99d58e7b9ef", "title" : "Device Associate, Quality Services, Device Tech Support", "company" : "Amazon Development Centre (India) Private Limited", "industry" : "Operations, IT, Support Engineering, Device Associates, alexa and amazon devices", "salary" : { "min" : 450000.0, "max" : 750000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on the market baseline for an entry-level Device Associate, Quality Services, Device Tech Support role in Chennai, India, with adjustments for the technology industry and company size." }, "location" : "Chennai, Tamil Nadu, IND", "locations" : [ "Chennai, Tamil Nadu, IND" ], "timestamp" : "2026-06-16T05:47:42.478", "fingerprint" : "9b990b562052a47b0d6ce9c4fdd6b00cfb29c1d780d676b8f1618e70495e8fb8", "source" : "amazon", "language" : "en", "applyUrl" : "https://account.amazon.com/jobs/3105254/apply", "externalId" : "e1f35ec7-0ba1-41b8-b924-a9a56904cd2a", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Chennai", "state" : "Tamil Nadu", "country" : "India", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "13.0836939,80.2701860" } ], "locationText" : "Chennai, Tamil Nadu, India", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "coreResponsibilities" : "Execute test plans, Execute test cases, Create test data, Report results, Understand project functionality, Understand product functionality, Stay connected with changing requirements, Stay connected with documentation, Actively look for gaps, Look beyond test cases for issues, Execute processes to test product changes, Backtrack bugs, Backtrack issues, Perform root cause analysis of bugs, Perform root cause analysis of issues, Execute regression cases, Raise bugs, Support ad-hoc requests, Interact with QA for new features, Support first pass, Support bug repro, Contribute ideas, Implement ideas", "teamCollaboration" : "Interacting with QA", "domainKnowledge" : "E-reader devices", "domainList" : [ "e-reader-devices" ], "domainSpecificKnowledge" : [ "E-reader devices" ], "problemSolvingSkills" : "Root cause analysis", "qualificationsBasic" : "Bachelor's degree, Knowledge of QA methodology, Knowledge of QA tools", "qualificationsPreferred" : "Bachelor's degree in business economics, Bachelor's degree in engineering, Bachelor's degree in analytics, Bachelor's degree in mathematics, Bachelor's degree in statistics, Bachelor's degree in information technology, CMA, Good Communication, Testing Knowledge, Good Analytical Skill", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "At this role the associate gets a chance to work on multiple generations of E-reader devices and will directly contribute to the high quality of the devices. Key job responsibilities - Execute test plans & test cases, creating test data, and reporting results in a timely, clear, and concise manner. - Should have understanding of the functionality of the project/product. Should have the ability to stay connected with changing requirements and documentation. - Should be able to actively look for gaps in test cases and look beyond test cases for issues/bugs. - Should execute processes to thoroughly test product changes. - Should have the ability to backtrack and do a root cause analysis of bugs/issues. A day in the life A typical day involves executing regression cases , raising bugs, supporting ad-hoc requests etc. Also involves interacting with QA for new features, supporting first pass and bug repro. Contributing ideas and take part in implementing them About the team Highly energetic and fun loving team with great flexibility. Team contributes to multiple aspect of the quality of E-reader devices. Handles multiple parallel releases successfully. Basic Qualifications: - Bachelor's degree - Knowledge of QA methodology and tools Preferred Qualifications: - Bachelor's degree in business economics, engineering, analytics, mathematics, statistics, information technology or equivalent, or CMA - Good Communication - Testing Knowledge - Good Analytical Skill 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" : "Device Associate, Quality Services, Device Tech Support at Amazon Development Centre (India) Private Limited. Execute test plans. Execute test cases", "postedDate" : "2026-06-14T19:59:28.514", "createdAt" : "2026-06-14T19:59:28.514", "lastUpdated" : "2026-06-16T05:47:42.478", "ingestTimestamp" : "2026-06-14T19:59:28.514", "mongoId" : "68ed10aa70f0b99d58e7b9ef", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.com/jobs/3105254/apply", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "E-reader devices" ], "skillCount" : 1, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Entry", "dataQualityScore" : 0.8888889, "_score" : 723.7459, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.95 }, { "id" : "6a15e46d58b93c861e7c6f0e", "title" : "Contract Quality Records Auditor", "company" : "Embraer", "industry" : "Manufacturing", "salary" : { "min" : 75000.0, "max" : 105000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Mid-seniority Contract Quality Records Auditor in Macon, United States, within the Manufacturing industry." }, "location" : "Macon, GA", "locations" : [ "Macon", "GA" ], "timestamp" : "2026-06-16T04:55:33.341", "fingerprint" : "8b5a3413eb6c16801dd6827f3846b1615789a6d68e28217a61026067496ef039", "source" : "breezyhr", "language" : "en", "applyUrl" : "https://embraer.breezy.hr/p/cec4547b5ade-contract-quality-records-auditor", "externalId" : "cec4547b5ade", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Macon", "state" : "Georgia", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "32.8406946,-83.6324022" } ], "locationText" : "Macon, Georgia, United States", "employmentType" : "FULL_TIME", "coreResponsibilities" : "Audit and review documentation prior to aircraft delivery, Verify completeness of maintenance records", "domainKnowledge" : "Aircraft delivery", "domainList" : [ "aircraft-delivery" ], "domainSpecificKnowledge" : [ "Aircraft delivery" ], "qualificationsBasic" : "Completeness of maintenance record verification", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "POSITION SUMMARY The Quality Records Auditor is responsible to the Chief Inspector for auditing and review of all applicable documentation prior to aircraft delivery as detailed in the audit flow process. JOB RESPONSIBILITIES Verifies the completeness of the maintenance record package; ensures that", "summaryDescription" : "Contract Quality Records Auditor at Embraer. Audit and review documentation prior to aircraft delivery. 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Skills: Field service, Medical device repair. Perform installations. Perform repairs", "createdAt" : "2026-06-15T22:26:03.445", "lastUpdated" : "2026-06-16T06:55:14.724", "ingestTimestamp" : "2026-06-15T22:26:03.445", "mongoId" : "6a305c4ff292fd229cf6158b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 75000, "salaryAnnualMax" : 105000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Mechanical repair", "Electrical repair", "Electronic repair", "Field service", "Medical device repair", "Customer service", "Technical support", "Medical device regulations", "Valid driver's license", "Diagnostic tools", "Hand tools" ], "skillCount" : 11, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 0.44444445, "_score" : 710.45465, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a305c4ff292fd229cf61588", "title" : "Field Service Technician / Engineer (Medical Device) - 61", "industry" : "Healthcare", "salary" : { "min" : 75000.0, "max" : 105000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Mid-level Field Service Technician/Engineer in the Healthcare industry in Houston, United States, adjusted for seniority and industry." }, "location" : "Houston, TX", "locations" : [ "Houston, TX" ], "certifications" : [ "Valid driver's license" ], "timestamp" : "2026-06-16T08:30:41.047", "fingerprint" : "acc841e7df91fffa2c0bee4437b2010bb85a4da39c894a81d3b5465825672d0c", "source" : "jazzhr", "language" : "en", "externalId" : "iYhlLj1IXy", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Houston", "state" : "Texas", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "29.7589382,-95.3676974" } ], "locationText" : "Houston, Texas, United States", "technicalSkills" : "Medical device troubleshooting, Electrical troubleshooting, Mechanical troubleshooting, Pneumatic troubleshooting, Hydraulic troubleshooting, Computer hardware, Networking", "professionalSkills" : [ "Field service", "Technical support", "Customer service" ], "hardSkillsList" : [ "Repair", "Maintenance", "Calibration", "Installation", "Troubleshooting" ], "hardSkills" : [ { "name" : "Repair", "level" : "intermediate" }, { "name" : "Maintenance", "level" : "intermediate" }, { "name" : "Calibration", "level" : "intermediate" }, { "name" : "Installation", "level" : "intermediate" }, { "name" : "Troubleshooting", "level" : "intermediate" } ], "majorSkills" : "Medical device repair, Field service engineering", "majorSkillsList" : [ "Medical device repair", "Field service engineering" ], "coreResponsibilities" : "Perform scheduled maintenance, Perform unscheduled repairs, Install new equipment, Calibrate equipment, Troubleshoot equipment failures, Document all service activities, Provide customer training, Manage spare parts inventory", "teamCollaboration" : "Field service team; Customers", "domainKnowledge" : "Medical device regulations; Medical device operation", "domainList" : [ "medical-device-regulations", "medical-device-operation" ], "domainSpecificKnowledge" : [ "Medical device regulations", "Medical device operation" ], "toolProficiency" : [ "Hand tools", "Power tools", "Diagnostic equipment" ], "communicationSkills" : "Customer communication", "documentationSkills" : "Service reports", "continuousLearning" : "Manufacturer training", "problemSolvingSkills" : "Troubleshooting", "specialRequirements" : "25% travel, On-call rotation", "outcomesObjectives" : "Ensure equipment uptime; Maintain customer satisfaction", "qualificationsBasic" : "5+ years experience, Associate's degree, Valid driver's license, Ability to lift 50 lbs", "qualificationsPreferred" : "Bachelor's degree", "workSiteFlexibility" : "Onsite", "summaryDescription" : "Field Service Technician / Engineer (Medical Device) - 61. 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Marketing teams alignment; Product Management alignment", "projectManagementSkills" : [ "Sales plan creation" ], "domainKnowledge" : "EU research landscape; Clinical landscape; EEG technology; Non-invasive brain stimulation; Epilepsy; Stroke; Depression; Alzheimer's; Neuroscience; Neurology; Psychiatry; Rehabilitation; Academic research", "domainList" : [ "eu-research-landscape", "clinical-landscape", "eeg-technology", "non-invasive-brain-stimulation", "epilepsy", "stroke", "depression", "alzheimer-s", "neuroscience", "neurology", "psychiatry", "rehabilitation", "academic-research" ], "domainSpecificKnowledge" : [ "EU research landscape", "Clinical landscape", "EEG technology", "Non-invasive brain stimulation", "Epilepsy", "Stroke", "Depression", "Alzheimer's", "Neuroscience", "Neurology", "Psychiatry", "Rehabilitation", "Academic research" ], "toolProficiency" : [ "CRM" ], "communicationSkills" : "Presentation skills; English communication", "continuousLearning" : "Professional development", "specialRequirements" : "Travel up to 50-60%, Client site visits, Clinical trials", "outcomesObjectives" : "Hit sales targets; Exceed sales targets", "qualificationsBasic" : "3 years of experience, Hunter mentality, Proven track record sales targets EU, Bachelor's degree business, Technical or scientific background, Clinical understanding EEG technology, Routine EEG knowledge, Ambulatory EEG knowledge, LTM knowledge, CEEG in ICU knowledge, Creating and executing sales plan, Analysing data, Reporting on progress, Excellent English communication, Excellent English presentation skills, Willingness to travel 50-60%", "qualificationsPreferred" : "Experience selling medical devices, Experience selling scientific instruments, Experience selling research equipment, Direct experience EEG, Direct experience neurostimulation, Direct experience neuroimaging, Direct experience neuroscience technology, Established network neuroscience, Established network neurology, Established network psychiatry, Established network rehabilitation, Established network academic research, Clinical background, Scientific background neuroscience, Scientific background biomedical engineering, Scientific background psychology", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Who we are At Neuroelectrics® we are on a mission to change brain health forever. We design and manufacture wearable medical devices that monitor and modulate brain activity — combining high-density EEG with non-invasive neurostimulation to help researchers and clinicians tackle some of the most challenging neurological and psychiatric conditions, from epilepsy and stroke to depression and Alzheimer's. Our technology is used in leading universities, hospitals and research centres in more than 30 countries, and we are now expanding our commercial footprint in the United Kingdom. Position Summary We are looking for a Sales Manager to lead our commercial activity. This is a strategic, hands-on role for an experienced sales professional who knows the EU research and clinical landscape, enjoys representing breakthrough technology, and wants the autonomy of a self-employed contract. You will own the Spanish market end-to-end — building the pipeline, closing deals and acting as the local face of Neuroelectrics for universities, hospitals, research institutes and key opinion leaders. What will you do Develop and execute the Spanish sales plan for our EEG and non-invasive brain stimulation portfolio. Build and nurture a strong pipeline across academic, clinical and research institutions. Lead the full sales cycle: prospecting, qualification, technical demos (with support from our product team), proposal, negotiation and close. Represent Neuroelectrics at conferences, trade shows and customer sites. Monitor the market — competitors, pricing, trends, funding cycles — and adjust the strategy accordingly. Maintain accurate CRM records and forecasts; report progress against targets to the Sales Director. Work closely with our Marketing and Product Management teams to align messaging, gather customer insights and shape the go-to-market. What do you need At least 3 years of experience, with must have hunter mentality. Proven track record of hitting and exceeding sales targets in the EU market . Bachelor's degree in business, plus a technical or scientific background (or equivalent experience). clinical understanding: knowledge of EEG technology , including routine EEG, Ambulatory EEG, LTM (Long-Term Monitoring), and cEEG in the ICU. Comfortable creating and executing a sales plan, analysing data and reporting on progress. Excellent communication and presentation skills in English. Willingness to travel up to 50–60% within the assigned territory for client site visits and clinical trials. Highly valued Experience selling medical devices, scientific instruments or research equipment. Direct experience with EEG, neurostimulation, neuroimaging or neuroscience-related technology. Established network across neuroscience, neurology, psychiatry, rehabilitation or academic research communities. Clinical or scientific background (neuroscience, biomedical engineering, psychology). You will be the perfect fit if you are/have Passionate about making a difference and gifted with a can-do attitude. Reliable, responsible and respectful. Founder's mindset — urgency, grit, adaptable, willing to push boundaries. Comfortable working autonomously and managing multiple priorities in parallel. Collaborative team player who gets things done. Committed to quality in everything you do. If you join us, you will enjoy: Competitive salary in the sector (according to your experience/skills). 26 vacation days per year + 24th and 31th of December. Fully stocked kitchen (Coffee, organic fruits, snacks, and beverages). Flexible Working Hours. Up to 6 days of working from home per month. Private Health insurance, including dental coverage. Professional development and collaborative environment. Unique opportunity to join our company early with excellent market traction and huge potential to grow Incredible office in Barcelona in Av. Tibidabo. (shower, stunning views of all of Barcelona, etc.) Team Building Events. Neuroelectrics is an equal opportunity organisation. We welcome applications from all qualified candidates regardless of background, identity or beliefs.", "summaryDescription" : "Sales Manager (Medical Device) at Neuroelectrics. Skills: Sales Management, Medical Devices, EEG Technology. Develop Spanish sales plan. Execute Spanish sales plan", "createdAt" : "2026-06-14T06:29:57.364", "lastUpdated" : "2026-06-15T12:04:09.151", "ingestTimestamp" : "2026-06-14T06:29:57.364", "mongoId" : "6a2d58da74d8ee00a0b875d6", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "50k-75k", "hasSalary" : false, "allSkills" : [ "Sales target achievement", "Data analysis", "CRM record maintenance", "Routine EEG", "Ambulatory EEG", "Long-Term Monitoring", "CEEG in ICU", "Grit", "Push boundaries", "Autonomous work", "Manage multiple priorities", "Gets things done", "Committed to quality", "Sales Management", "Medical Devices", "EEG Technology", "Sales plan execution", "Pipeline building", "Deal closure", "Market monitoring", "Strategy adjustment", "Customer insights gathering", "Go-to-market shaping", "Sales plan creation", "EU research landscape", "Clinical landscape", "EEG technology", "Non-invasive brain stimulation", "Epilepsy", "Stroke", "Depression", "Alzheimer's", "Neuroscience", "Neurology", "Psychiatry", "Rehabilitation", "Academic research", "CRM" ], "skillCount" : 38, "jobCategory" : "sales", "jobSubcategory" : "revenue", "seniorityLevel" : "Manager", "dataQualityScore" : 0.8888889, "_score" : 679.7471, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.97 }, { "id" : "68ed10aa70f0b99d58e7b9ea", "title" : "Device Associate, Quality Services, Device Tech Support", "company" : "Amazon Development Centre (India) Private Limited", "industry" : "Operations, IT, Support Engineering, Device Associates, alexa and amazon devices", "salary" : { "min" : 450000.0, "max" : 750000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on the market baseline for an entry-level Device Associate, Quality Services, Device Tech Support role in Chennai, India, with adjustments for the technology industry and company size." }, "location" : "Chennai, Tamil Nadu, IND", "locations" : [ "Chennai, Tamil Nadu, IND" ], "timestamp" : "2026-06-15T09:07:02.654", "fingerprint" : "bd5d20f4a13c651a87d615125b96e4bd2cce3732a73f8781604f69240a44904e", "source" : "amazon", "language" : "en", "applyUrl" : "https://account.amazon.com/jobs/3105248/apply", "externalId" : "b161c2fb-79e3-434b-a8bb-af88a26d14d9", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Chennai", "state" : "Tamil Nadu", "country" : "India", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "13.0836939,80.2701860" } ], "locationText" : "Chennai, Tamil Nadu, India", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "coreResponsibilities" : "Execute test plans, Execute test cases, Create test data, Report results, Understand project functionality, Stay connected with requirements, Stay connected with documentation, Look for gaps in test cases, Look beyond test cases for issues, Execute processes to test product changes, Backtrack bugs, Backtrack issues, Perform root cause analysis of bugs, Perform root cause analysis of issues, Execute regression cases, Raise bugs, Support ad-hoc requests, Interact with QA for new features, Support first pass, Support bug repro, Contribute ideas, Take part in implementing ideas", "teamCollaboration" : "Interacting with QA", "domainKnowledge" : "E-reader devices", "domainList" : [ "e-reader-devices" ], "domainSpecificKnowledge" : [ "E-reader devices" ], "problemSolvingSkills" : "Root cause analysis", "qualificationsBasic" : "Bachelor's degree, Knowledge of QA methodology, Knowledge of QA tools", "qualificationsPreferred" : "Good Communication, Testing Knowledge, Good Analytical Skill", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "At this role the associate gets a chance to work on multiple generations of E-reader devices and will directly contribute to the high quality of the devices. Key job responsibilities - Execute test plans & test cases, creating test data, and reporting results in a timely, clear, and concise manner. - Should have understanding of the functionality of the project/product. Should have the ability to stay connected with changing requirements and documentation. - Should be able to actively look for gaps in test cases and look beyond test cases for issues/bugs. - Should execute processes to thoroughly test product changes. - Should have the ability to backtrack and do a root cause analysis of bugs/issues. A day in the life A typical day involves executing regression cases , raising bugs, supporting ad-hoc requests etc. Also involves interacting with QA for new features, supporting first pass and bug repro. Contributing ideas and take part in implementing them About the team Highly energetic and fun loving team with great flexibility. Team contributes to multiple aspect of the quality of E-reader devices. Handles multiple parallel releases successfully. Basic Qualifications: - Bachelor's degree - Knowledge of QA methodology and tools Preferred Qualifications: - Good Communication - Testing Knowledge - Good Analytical Skill 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" : "Device Associate, Quality Services, Device Tech Support at Amazon Development Centre (India) Private Limited. Execute test plans. Execute test cases", "postedDate" : "2026-06-14T07:38:01.235", "createdAt" : "2026-06-14T07:38:01.235", "lastUpdated" : "2026-06-15T09:07:02.654", "ingestTimestamp" : "2026-06-14T07:38:01.235", "mongoId" : "68ed10aa70f0b99d58e7b9ea", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.com/jobs/3105248/apply", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "E-reader devices" ], "skillCount" : 1, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Entry", "dataQualityScore" : 0.8888889, "_score" : 678.83124, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.95 }, { "id" : "68c2e42cf8b1b0376634c71a", "title" : "Device Quality Manager", "company" : "Amazon Corporate Services Vietnam Company Limited", "industry" : "Systems, Quality, Security Engineering, Hardware Development, alexa and amazon devices", "salary" : { "min" : 1.05E9, "max" : 1.575E9, "currency" : "VND", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Device Quality Manager in Hanoi, Vietnam, adjusted for industry and company size." }, "location" : "Hanoi, VNM", "locations" : [ "Hanoi, VNM" ], "certifications" : [ "Six Sigma Greenlack belt", "ASQ CQE/M/A" ], "timestamp" : "2026-06-15T02:47:32.195", "fingerprint" : "860f28e635c481c66528acbcad785a514e71d32faa772a2393bf64e627435738", "source" : "amazon", "language" : "en", "applyUrl" : "https://account.amazon.com/jobs/3076132/apply", "externalId" : "8dfd305e-4264-47c2-a963-cca148ec235f", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Hanoi", "country" : "Vietnam", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "21.0283334,105.8540410" } ], "locationText" : "Hanoi, Vietnam", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 7, "experienceLevel" : "Manager", "professionalSkills" : [ "Quality management", "Process improvement", "Data analysis", "Failure analysis", "Root cause determination", "Corrective action", "Customer use cases", "Product development", "Factory audits", "Shipment readiness assessment", "Production performance monitoring", "Quality health reporting", "Continuous improvement", "Quality escapes", "Problem solving activities", "Issue resolution" ], "hardSkillsList" : [ "DMAIC", "Lean", "Six Sigma" ], "softSkillsList" : [ "Sense of urgency", "Leadership" ], "hardSkills" : [ { "name" : "DMAIC", "level" : "intermediate" }, { "name" : "Lean", "level" : "intermediate" }, { "name" : "Six Sigma", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Sense of urgency" }, { "name" : "Leadership" } ], "majorSkills" : "Device Quality Management, Manufacturing Quality, Process Audits", "majorSkillsList" : [ "Device Quality Management", "Manufacturing Quality", "Process Audits" ], "coreResponsibilities" : "Develop out of box audit process, Work with contract manufacturer, Validate product HW/SW functionality, Validate product cosmetics characteristics, Lead regional team, Assess customer shipment readiness, Own factory quality, Monitor production performance, Conduct factory audits, Partner with Amazonian in factories, Lead investigation, Lead failure analysis, Determine root cause, Implement closed loop corrective action, Lead factory quality lessons learned, Institute remedies, Provide production quality health report, Drive continuous improvement, Initiate quality pre-alert, Lead cross-functional teams, Provide effective issue resolution", "teamCollaboration" : "Cross-functional product core team; Fellow Amazonian in factories; Cross-functional teams", "domainKnowledge" : "Consumer electronics; Electronic assembly processes", "domainList" : [ "consumer-electronics", "electronic-assembly-processes" ], "domainSpecificKnowledge" : [ "Consumer electronics", "Electronic assembly processes" ], "communicationSkills" : "Oral communication; Written communication", "problemSolvingSkills" : "Problem Solver; Data analysis; Methodical approach; Failure analysis; Root cause determination", "qualificationsBasic" : "BSMESIE/BSEE or related Engineering degree, 7+ years working experience, 5+ years manufacturing quality, Good understanding electronic assembly, Problem Solver, Lean / Six Sigma tools, Failure Mode & Effects Analysis, Design of Experiments, Measurement System Analysis, Analysis of Variance, Hypothesis Testing, Value Stream Mapping, Pareto Charts, Gage Repeatability & Reproducibility, Cpk, Technical knowledge process audits, Formulating plans quality improvements, Self-motivated/self-directed, Manage multiple work streams", "qualificationsPreferred" : "MSME/MSIE/MSEE, Six Sigma Greenlack belt, ASQ CQE/M/A certifications, Create and innovate quality deliverables, Advanced understanding quality tools, Ability to influence others, Interact at all levels", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "The Device Quality Manager (DQM) is responsible for ensuring that Amazon products are manufactured for quality. During the new product development (NPI), the DQM will develop an out of box audit (OBA) process for factory production based on critical to customer use cases of the product. With guidance from cross-functional product core team, DQM will work with the contract manufacturer in delivering a robust OBA process that validates product HW/SW functionality and product cosmetics characteristics to ensure that Lab126 delivers high quality products to customers. DQM will also lead small regional team to assess customer shipment readiness from Southeast Asia manufacturing factories. The DQM will also own factory quality in the sustaining phase of the product. The successful candidate will monitor production performance against established quality goals by conducting regular factory audits, partnering with fellow Amazonian in factories to lead full investigation and failure analysis leading to root cause determination and subsequent closed loop corrective action. DQM must possess a high sense of urgency when managing critical issues. DQM will lead factory quality lessons learned and institutes remedies to prevent re-occurrence of such issues. In addition, the DQM will provide production quality health report to management in sustaining phase and drive continuous improvement in all aspects of the job. DQM will also initiate quality pre-alert for any quality escapes from the factory impacting customers and lead cross-functional teams in problem solving activities to provide effective issue resolution. Basic Qualifications: • Minimum of a BSME/BSIE/BSEE or related Engineering degree • Preferred 7+ years of working experience in engineering and/or quality role with 5+ years in a manufacturing quality environment. • Good understanding of electronic assembly processes mostly on consumer electronics. • Problem Solver - Deliver solutions to complex problems through in-depth data analysis and forensics, using methodical approach such as DMAIC along with experience, innovation and judgment to make decisions that may be based on partial information • Solid understanding and demonstrated success with practical applications of Lean / Six Sigma tools such as Failure Mode & Effects Analysis, Design of Experiments, Measurement System Analysis, Analysis of Variance, Hypothesis Testing, Value Stream Mapping, Pareto Charts, Gage Repeatability & Reproducibility, Cpk. • Technical knowledge of conducting process audits and formulating plans to drive continual quality improvements within the factory operations • Must be self-motivated/self-directed, is able to manage multiple work streams simultaneously and flawlessly. • Excellent oral and written communication skills in Vietnamese Preferred Qualifications: • MSME/MSIE/MSEE • Six Sigma Green/Black belt, ASQ CQE/M/A certifications are highly desired. • Ability to create and innovate quality deliverables/processes during new product development and sustaining program management • Advanced understanding and deployment of quality tools • Ability to influence others and interact at all levels within the organization 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" : "Device Quality Manager at Amazon Corporate Services Vietnam Company Limited. Skills: Device Quality Management, Manufacturing Quality, Process Audits. Develop out of box audit process. Work with contract manufacturer", "postedDate" : "2026-06-13T06:43:16.481", "createdAt" : "2026-06-13T06:43:16.481", "lastUpdated" : "2026-06-15T02:47:32.195", "ingestTimestamp" : "2026-06-13T06:43:16.481", "mongoId" : "68c2e42cf8b1b0376634c71a", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.com/jobs/3076132/apply", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "DMAIC", "Lean", "Six Sigma", "Sense of urgency", "Leadership", "Device Quality Management", "Manufacturing Quality", "Process Audits", "Quality management", "Process improvement", "Data analysis", "Failure analysis", "Root cause determination", "Corrective action", "Customer use cases", "Product development", "Factory audits", "Shipment readiness assessment", "Production performance monitoring", "Quality health reporting", "Continuous improvement", "Quality escapes", "Problem solving activities", "Issue resolution", "Consumer electronics", "Electronic assembly processes", "Six Sigma Greenlack belt", "ASQ CQE/M/A" ], "skillCount" : 28, "jobCategory" : "engineering", "dataQualityScore" : 1.0, "_score" : 667.5121, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a2c7d3274d8ee00a094f3d1", "title" : "Senior Internal Auditor", "company" : "Braze", "industry" : "SaaS", "salary" : { "min" : 145000.0, "max" : 205000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Senior Internal Auditor in New York, adjusted for SaaS industry and company size." }, "location" : "New York City", "locations" : [ "New York City" ], "certifications" : [ "CPA", "CIA", "CISA" ], "timestamp" : "2026-06-15T11:23:07.330", "fingerprint" : "038034349b9e79298e16a70b4deb071e71ce8a1610438b28aec8fb4a35ce8cbc", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://boards.greenhouse.io/braze/jobs/7992841?gh_jid=7992841", "externalId" : "7992841", "industryFunction" : { }, "structuredLocations" : [ { "city" : "New York", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.7127281,-74.0060152" } ], "locationText" : "New York, New York, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Data analysis, SQL", "professionalSkills" : [ "Risk management", "Internal controls", "Audit analytics", "Process improvement" ], "hardSkillsList" : [ "SOX compliance", "Operational audits", "Financial audits", "Technology audits", "Risk assessments", "Control testing", "Remediation validation", "Data analytics", "Continuous monitoring", "Automation" ], "softSkillsList" : [ "Intellectually curious", "Analytical" ], "hardSkills" : [ { "name" : "SOX compliance", "level" : "intermediate" }, { "name" : "Operational audits", "level" : "intermediate" }, { "name" : "Financial audits", "level" : "intermediate" }, { "name" : "Technology audits", "level" : "intermediate" }, { "name" : "Risk assessments", "level" : "intermediate" }, { "name" : "Control testing", "level" : "intermediate" }, { "name" : "Remediation validation", "level" : "intermediate" }, { "name" : "Data analytics", "level" : "intermediate" }, { "name" : "Continuous monitoring", "level" : "intermediate" }, { "name" : "Automation", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Intellectually curious" }, { "name" : "Analytical" } ], "majorSkills" : "SOX compliance, Internal controls, Risk management, Data analytics", "majorSkillsList" : [ "SOX compliance", "Internal controls", "Risk management", "Data analytics" ], "coreResponsibilities" : "Perform SOX testing activities, Coordinate with internal stakeholders, Monitor and validate remediation activities, Assist in execution of audits, Support audit planning activities, Assess business processes, Support Enterprise Risk Management activities, Leverage data analytics and audit tools, Support continuous monitoring initiatives, Leverage tools such as Jira, Support preparation in audit reports, Facilitate meetings, Contribute to continuous improvement", "teamCollaboration" : "Partner with stakeholders; Coordinate with external auditors; Communicate audit results", "domainKnowledge" : "SOX compliance; Enterprise Risk Management; Subscription revenue; Professional services revenue", "domainList" : [ "sox-compliance", "enterprise-risk-management", "subscription-revenue", "professional-services-revenue" ], "domainSpecificKnowledge" : [ "SOX compliance", "Enterprise Risk Management", "Subscription revenue", "Professional services revenue" ], "toolProficiency" : [ "Jira", "Workiva", "Data analytics platforms" ], "communicationSkills" : "Executive-ready communications; Audit reports; Presentations", "documentationSkills" : "Documentation updates; Audit workpapers", "continuousLearning" : "Learning platforms; Yearly learning stipend", "problemSolvingSkills" : "Identify control gaps; Identify process improvement opportunities", "qualificationsBasic" : "B. S. in Accounting, 3 years minimum relevant experience, Software/SaaS industry experience, Demonstrated experience with Sarbanes-Oxley compliance, Demonstrated experience with internal controls, Demonstrated experience with risk management, Skills in data analysis, Writing SQL queries, Understanding database structures, Extracting actionable insights", "qualificationsPreferred" : "Professional certification such as CPA, Professional certification such as CIA, Professional certification such as CISA, Public Accounting experience, IT General Controls experience, Experience with subscription and professional services revenue", "remoteFriendly" : false, "rawDescription" : "At Braze, we have found our people. We’re a genuinely approachable, exceptionally kind, and intensely passionate crew. We seek to ignite that passion by setting high standards, championing teamwork, and creating work-life harmony as we collectively navigate rapid growth on a global scale while striving for greater equity and opportunity – inside and outside our organization. To flourish here, you must be prepared to set a high bar for yourself and those around you. There is always a way to contribute: Acting with autonomy, having accountability and being open to new perspectives are essential to our continued success. Our deep curiosity to learn and our eagerness to share diverse passions with others gives us balance and injects a one-of-a-kind vibrancy into our culture. If you are driven to solve exhilarating challenges and have a bias toward action in the face of change, you will be empowered to make a real impact here, with a sharp and passionate team at your back. If Braze sounds like a place where you can thrive, we can’t wait to meet you. What We’re Looking For We are seeking a Senior Internal Auditor to support and help evolve our Internal Audit function. This role is ideal for a hands-on audit professional who is eager to contribute across SOX compliance, operational audits, enterprise risk management, and audit analytics within a fast-paced, high-growth SaaS environment. Reporting to Internal Audit leadership, you will partner with stakeholders across Technology, Engineering, Finance, Legal, Security, and other business functions to evaluate risk, strengthen internal controls, and identify opportunities to improve business processes. You will play a key role in executing risk-based audit activities while helping the team leverage automation, data analytics, and continuous monitoring techniques to enhance audit effectiveness and efficiency. The ideal candidate has experience with SOX compliance, internal controls, and audit execution within a public company, public accounting, or technology-focused environment. You are intellectually curious, analytical, highly collaborative, and comfortable operating in an Agile environment. What You’ll Do Perform SOX testing activities, including walkthroughs, control testing, documentation updates, deficiency tracking, and remediation validation. Coordinate with internal stakeholders, external auditors, and co-source providers to facilitate audit execution and evidence collection. Monitor and validate remediation activities to ensure timely resolution of identified issues and control deficiencies. Assist in the execution of risk-based operational, compliance, financial, and technology audits from planning through reporting. Support audit planning activities by conducting risk assessments, gathering information, and preparing audit workpapers. Assess business processes, automated controls, and system implementations to identify control gaps and process improvement opportunities. Support quarterly Enterprise Risk Management (ERM) activities, including risk identification, risk scoring, mitigation tracking, and reporting. Leverage data analytics and audit tools to enhance testing effectiveness, identify trends, and provide actionable insights to stakeholders. Support continuous monitoring, automation, and AI-driven audit initiatives to improve audit coverage and efficiency. Leverage tools such as Jira, Workiva, and data analytics platforms to enhance audit execution, documentation, and reporting processes. Support preparation in clear and concise audit reports, presentations, and executive-ready communications that summarize risks, observations, and recommendations. Facilitate meetings, document key discussions and action items, and effectively communicate audit results to stakeholders. Contribute to the continuous improvement of Internal Audit methodologies, standards, and operational practices. Who You Are To excel in this role, you will need a combination of technical expertise, interpersonal skills, and a commitment to upholding regulatory standards. Key qualifications and attributes we're looking for include: B. S. in Accounting, Finance, Information Systems or related area Professional certification such as CPA, CIA or CISA 3 years minimum relevant experience, including Public Accounting or industry experience Software/SaaS or Technology industry experience with subscription and professional services revenue Demonstrated experience with Sarbanes-Oxley compliance, internal controls (ideally, both financial process and IT General Controls), and risk management within a corporate environment. Strong skills in data analysis, including writing SQL queries, understanding database structures, and extracting actionable insights from complex datasets. Proven track record of supporting audits, note-taking, and facilitating meetings, ideally in international settings. Strong leadership skills, high EQ and proactive problem solving approach Ability to collaborate with onshore and offshore team(s) Experience using Workiva GRC platform is a plus Experience with agile project management methodologies a plus For candidates based in the United States, the pay range for this position at the start of employment is expected to be between $88,000 and $131,000/year, with an expected On Target Earnings (OTE) between $98,000 and $146,000/year (including bonus or commission). Your exact offer may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition to cash compensation, this role qualifies for a comprehensive Total Rewards package that includes equity grants of restricted stock (RSUs) so that you will own a piece of our company. WHAT WE OFFER Braze benefits vary by location, and we encourage you to review our specific benefits offerings for each country here. More details on benefits plans will be provided if you receive an offer of employment. From offering comprehensive benefits to fostering hybrid ways of working, we’ve got you covered so you can prioritize work-life harmony. Braze offers benefits such as: Competitive compensation that may include equity Retirement and Employee Stock Purchase Plans Flexible paid time off Comprehensive benefit plans covering medical, dental, vision, life, and disability Family services that include fertility benefits and equal paid parental leave Professional development supported by formal career pathing, learning platforms, and a yearly learning stipend A curated in-office employee experience, designed to foster community, team connections, and innovation Opportunities to give back to your community, including an annual company-wide Volunteer Week and donation matching Employee Resource Groups that provide supportive communities within Braze Collaborative, transparent, and fun culture recognized as a Great Place to Work® ABOUT BRAZE Braze is the leading customer engagement platform that empowers brands to Be Absolutely Engaging™. Braze helps brands deliver great customer experiences that drive value both for consumers and for their businesses. Built on a foundation of composable intelligence, BrazeAI™ allows marketers to combine and activate AI agents, models, and features at every touchpoint throughout the Braze Customer Engagement Platform for smarter, faster, and more meaningful customer engagement. From cross-channel messaging and journey orchestration to Al-powered decisioning and optimization, Braze enables companies to turn action into interaction through autonomous, 1:1 personalized experiences. The company has been consistently recognized as a Leader in marketing technology by industry analysts, and was named a G2 “Best of Marketing and Digital Advertising Software Product” in 2026. Braze was also named a 2026 Best Places to Work by Built In, a 2025 America’s Greenest Companies by Newsweek, and a 2025 Fortune Best Workplace in Technology™ by Great Place To Work®. Braze is also proudly certified as a Great Place to Work® in the U.S., the UK, Australia, and Singapore. The company is headquartered in New York with offices in Austin, Berlin, Bucharest, Chicago, Dubai, Jakarta, London, Paris, San Francisco, São Paulo, Singapore, Seoul, Sydney and Tokyo. BRAZE IS AN EQUAL OPPORTUNITY EMPLOYER At Braze, we strive to create equitable growth and opportunities inside and outside the organization. Building meaningful connections is at the heart of everything we do, and that includes our recruiting practices. We're committed to offering all candidates a fair, accessible, and inclusive experience – regardless of age, color, disability, gender identity, marital status, maternity, national origin, pregnancy, race, religion, sex, sexual orientation, or status as a protected veteran. When applying and interviewing with Braze, we want you to feel comfortable showcasing what makes you you. We know that sometimes different circumstances can lead talented people to hesitate to apply for a role unless they meet 100% of the criteria. If this sounds familiar, we encourage you to apply, as we’d love to meet you. Please see our Candidate Privacy Policy for more information on how Braze processes your personal information during the recruitment process and, if applicable based on your location, how you can exercise any privacy rights.", "summaryDescription" : "Senior Internal Auditor at Braze. Skills: SOX compliance, Internal controls, Risk management, Data analytics. Perform SOX testing activities. Coordinate with internal stakeholders", "postedDate" : "2026-06-14T09:00:02.420", "createdAt" : "2026-06-14T09:00:02.420", "lastUpdated" : "2026-06-15T11:23:07.330", "ingestTimestamp" : "2026-06-14T09:00:02.420", "mongoId" : "6a2c7d3274d8ee00a094f3d1", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 145000, "salaryAnnualMax" : 205000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "SOX compliance", "Operational audits", "Financial audits", "Technology audits", "Risk assessments", "Control testing", "Remediation validation", "Data analytics", "Continuous monitoring", "Automation", "Intellectually curious", "Analytical", "Internal controls", "Risk management", "Audit analytics", "Process improvement", "Enterprise Risk Management", "Subscription revenue", "Professional services revenue", "CPA", "CIA", "CISA", "Jira", "Workiva", "Data analytics platforms" ], "skillCount" : 25, "jobCategory" : "finance", "jobSubcategory" : "accounting", "seniorityLevel" : "Senior", "dataQualityScore" : 1.0, "_score" : 657.25366, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "SaaS", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2eb32874d8ee00a0e7dd2c", "title" : "Service Quality Auditor", "company" : "Citi", "salary" : { "min" : 1500000.0, "max" : 2500000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Senior Service Quality Auditor in Banking at Citi in DLF CYBERCITY, India, adjusted for seniority and company size." }, "location" : "DLF CYBERCITY 12B", "locations" : [ "DLF CYBERCITY 12B", "India" ], "timestamp" : "2026-06-16T04:56:07.950", "fingerprint" : "36abc1b115f2f4c52e4c68999ee64daa5e3448001d4eb5478906853295a62797", "source" : "workday", "language" : "en", "applyUrl" : "https://citi.wd5.myworkdayjobs.com/2/job/DLF-CYBERCITY-12B/Service-Quality-Auditor_26970414-1", "externalId" : "26970414", "industryFunction" : { }, "locationPoint" : "-20.24494,57.49163", "structuredLocations" : [ { "city" : "DLF CYBERCITY 12B", "country" : "India", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "17.4470914,78.3557479" } ], "locationText" : "DLF CYBERCITY 12B, India", "employmentType" : "FULL_TIME", "experienceMinYears" : 7, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "coreResponsibilities" : "Manage operational processes, Monitor operational performance, Identify process improvements, Implement process changes, Coordinate with cross-functional teams, Manage vendor relationships, Track operational metrics, Report on operational status", "teamCollaboration" : "Cross-functional teams; Vendor management", "domainKnowledge" : "Process management; Operational metrics; Resource planning; Continuous improvement", "domainList" : [ "process-management", "operational-metrics", "resource-planning", "continuous-improvement" ], "domainSpecificKnowledge" : [ "Process management", "Operational metrics", "Resource planning", "Continuous improvement" ], "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "The Ops Support Specialist position responsible for providing operations support services, including but not limited to; record/documentation maintenance, storage & retrieval of records, account maintenance, imaging and the opening of accounts in coordination with the Operations - Core Team. Additionally, the Ops Support Specialist serves as the liaison between operations staff, relationship managers, project managers, custodians and clients. The overall objective of this role is to provide day-to-day operations support in alignment with Citi operations support infrastructure and processes. **_Responsibilities:_** * Follow established procedures to complete complex assignments and resolve problems that require in-depth investigation or research * Provide team assistance, including serving as subject matter expert, leading special projects, training new hires within work unit, providing daily guidance to lower level employees, and allocation of work, as needed * Conduct basic analysis and research as well as workflow management * Support an expansive array of products and services * Communicate pertinent information to senior managers and support activities that help mitigate organizational loss or impact, as needed * Appropriately assess risk when business decisions are made, demonstrating particular consideration for the firm's reputation and safeguarding Citigroup, its clients and assets, by driving compliance with applicable laws, rules and regulations, adhering to Policy, applying sound ethical judgment regarding personal behavior, conduct and business practices, and escalating, managing and reporting control issues with transparency. **_Qualifications:_** * 7+ yrs of relevant experience preferred * Experience working in a business office or operational environment * Production-focused agents responsible for ensuring the efficiency and accuracy of SQ Audits. * Executes SQ audits, identifies and documents defects, and contributes to the continuous improvement of quality processes. * Demonstrates technical and administrative expertise * Proficient in executing manual and automated SQ test cases and performing root cause analysis for identified issues. * Familiarity with Optimizer work bench, Debt Manager tool, and utilizing version control systems. Demonstrates a strong aptitude for detail and commitment to delivering high-quality audit results. * Consistently demonstrates attention to detail * Demonstrated knowledge of activities, policies, and procedures of a basic work area ** _Education:_** * Bachelor’s degree/University degree or equivalent experience This job description provides a high-level review of the types of work performed. Other job-related duties may be assigned as required. ### \\------------------------------------------------------ ## **Job Family Group:** Operations - Core \\------------------------------------------------------ ## **Job Family:** Operations Support \\------------------------------------------------------ ## **Time Type:** Full time \\------------------------------------------------------ ## **Most Relevant Skills** Please see the requirements listed above. \\------------------------------------------------------ ## **Other Relevant Skills** Automation Testing, Data Analysis, Data Management, Manual Testing, Operational Process Improvements, Service Quality Assurance. \\------------------------------------------------------ _Citi is an equal opportunity employer, and qualified candidates will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other characteristic protected by law._ __ _If you are a person with a disability and need a reasonable accommodation to use our search tools and/or apply for a career opportunity review_ _[Accessibility at Citi](https://www.citigroup.com/citi/accessibility/application-accessibility.htm)._ _View Citi’s[EEO Policy Statement](https://www.citigroup.com/global/eeo-aa-policy) and the [Know Your Rights](https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12ScreenRdr.pdf) poster._", "summaryDescription" : "Service Quality Auditor at Citi. Manage operational processes. Monitor operational performance", "postedDate" : "2026-06-12T21:23:28.443", "createdAt" : "2026-06-14T21:23:28.425", "lastUpdated" : "2026-06-16T04:56:07.950", "ingestTimestamp" : "2026-06-14T21:23:28.425", "mongoId" : "6a2eb32874d8ee00a0e7dd2c", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://citi.wd5.myworkdayjobs.com/2/job/DLF-CYBERCITY-12B/Service-Quality-Auditor_26970414-1", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Process management", "Operational metrics", "Resource planning", "Continuous improvement" ], "skillCount" : 4, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "mid", "dataQualityScore" : 1.0, "_score" : 647.2327, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Banking", "llmIndustryConfidence" : 0.95 }, { "id" : "69f9eb6b4c40e2acd13051eb", "title" : "Medical Coding Auditor - Profee Coding", "company" : "AOSP", "industry" : "Finance Accounting, Finance/Planning, healthcare", "salary" : { "min" : 750000.0, "max" : 1200000.0, "currency" : "PHP", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Medical Coding Auditor in Pasay City, Philippines, adjusted for the Healthcare industry." }, "location" : "Pasay City, National Capital Region, PHL", "locations" : [ "Pasay City, National Capital Region, PHL" ], "certifications" : [ "CPC certification", "CCS certification", "CRC license" ], "timestamp" : "2026-06-15T02:06:12.768", "fingerprint" : "f957fb7393ba7893097b4fd763395231f9ea02fecd0d8ec8eded866a4d54eea4", "source" : "amazon", "language" : "en", "applyUrl" : "https://account.amazon.jobs/jobs/10411182/apply", "externalId" : "b9532890-6d26-4e97-8a98-32438f71cd12", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Pasay City", "state" : "National Capital Region", "country" : "Philippines", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "14.5436995,120.9946503" } ], "locationText" : "Pasay City, National Capital Region, Philippines", "employmentType" : "FULL_TIME", "professionalSkills" : [ "Process excellence", "Financial improvement", "Operations accounting", "Operations excellence", "Risk Adjustment", "Coding", "Documentation requirements" ], "hardSkillsList" : [ "Medical coding", "Quality analysis", "Process training", "Audit observations", "Root cause analysis", "Coding guidelines", "Risk adjustment guidance", "Chart reviews", "HCC risk adjustment" ], "softSkillsList" : [ "Accountability", "Setting high standards", "Raising the bar", "Driving results", "Attention to detail" ], "hardSkills" : [ { "name" : "Medical coding", "level" : "intermediate" }, { "name" : "Quality analysis", "level" : "intermediate" }, { "name" : "Process training", "level" : "intermediate" }, { "name" : "Audit observations", "level" : "intermediate" }, { "name" : "Root cause analysis", "level" : "intermediate" }, { "name" : "Coding guidelines", "level" : "intermediate" }, { "name" : "Risk adjustment guidance", "level" : "intermediate" }, { "name" : "Chart reviews", "level" : "intermediate" }, { "name" : "HCC risk adjustment", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Accountability" }, { "name" : "Setting high standards" }, { "name" : "Raising the bar" }, { "name" : "Driving results" }, { "name" : "Attention to detail" } ], "majorSkills" : "Medical coding, Quality analysis, Risk adjustment", "majorSkillsList" : [ "Medical coding", "Quality analysis", "Risk adjustment" ], "coreResponsibilities" : "Lead training initiatives, Create training materials, Conduct training needs analysis, Conduct process trainings, Supplement training topics, Conduct spot checks monthly, Provide progress reports, Discuss audit results monthly, Analyze trends, Analyze root causes, Participate in special projects, Provide recommendations for quality opportunities, Provide recommendations for action plans, Manage coding projects, Ensure project deliverables, Assign ICD-10-CM codes, Assign CPT codes, Assign other relevant codes, Review email requests, Complete email requests, Work collaboratively with Medicare Risk Operations team", "teamCollaboration" : "Leadership teams; Medicare Risk Operations team", "projectManagementSkills" : [ "Managing multiple projects" ], "domainKnowledge" : "Health systems operations; Reimbursement methodologies; Coding conventions; HCC risk adjustment; CPT coding guidelines; ICD-10-CM coding guidelines; AHA Coding Clinic Guidance; CMS Risk Adjustment guidance", "domainList" : [ "health-systems-operations", "reimbursement-methodologies", "coding-conventions", "hcc-risk-adjustment", "cpt-coding-guidelines", "icd-10-cm-coding-guidelines", "aha-coding-clinic-guidance", "cms-risk-adjustment-guidance" ], "domainSpecificKnowledge" : [ "Health systems operations", "Reimbursement methodologies", "Coding conventions", "HCC risk adjustment", "CPT coding guidelines", "ICD-10-CM coding guidelines", "AHA Coding Clinic Guidance", "CMS Risk Adjustment guidance" ], "toolProficiency" : [ "Microsoft Suite", "Google Suite" ], "communicationSkills" : "Written communication; Verbal communication", "documentationSkills" : "Documentation requirements", "problemSolvingSkills" : "Problem-solving skills; Analytical skills", "qualificationsBasic" : "Completed Bachelor's Degree, CPC certification through AAPC, CCS certification through AHIMA, 1+ year outpatient coder, 1+ year risk adjustment coder, Knowledge of health systems operations, Understanding of reimbursement methodologies, Understanding of coding conventions, Perform accurate chart reviews, Complete chart reviews for HCC risk Adjustment, Advanced knowledge of HCC risk adjustment, Advanced knowledge of coding, Advanced knowledge of documentation requirements, Experience in a coding production environment", "qualificationsPreferred" : "1+ year outpatient auditor, 1+ year risk adjustment auditor, 1+ year experience in Medicare, 1+ year experience in Medicare Advantage, CRC license within one year, Experience in Microsoft Suite, Experience in Google Suite, Works efficiently within a team, Adaptable to shifting priorities, Willingness to meet client needs, Willingness to meet team needs, Complies with confidentiality policies, Complies with security policies, Ability to work independently, Meet quality of work expectations, Meet workload expectations, Manage multiple projects", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "The Finance Operations organization works with every part of Amazon to provide operations accounting and operations excellence services with the highest level of controllership at the lowest cost to the company. We provide the backbone systems and operational processes which completely, accurately, and validly pay Amazon’s suppliers, invoice our customers and report financial results. Amazon is quickly building the Finance Operations capabilities in the healthcare industry by creating the Healthcare Finance Operations Services. As part of the Amazon Healthcare Global Finance Operations Services team, you will find yourself working with exceptionally talented and determined people committed to driving financial improvement, scalability, and process excellence. To support the growth of Amazon HealthCare, this candidate must possess a strong passion for accountability, setting high standards, raising the bar, and driving results through constant focus on improving existing and future state operations, systems, and processes in collaboration with Management. As we continue to grow and scale our ability to provide innovative primary care across the country, the teams that support this critical work are growing as well. Amazon Healthcare is seeking to hire Medical Coder - Quality Analyst for the Revenue Cycle team. As a member of the Revenue Cycle team, the Medical Coder - Quality Analyst will be leading Manila's One Medical’s Coding's Quality Program. This position is office-based in Pasay City. Key job responsibilities Key job responsibilities as a Quality Analyst (but are not limited to): • Lead training initiatives such as training materials creation and training needs analysis. • Conduct process trainings via leading or supplementing training topics for specific processes. • Auditor will have to conduct spot checks on a monthly basis based on existing quality parameters. • Provide progress reports to leadership teams regarding quality results and action items on quality misses. • Discuss results of audits on a monthly basis. • Analyze and monitor trends and root causes on audit observations. • Participate in special projects as requested by Leadership. • Provide inputs or recommendations for quality opportunities and action plans. Key job responsibilities as a Coding: • Managing multiple coding related projects and ensuring deliverables are up to One Medical standards while being turned around in an acceptable time frame. • Remaining current on CPT, ICD-10-CM coding guidelines, AHA Coding Clinic Guidance and CMS Risk Adjustment guidance (as needed). • Assign appropriate ICD-10-CM, CPT, and other relevant codes to office visits, procedures, and diagnoses in a production environment. • Responsible for the review and completion of email requests in a timely manner as well as reviewing. • Work collaboratively with the Medicare Risk Operations team to ensure positive program outcomes. Basic Qualifications: - Completed Bachelor's Degree - CPC certification through AAPC and/or CCS certification through AHIMA is required - 1+ year as an outpatient and/or risk adjustment coder - Demonstrates knowledge of health systems operations, including an understanding of reimbursement methodologies and coding conventions - Demonstrates the ability to perform accurate and complete chart reviews for HCC risk Adjustment - Possess advanced knowledge and understanding of HCC risk adjustment, coding, and documentation requirements. - Previous experience in a coding production environment. Preferred Qualifications: - 1+ year as an outpatient and/or risk adjustment auditor - 1+ year experience in Medicare/Medicare Advantage - A CRC license must be obtained within one year of hire (to be sponsored) - Must have strong experience in Microsoft or Google Suite in spreadsheets and PowerPoint - Works effectively and efficiently within a team environment. - Adaptable to shifting priorities and demonstrates willingness to do what it takes to meet client and team needs. - Complies with policies and procedures for the confidentiality of all patient records and the security of systems. - Ability to work independently and meet quality of work and workload expectations - Ability to manage multiple projects • Strong written, verbal, communication, and attention to detail skills. - Strong organizational, analytical, problem-solving, and time management skills. 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" : "Medical Coding Auditor - Profee Coding at AOSP. Skills: Medical coding, Quality analysis, Risk adjustment. Lead training initiatives. Create training materials", "postedDate" : "2026-06-13T15:48:50.212", "createdAt" : "2026-06-13T15:48:50.212", "lastUpdated" : "2026-06-15T02:06:12.768", "ingestTimestamp" : "2026-06-13T15:48:50.212", "mongoId" : "69f9eb6b4c40e2acd13051eb", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.jobs/jobs/10411182/apply", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Medical coding", "Quality analysis", "Process training", "Audit observations", "Root cause analysis", "Coding guidelines", "Risk adjustment guidance", "Chart reviews", "HCC risk adjustment", "Accountability", "Setting high standards", "Raising the bar", "Driving results", "Attention to detail", "Risk adjustment", "Process excellence", "Financial improvement", "Operations accounting", "Operations excellence", "Risk Adjustment", "Coding", "Documentation requirements", "Managing multiple projects", "Health systems operations", "Reimbursement methodologies", "Coding conventions", "CPT coding guidelines", "ICD-10-CM coding guidelines", "AHA Coding Clinic Guidance", "CMS Risk Adjustment guidance", "CPC certification", "CCS certification", "CRC license", "Microsoft Suite", "Google Suite" ], "skillCount" : 35, "jobCategory" : "sales", "dataQualityScore" : 0.8888889, "_score" : 646.3655, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "id" : "6a306d86f292fd229cfd8e7c", "title" : "FSQ Auditor", "company" : "Jack Link's Protein Snacks", "industry" : "Consumer Goods", "salary" : { "min" : 75000.0, "max" : 105000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level FSQ Auditor in Minong, Wisconsin, adjusted for the Food & Beverage industry." }, "location" : "Minong, WI, United States", "locations" : [ "Minong", "WI", "United States" ], "timestamp" : "2026-06-16T09:42:22.905", "fingerprint" : "ff793e3594df2084cf88b42a42859c19279aa42d0b1f03951fe2f23ced81d545", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/JackLinksProteinSnacks/744000132287174-fsq-auditor", "externalId" : "744000132287174", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Minong", "state" : "Wisconsin", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "46.1003414,-91.8238136" } ], "locationText" : "Minong, Wisconsin, United States", "employmentType" : "FULL_TIME", "experienceLevel" : "not-applicable", "remoteFriendly" : false, "rawDescription" : "At Link Snacks , we show up hungry, roll up our sleeves, plaid or otherwise, and dive straight into the hard work. We don’t hide from challenges; we hunt them down. We push harder, move faster, and take the kinds of big swings that built this business in the North Woods of Wisconsin four decades ago. We're everyday people who deliver extraordinary results. Innovation, creativity, and urgency aren’t buzzwords, they’re expectations. And just like the real protein snacks we make across our global house of brands—[Jack Link’s®](https://nam02.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.jacklinks.com%2F&data=05%7C02%7Cemma.gibson%40jacklinks.com%7C78c6c2e431a841c1d33108dea7c282ae%7Cc88406accc954243baaeecf33e36426b%7C1%7C0%7C639132651014944412%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=V2oFK%2Bp7SVRKcjqPZE2tDhTz7SYv1UPeWIia5wxlD%2Bo%3D&reserved=0) , [Lorissa’s Kitchen®](https://nam02.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.lorissaskitchen.com%2F&data=05%7C02%7Cemma.gibson%40jacklinks.com%7C78c6c2e431a841c1d33108dea7c282ae%7Cc88406accc954243baaeecf33e36426b%7C1%7C0%7C639132651014977670%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=4PvtVZ5kKhb5lhrUa0zDB62ma%2B1ppalj9j1yyNxy78M%3D&reserved=0) , [Golden Island®](https://nam02.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.goldenislandjerky.com%2F&data=05%7C02%7Cemma.gibson%40jacklinks.com%7C78c6c2e431a841c1d33108dea7c282ae%7Cc88406accc954243baaeecf33e36426b%7C1%7C0%7C639132651014994227%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=Glkoavxz2X%2FRCA%2B6Q4hW%2FsMGRtFodYD6o3YphfJHc2U%3D&reserved=0) , [BiFi®](https://nam02.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.bifi.com%2Fen&data=05%7C02%7Cemma.gibson%40jacklinks.com%7C78c6c2e431a841c1d33108dea7c282ae%7Cc88406accc954243baaeecf33e36426b%7C1%7C0%7C639132651015011537%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=y98jBJUjgw8%2BY7J12IjZkCAxeHUkIjFfFCLcUAotHF0%3D&reserved=0) , and [Peperami®](https://nam02.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.peperami.tv%2F&data=05%7C02%7Cemma.gibson%40jacklinks.com%7C78c6c2e431a841c1d33108dea7c282ae%7Cc88406accc954243baaeecf33e36426b%7C1%7C0%7C639132651015027090%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=maSudYWEjlvlFvBXqcaFaX56AqyfJWZw2ROsbOEsdrg%3D&reserved=0) and [KOOEE!®](https://nam02.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.kooeesnacks.com.au%2F&data=05%7C02%7Cemma.gibson%40jacklinks.com%7C78c6c2e431a841c1d33108dea7c282ae%7Cc88406accc954243baaeecf33e36426b%7C1%7C0%7C639132651015041988%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=lD8PvmZrxa%2BvVVxh64TVK6ZeqkTiHmzQNd97ulmTiN8%3D&reserved=0) to name a few—there’s nothing artificial about us. What you see is exactly what you get: humble, gritty, passionate people who show up every day ready to not just be a participate in the meat snack industry that the Link Family created, but to move faster, innovate harder and keep raising the bar so high, the rest of the world needs a ladder just to see it. Dominating this space across the world takes a team. A team that runs together, succeeds together, and celebrates together. A team that’s full of relentless energy and spirit that can only be fueled by one thing: a fist full of our delicious meat snacks. Real Meat Protein. Real People. Real Results. THAT is Link Snacks. The FSQ Auditor supports the implementation of HACCP, SOP, SQF, and R&D and performs plant-wide auditing functions. This role completes documentation; ensures that product specifications are met; customer quality expectations are achieved; USDA regulations are complied with; all quality issues are identified, investigated, and addressed. Monitoring room temperatures, monitoring product temperatures, and monitoring product quality/consistency. Shift: 2nd Shift Monday - Thursday, 2:30pm to 1:00am Wage: $23.00 to $25.00 per hours ( $20.00 to $22.00 per hours PLUS $3.00 Shift Differential) DUTIES AND RESPONSIBILITIES The duties and responsibilities of this position shall consist of, but not be limited to, the following: * Perform quality inspections on random product samples to ensure samples meet company specific Quality standards. [For example: thickness, weights, lengths, count, metal detector, etc.] * Perform pre-op – depending on time, scheduling and production including first piece checks at start of shift or new product changeover. * Monitoring the overall safety of the food quality to ensure accurate product identification and recipe instructions are being followed. Answer questions regarding rejected product, damage on inbound cases and mislabeled cases. * Follow plant holds and releases. * Enter quality inspection data into electronic/written form. * Record deviations/issues into compliance tracker and inform lead/supervisor of said deviations or defects. * Process inbound and outbound supplier corrective action requests. * Perform weekly daily audits. * Prepares necessary forms and trend charts in support of kitchen or packaging inspection function. * Implement corrective actions on deviations found during quality inspections, including product loss or adjustments. * Review of documentation for accuracy and completeness. * HACCP sign off – dependent on qualifications and availability. * Review/Close out hold tags as necessary- list should be printed off daily, hold tags must be accounted for; report missing hold tags to lead/supervisor. * Verify equipment is in good condition and calibrated, as needed. * HACCP, SSOP, SQF, Prerequisite program maintenance - accuracy, completeness, implementation; aligned with review of production paperwork, verifications, calibrations, and counseling, etc. * Follow Good Manufacturing Practices (GMPs), Hazard Analysis and Critical Control Point (HACCP) training, along with company pre-requisite programs, Standard Operating Procedures (SOP’s), and Standard Sanitation Operating Procedures (SSOP’s). Observe team members to ensure compliance, coach as necessary. * Acts as a backup for daily operational checklists. * Assist Quality Control Supervisor with serious or repeated quality problems to help determine the cause and prevent further occurrences. * Maintain SQF and HACCP book, keep documents up to date. * Assist with Quality Control and Production audits. * Performs other duties and responsibilities as necessary. Safety * Perform all duties within OSHA and company safety standards; LOTO, wear PPE and maintain safety equipment. * Maintain a safe, clean and organized work area. * Immediately report all accidents and deficiencies to the lead/foreman/supervisor. * Ensure safety devices are installed and working properly. * Monitor work environment for general food safety hazards such as condensation monitoring, etc. Communication * Communicate with coworkers and leaders in an effective, timely manner. * Keep foreman/supervisor informed daily of problems incurred during the shift. * Suggest improvements; continuously improve the quality of all support activities. ## Qualifications REQUIRED EDUCATION AND EXPERIENCE Required Education : High school diploma or GED Required Experience : 1-2 years of experience and/or training in a manufacturing or food environment Preferred : * Knowledge and experience in quality systems and production * Prior knowledge of food processing equipment * Basic knowledge of supply chain, purchasing, materials and/or manufacturing * Knowledge of SAP * HACCP certification preferred, must be completed within 6 months * Ability to calibrate delicate instruments and take accurate readings on fine gauges. * College degree REQUIRED SKILLS, KNOWLEDGE and ABILITIES : * An aptitude for math is required. * Ability to work under pressure, meet deadlines and handle multiple projects simultaneously. * Superior accuracy and attention to detail. * Ability to find a solution for or to deal proactively with work-related problems * Ability to read and interpret documents such as safety rules, operating and/or maintenance instructions and procedure manuals. * Strong verbal and written communication skills in English. * Ability to carry out detailed but uninvolved written or oral instructions. * Ability to organize and prioritize in a multi-tasking environment * Ability to collaborate with remote employees and work as part of a team. * Must have exceptional time management skills. * Firm knowledge of quality assurance methods, product testing methods, standard measurements, regulatory compliance standards, and documentation procedures * Proficient in Internet navigation, Microsoft Word, Excel, PowerPoint, and Outlook. * Must demonstrate effective leadership, problem solving, presentation, and employee motivational skills. ## Additional Information PHYSICAL DEMANDS : The physical demands described here are representative of those that must be met by an employee to be successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job the employee is regularly required to stand, walk, use hands to finger, handle, or feel, lift and/or move up to 25 pounds, and talk or hear. The employee is occasionally required to sit, and reach with hands and arms. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision. WORK ENVIRONMENT : The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. The work environment is a plant / office setting with varying degrees of temperatures and noise levels. Exposure to manufacturing equipment movement and wet / slippery floors. Travel may be required. Equal Employment Opportunity Employer Jack Link's is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation and gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. E-Verify Jack Link's provides the Social Security Administration (SSA) and, if necessary, the Department of Homeland Security (DHS), with information from each new Team Member’s Form I-9 to confirm work authorization. IMPORTANT: If the Government cannot confirm that you are authorized to work, we are required to provide you written instructions and an opportunity to contact SSA and/or DHS before taking adverse action against you, including terminating your employment. We do not use E-Verify to pre-screen job applicants or to re-verify current employees and may not limit or influence the choice of documents presented for use on the Form I-9. In order to determine whether Form I-9 documentation is valid, we use E-Verify’s photo screening tool to match the photograph appearing on some permanent resident and employment authorization cards with the official U.S. Citizenship and Immigration Services’ (USCIS) photograph. If you believe that Jack Link’s has violated our responsibilities under this program or has discriminated against you during the verification process based upon your national origin or citizenship status, please call the Office of Special Counsel at 1-800-255-7688 (TDD: 1-800-237-2515). All your information will be kept confidential according to EEO guidelines.", "summaryDescription" : "FSQ Auditor at Jack Link's Protein Snacks", "postedDate" : "2026-06-15T21:18:57.000", "createdAt" : "2026-06-16T00:28:11.230", "lastUpdated" : "2026-06-16T09:42:22.905", "ingestTimestamp" : "2026-06-16T00:28:11.230", "mongoId" : "6a306d86f292fd229cfd8e7c", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 75000, "salaryAnnualMax" : 105000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.8888889, "_score" : 644.62897, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Food & Beverage", "llmIndustryConfidence" : 0.95 }, { "id" : "6a3051c6f292fd229cf068b7", "title" : "Senior Software Engineer - Device Experience", "company" : "Easygo", "industry" : "Technology", "salary" : { "min" : 155000.0, "max" : 215000.0, "currency" : "AUD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimation is based on the market baseline for a Senior Software Engineer in Melbourne, Australia, adjusted for the technology industry and company size." }, "location" : "Melbourne, Victoria, Australia", "locations" : [ "Melbourne", "Victoria", "Australia" ], "timestamp" : "2026-06-16T07:40:32.723", "fingerprint" : "bafb1434aeb4ede74fc04aaff191521675a27225ded20baa7a90c573e0a4dd4c", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/easygo/jobs/5164497007", "externalId" : "5164497007", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Melbourne", "state" : "Victoria", "country" : "Australia", "continent" : "oc", "source" : "llm", "workMode" : "hybrid", "geo" : "-37.8142454,144.9631732" } ], "locationText" : "Melbourne, Victoria, Australia", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 4, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "remoteFriendly" : true, "workSiteFlexibility" : "Flexible", "rawDescription" : "Engineering@Easygo At Easygo, our Core team is at the heart of our operations, creating the robust, high-performance backend software that underpins both our global casino games and sportsbook offerings. The exciting thing about the Core team is that it impacts every single customer and is felt directly by every engineer across all feature development squads within the world's largest online crypto casino and sportsbook platform. As a dedicated developer experience team, we tackle complex technical challenges with innovation and precision, ensuring the foundational systems are robust, scalable, and empower all product development teams. If you're passionate about growth, innovation, and working with the best, we'd love to have you on our team! Key Responsibilities: Deliver high-quality, well-tested features and improvements across the app estate with a strong focus on correctness, performance, and platform best practices. Contribute meaningfully to architectural and technical design discussions within your platform domain, raising considerations around scalability, stability, and maintainability. Uphold and actively contribute to engineering standards including code review rigour, testing coverage, CI/CD adherence and the team's Definition of Done. Partner with Product Managers, UX Designers, and Backend Platform Engineers to deliver user experiences that are seamless and leverage platform capabilities effectively. Identify and surface blockers, technical risks, and delivery concerns early - taking a proactive approach to problem-solving rather than waiting to be directed. Support the growth of the team by providing constructive code review feedback, sharing knowledge openly, and offering guidance to less experienced engineers. Contribute to improving crash-free rates, release predictability, and app stability - key engineering metrics for the Device Experiences team. Participate in on-call and incident response activities, taking ownership of issues within your domain through to resolution. Qualifications: Bachelor's/Master's degree in Computer Science or equivalent practical experience. 4+ years of hands-on experience in mobile software engineering with a focus on quality delivery and scalable development. Proficiency in one or more mobile platforms, with familiarity in the relevant ecosystem and frameworks. Solid understanding of mobile development lifecycles including design, testing, release pipelines, and production support. Experience working with RESTful APIs to connect mobile applications to back-end services. Good understanding of mobile platform design principles and interface guidelines. Strong communication skills with the ability to collaborate effectively across engineering, product, and design. A track record of delivering reliable, well-tested features in a team environment. Experience building and maintaining large-scale consumer mobile applications. Familiarity with CI/CD pipelines and automated testing frameworks for mobile. Experience debugging production issues and contributing to incident resolution. Demonstrated ability to lead delivery of a feature or component from design to production. Experience building custom UI components, video players, or animations. Exposure to regulated market app delivery or multi-variant build pipelines. A quick learner who embraces new technologies and adapts to changing priorities. Some of the perks of joining us: Champion Engineering Excellence to influence cultural change across the organisation. Work alongside the top 5% of engineering talent in Australia, using a vast cloud native tech stack including AWS, Microservices, Large-Scale Distributed Systems, NATS, K8's, ArgoCD, Terraform, Typescript, GraphQL, Nodejs. Exposure to building global, large-scale volume products which operate at thousands per second frequency. Be rewarded with lucrative annual bonuses Enjoy 30 days of bundled person leave - choose how you use it! Give back with a paid volunteer day Fuel your day with daily breakfast and open pantries brimming with unlimited snacks and refreshments, all on the house Break up the week with on site remedial massage Wednesdays In house full-time barista’s providing you your daily coffee needs Weekly team lunches and happy hour in the office from 4pm on Fridays Enjoy a bustling office with the option for up to 2 days work from home per week Fun office environment with pool tables, table tennis and all your favourite gaming consoles We believe that the unique contributions of everyone at Easygo are the drivers of our success. To make sure that our products and culture continue to incorporate everyone's perspectives and experiences we never discriminate on the basis of race, religion, national origin, gender identity or expression, sexual orientation, age, marital, veteran, or disability status. We are passionate about providing a workplace that encourages great participation and an equal playing field, where merit and accomplishment are the only criteria for success.", "summaryDescription" : "Senior Software Engineer - Device Experience at Easygo", "postedDate" : "2026-06-15T23:21:20.914", "createdAt" : "2026-06-15T23:21:20.914", "lastUpdated" : "2026-06-16T07:40:32.723", "ingestTimestamp" : "2026-06-15T23:21:20.914", "mongoId" : "6a3051c6f292fd229cf068b7", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "150k-200k", "hasSalary" : false, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 0.8888889, "_score" : 638.83673, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.98 }, { "id" : "68ed10aa70f0b99d58e7b9ce", "title" : "Device Associate, Quality Services, Device Tech Support", "company" : "Amazon Development Centre (India) Private Limited", "industry" : "Operations, IT, Support Engineering, Device Associates, alexa and amazon devices", "salary" : { "min" : 450000.0, "max" : 750000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on the market baseline for an entry-level Device Associate, Quality Services, Device Tech Support role in Chennai, India, with adjustments for the technology industry and company size." }, "location" : "Chennai, Tamil Nadu, IND", "locations" : [ "Chennai, Tamil Nadu, IND" ], "timestamp" : "2026-06-15T03:43:04.750", "fingerprint" : "dfb26c9745ac7ec8a0cb503817016c4709ff1f1aba84eaf10b1bf25d76f1b8c0", "source" : "amazon", "language" : "en", "applyUrl" : "https://account.amazon.com/jobs/3105289/apply", "externalId" : "9a3dc30f-928b-4f64-ad9d-66f7ae8f52b9", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Chennai", "state" : "Tamil Nadu", "country" : "India", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "13.0836939,80.2701860" } ], "locationText" : "Chennai, Tamil Nadu, India", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "coreResponsibilities" : "Execute test plans, Execute test cases, Create test data, Report results, Understand project functionality, Stay connected with requirements, Stay connected with documentation, Look for gaps in test cases, Look beyond test cases for issues, Execute processes to test product changes, Backtrack bugs, Backtrack issues, Perform root cause analysis of bugs, Perform root cause analysis of issues, Execute regression cases, Raise bugs, Support ad-hoc requests, Interact with QA for new features, Support first pass, Support bug repro, Contribute ideas, Take part in implementing ideas", "teamCollaboration" : "Interacting with QA", "domainKnowledge" : "E-reader devices", "domainList" : [ "e-reader-devices" ], "domainSpecificKnowledge" : [ "E-reader devices" ], "problemSolvingSkills" : "Root cause analysis", "qualificationsBasic" : "Bachelor's degree, Knowledge of QA methodology, Knowledge of QA tools", "qualificationsPreferred" : "Good Communication, Testing Knowledge, Good Analytical Skill", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "At this role the associate gets a chance to work on multiple generations of E-reader devices and will directly contribute to the high quality of the devices. Key job responsibilities - Execute test plans & test cases, creating test data, and reporting results in a timely, clear, and concise manner. - Should have understanding of the functionality of the project/product. Should have the ability to stay connected with changing requirements and documentation. - Should be able to actively look for gaps in test cases and look beyond test cases for issues/bugs. - Should execute processes to thoroughly test product changes. - Should have the ability to backtrack and do a root cause analysis of bugs/issues. A day in the life A typical day involves executing regression cases , raising bugs, supporting ad-hoc requests etc. Also involves interacting with QA for new features, supporting first pass and bug repro. Contributing ideas and take part in implementing them About the team Highly energetic and fun loving team with great flexibility. Team contributes to multiple aspect of the quality of E-reader devices. Handles multiple parallel releases successfully. Basic Qualifications: - Bachelor's degree - Knowledge of QA methodology and tools Preferred Qualifications: - Good Communication - Testing Knowledge - Good Analytical Skill 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" : "Device Associate, Quality Services, Device Tech Support at Amazon Development Centre (India) Private Limited. Execute test plans. Execute test cases", "postedDate" : "2026-06-13T20:37:02.797", "createdAt" : "2026-06-13T20:37:02.797", "lastUpdated" : "2026-06-15T03:43:04.750", "ingestTimestamp" : "2026-06-13T20:37:02.797", "mongoId" : "68ed10aa70f0b99d58e7b9ce", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.com/jobs/3105289/apply", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "E-reader devices" ], "skillCount" : 1, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Entry", "dataQualityScore" : 0.8888889, "_score" : 638.75415, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.95 }, { "id" : "69164d9270f0b99d586f2a43", "title" : "Quality Auditor - Portuguese", "company" : "Amazon Support Services Costa Rica SRL", "industry" : "Systems, Quality, Security Engineering, Machine Learning Data Operatio, Artificial Intelligence", "salary" : { "min" : 1.4E7, "max" : 1.9E7, "currency" : "CRC", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-seniority Quality Auditor in the Technology industry in Heredia, Costa Rica, adjusted for company size and specific role requirements." }, "location" : "Heredia, Heredia, CRI", "locations" : [ "Heredia, Heredia, CRI" ], "timestamp" : "2026-06-15T02:10:28.374", "fingerprint" : "941ca5aa50a8828b55a126e0ad2bbc23eab649aaab4290a26fa2967b46bbdf92", "source" : "amazon", "language" : "en", "applyUrl" : "https://account.amazon.com/jobs/3122333/apply", "externalId" : "05c27870-3b9e-4e75-aaae-229087b476b0", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Heredia", "state" : "Heredia", "country" : "Costa Rica", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "9.9984272,-84.1171215" } ], "locationText" : "Heredia, Heredia, Costa Rica", "employmentType" : "FULL_TIME", "technicalSkills" : "Excel, Data analysis", "professionalSkills" : [ "Quality management", "Data annotation", "Quality metrics" ], "hardSkillsList" : [ "Manual review", "Data validation", "Root cause analysis", "Quality auditing" ], "softSkillsList" : [ "Adaptability" ], "hardSkills" : [ { "name" : "Manual review", "level" : "intermediate" }, { "name" : "Data validation", "level" : "intermediate" }, { "name" : "Root cause analysis", "level" : "intermediate" }, { "name" : "Quality auditing", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Adaptability" } ], "majorSkills" : "Quality assurance, Data quality, Portuguese fluency", "majorSkillsList" : [ "Quality assurance", "Data quality", "Portuguese fluency" ], "coreResponsibilities" : "Conduct quality audits, Provide detailed insights, Identify root causes, Perform manual reviews, Validate automated quality measurements, Document quality findings, Report quality findings, Perform audits for deep dives, Perform audits for escalations, Coach Data Associates, Calibrate Data Associates, Maintain compliance with quality standards, Maintain compliance with procedures, Improve processes, Implement best practices, Contribute to continuous improvement", "teamCollaboration" : "Quality Specialists; Quality Audit Managers", "domainKnowledge" : "Data annotation; Quality metrics; AI; Machine learning", "domainList" : [ "data-annotation", "quality-metrics", "ai", "machine-learning" ], "domainSpecificKnowledge" : [ "Data annotation", "Quality metrics", "AI", "Machine learning" ], "toolProficiency" : [ "Excel", "Data analysis tools" ], "documentationSkills" : "Document findings", "problemSolvingSkills" : "Problem-solving; Root cause analysis", "qualificationsBasic" : "CEFR C1+ fluency in Portuguese, Analytical skills, Problem-solving skills, Excellent attention to detail, Experience with quality management tools, Ability to work in strict compliance, Understanding of data annotation, Understanding of quality metrics, Proficiency in Excel, Proficiency in data analysis tools, Ability to work effectively in a team", "qualificationsPreferred" : "Prior experience in QA, Experience in tech industry, Familiarity with AI concepts, Familiarity with machine learning concepts, Experience with speech data, Experience with language data", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "We are seeking a detail-oriented Quality Auditor to join our team at AGI-DS. As a Quality Auditor, you will perform systematic quality assessments within our global network of Data Associates, providing manual review and validation of automated quality measurements. This role is critical in maintaining high standards in data quality for AI development and training. Key job responsibilities Conduct quality audits on individual workflows and units delivered by Data Associates Provide detailed insights on Data Associate-level quality and identify root causes of issues Perform manual reviews to validate automated quality measurement systems Document and report quality findings accurately and efficiently Perform audits to support deep dives and escalations as needed Coach and calibrate Data Associates co-located at your site to improve performance Maintain strict compliance with quality standards and procedures Work closely with Quality Audit Managers to improve processes and implement best practices Contribute to continuous improvement initiatives within the quality assurance team A day in the life You'll be auditing data from Data Associates, ensuring the data aligns with our Quality standards and providing detailed feedback to annotators if the data does not meet our standards. You'll collaborate with Quality Specialists to affirm audit strategies, provide insights, and discuss trends. About the team We are a specialized team of Quality Auditors whose strength lies in our attention to detail and documenting feedback for relevant stakeholders. We approach each audit with singular focus and apply our findings to a broad perspective, certifying if data quality is at our standards. Our collaborative methods ensure that insights are refined and lead to comprehensive and reliable audit results. Basic Qualifications: - CEFR C1+ or equivalent fluency in Portuguese - Strong analytical and problem-solving skills - Excellent attention to detail - Experience with quality management tools and systems - Ability to work in strict compliance with internal guidelines - Understanding of data annotation and quality metrics - Proficiency in Excel and data analysis tools - Ability to work effectively in a team environment - Adaptability to changing priorities and workloads Preferred Qualifications: - Prior experience in a quality assurance role within the tech industry - Familiarity with AI and machine learning concepts - Experience with speech or language data 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 Auditor - Portuguese at Amazon Support Services Costa Rica SRL. Skills: Quality assurance, Data quality, Portuguese fluency. Conduct quality audits. Provide detailed insights", "postedDate" : "2026-06-12T23:04:18.470", "createdAt" : "2026-06-12T23:04:18.470", "lastUpdated" : "2026-06-15T02:10:28.374", "ingestTimestamp" : "2026-06-12T23:04:18.470", "mongoId" : "69164d9270f0b99d586f2a43", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.com/jobs/3122333/apply", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Manual review", "Data validation", "Root cause analysis", "Quality auditing", "Adaptability", "Quality assurance", "Data quality", "Portuguese fluency", "Quality management", "Data annotation", "Quality metrics", "AI", "Machine learning", "Excel", "Data analysis tools" ], "skillCount" : 15, "jobCategory" : "engineering", "dataQualityScore" : 0.8888889, "_score" : 637.6014, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a2c7d3274d8ee00a094f3d0", "title" : "Senior Internal Auditor", "company" : "Braze", "industry" : "SaaS", "salary" : { "min" : 145000.0, "max" : 210000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Senior Internal Auditor in New York, adjusted for SaaS industry and company size." }, "location" : "New York City", "locations" : [ "New York City" ], "certifications" : [ "CPA", "CIA", "CISA" ], "timestamp" : "2026-06-15T08:27:17.860", "fingerprint" : "846b8c0bf86f2504b2c1f0c448a9df5bcaece0cae4a8d1dc1be5be96d5fb0bbe", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://boards.greenhouse.io/braze/jobs/7993760?gh_jid=7993760", "externalId" : "7993760", "industryFunction" : { }, "structuredLocations" : [ { "city" : "New York", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.7127281,-74.0060152" } ], "locationText" : "New York, New York, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Data analysis, SQL", "professionalSkills" : [ "Risk assessment", "Internal controls", "Process improvement" ], "hardSkillsList" : [ "SOX compliance", "Operational audits", "Audit analytics", "Risk management", "Control testing", "Remediation validation", "Technology audits", "Risk assessments", "Automated controls", "System implementations", "Enterprise Risk Management", "Data analytics", "Continuous monitoring", "Automation", "AI-driven audit", "Audit execution", "Audit documentation", "Audit reporting", "Audit methodologies", "Audit standards" ], "softSkillsList" : [ "Intellectually curious", "Analytical" ], "hardSkills" : [ { "name" : "SOX compliance", "level" : "intermediate" }, { "name" : "Operational audits", "level" : "intermediate" }, { "name" : "Audit analytics", "level" : "intermediate" }, { "name" : "Risk management", "level" : "intermediate" }, { "name" : "Control testing", "level" : "intermediate" }, { "name" : "Remediation validation", "level" : "intermediate" }, { "name" : "Technology audits", "level" : "intermediate" }, { "name" : "Risk assessments", "level" : "intermediate" }, { "name" : "Automated controls", "level" : "intermediate" }, { "name" : "System implementations", "level" : "intermediate" }, { "name" : "Enterprise Risk Management", "level" : "intermediate" }, { "name" : "Data analytics", "level" : "intermediate" }, { "name" : "Continuous monitoring", "level" : "intermediate" }, { "name" : "Automation", "level" : "intermediate" }, { "name" : "AI-driven audit", "level" : "intermediate" }, { "name" : "Audit execution", "level" : "intermediate" }, { "name" : "Audit documentation", "level" : "intermediate" }, { "name" : "Audit reporting", "level" : "intermediate" }, { "name" : "Audit methodologies", "level" : "intermediate" }, { "name" : "Audit standards", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Intellectually curious" }, { "name" : "Analytical" } ], "majorSkills" : "SOX compliance, Internal controls, Risk management, Data analytics", "majorSkillsList" : [ "SOX compliance", "Internal controls", "Risk management", "Data analytics" ], "coreResponsibilities" : "Perform SOX testing activities, Coordinate with internal stakeholders, Monitor and validate remediation activities, Assist in execution of audits, Support audit planning activities, Assess business processes, Support Enterprise Risk Management activities, Leverage data analytics and audit tools, Support continuous monitoring, automation, and AI-driven audit initiatives, Leverage tools such as Jira, Workiva, and data, Support preparation in clear and concise audit reports, Facilitate meetings, Contribute to continuous improvement of Internal Audit methodologies", "teamCollaboration" : "Partner with stakeholders; Coordinate with external auditors; Coordinate with co-source providers; Communicate audit results to stakeholders", "projectManagementSkills" : [ "Agile" ], "domainKnowledge" : "SaaS environment; Subscription revenue; Professional services revenue; Financial process controls; IT General Controls", "domainList" : [ "saas-environment", "subscription-revenue", "professional-services-revenue", "financial-process-controls", "it-general-controls" ], "domainSpecificKnowledge" : [ "SaaS environment", "Subscription revenue", "Professional services revenue", "Financial process controls", "IT General Controls" ], "toolProficiency" : [ "Jira", "Workiva", "Data analytics platforms" ], "communicationSkills" : "Audit reports; Presentations; Executive communications", "documentationSkills" : "Documentation updates; Audit workpapers", "continuousLearning" : "Learning platforms; Yearly learning stipend", "problemSolvingSkills" : "Root cause analysis", "qualificationsBasic" : "B. S. in Accounting, Finance, Information Systems, 3 years minimum relevant experience, Software/SaaS or Technology industry experience, Demonstrated experience with Sarbanes-Oxley compliance, Demonstrated experience with internal controls, Demonstrated experience with risk management, Skills in data analysis, Writing SQL queries, Understanding database structures, Extracting actionable insights from complex datasets", "qualificationsPreferred" : "Professional certification such as CPA, CIA or CISA, Public Accounting or industry experience, Financial process and IT General Controls", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "At Braze, we have found our people. We’re a genuinely approachable, exceptionally kind, and intensely passionate crew. We seek to ignite that passion by setting high standards, championing teamwork, and creating work-life harmony as we collectively navigate rapid growth on a global scale while striving for greater equity and opportunity – inside and outside our organization. To flourish here, you must be prepared to set a high bar for yourself and those around you. There is always a way to contribute: Acting with autonomy, having accountability and being open to new perspectives are essential to our continued success. Our deep curiosity to learn and our eagerness to share diverse passions with others gives us balance and injects a one-of-a-kind vibrancy into our culture. If you are driven to solve exhilarating challenges and have a bias toward action in the face of change, you will be empowered to make a real impact here, with a sharp and passionate team at your back. If Braze sounds like a place where you can thrive, we can’t wait to meet you. What We’re Looking For We are seeking a Senior Internal Auditor to support and help evolve our Internal Audit function. This role is ideal for a hands-on audit professional who is eager to contribute across SOX compliance, operational audits, enterprise risk management, and audit analytics within a fast-paced, high-growth SaaS environment. Reporting to Internal Audit leadership, you will partner with stakeholders across Technology, Engineering, Finance, Legal, Security, and other business functions to evaluate risk, strengthen internal controls, and identify opportunities to improve business processes. You will play a key role in executing risk-based audit activities while helping the team leverage automation, data analytics, and continuous monitoring techniques to enhance audit effectiveness and efficiency. The ideal candidate has experience with SOX compliance, internal controls, and audit execution within a public company, public accounting, or technology-focused environment. You are intellectually curious, analytical, highly collaborative, and comfortable operating in an Agile environment. What You’ll Do Perform SOX testing activities, including walkthroughs, control testing, documentation updates, deficiency tracking, and remediation validation. Coordinate with internal stakeholders, external auditors, and co-source providers to facilitate audit execution and evidence collection. Monitor and validate remediation activities to ensure timely resolution of identified issues and control deficiencies. Assist in the execution of risk-based operational, compliance, financial, and technology audits from planning through reporting. Support audit planning activities by conducting risk assessments, gathering information, and preparing audit workpapers. Assess business processes, automated controls, and system implementations to identify control gaps and process improvement opportunities. Support quarterly Enterprise Risk Management (ERM) activities, including risk identification, risk scoring, mitigation tracking, and reporting. Leverage data analytics and audit tools to enhance testing effectiveness, identify trends, and provide actionable insights to stakeholders. Support continuous monitoring, automation, and AI-driven audit initiatives to improve audit coverage and efficiency. Leverage tools such as Jira, Workiva, and data analytics platforms to enhance audit execution, documentation, and reporting processes. Support preparation in clear and concise audit reports, presentations, and executive-ready communications that summarize risks, observations, and recommendations. Facilitate meetings, document key discussions and action items, and effectively communicate audit results to stakeholders. Contribute to the continuous improvement of Internal Audit methodologies, standards, and operational practices. Who You Are To excel in this role, you will need a combination of technical expertise, interpersonal skills, and a commitment to upholding regulatory standards. Key qualifications and attributes we're looking for include: B. S. in Accounting, Finance, Information Systems or related area Professional certification such as CPA, CIA or CISA 3 years minimum relevant experience, including Public Accounting or industry experience Software/SaaS or Technology industry experience with subscription and professional services revenue Demonstrated experience with Sarbanes-Oxley compliance, internal controls (ideally, both financial process and IT General Controls), and risk management within a corporate environment. Strong skills in data analysis, including writing SQL queries, understanding database structures, and extracting actionable insights from complex datasets. Proven track record of supporting audits, note-taking, and facilitating meetings, ideally in international settings. Strong leadership skills, high EQ and proactive problem solving approach Ability to collaborate with onshore and offshore team(s) Experience using Workiva GRC platform is a plus Experience with agile project management methodologies a plus For candidates based in the United States, the pay range for this position at the start of employment is expected to be between $83,000 and $125,000/year, with an expected On Target Earnings (OTE) between $93,000 and $140,000/year (including bonus or commission). Your exact offer may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition to cash compensation, this role qualifies for a comprehensive Total Rewards package that includes equity grants of restricted stock (RSUs) so that you will own a piece of our company. WHAT WE OFFER Braze benefits vary by location, and we encourage you to review our specific benefits offerings for each country here. More details on benefits plans will be provided if you receive an offer of employment. From offering comprehensive benefits to fostering hybrid ways of working, we’ve got you covered so you can prioritize work-life harmony. Braze offers benefits such as: Competitive compensation that may include equity Retirement and Employee Stock Purchase Plans Flexible paid time off Comprehensive benefit plans covering medical, dental, vision, life, and disability Family services that include fertility benefits and equal paid parental leave Professional development supported by formal career pathing, learning platforms, and a yearly learning stipend A curated in-office employee experience, designed to foster community, team connections, and innovation Opportunities to give back to your community, including an annual company-wide Volunteer Week and donation matching Employee Resource Groups that provide supportive communities within Braze Collaborative, transparent, and fun culture recognized as a Great Place to Work® ABOUT BRAZE Braze is the leading customer engagement platform that empowers brands to Be Absolutely Engaging™. Braze helps brands deliver great customer experiences that drive value both for consumers and for their businesses. Built on a foundation of composable intelligence, BrazeAI™ allows marketers to combine and activate AI agents, models, and features at every touchpoint throughout the Braze Customer Engagement Platform for smarter, faster, and more meaningful customer engagement. From cross-channel messaging and journey orchestration to Al-powered decisioning and optimization, Braze enables companies to turn action into interaction through autonomous, 1:1 personalized experiences. The company has been consistently recognized as a Leader in marketing technology by industry analysts, and was named a G2 “Best of Marketing and Digital Advertising Software Product” in 2026. Braze was also named a 2026 Best Places to Work by Built In, a 2025 America’s Greenest Companies by Newsweek, and a 2025 Fortune Best Workplace in Technology™ by Great Place To Work®. Braze is also proudly certified as a Great Place to Work® in the U.S., the UK, Australia, and Singapore. The company is headquartered in New York with offices in Austin, Berlin, Bucharest, Chicago, Dubai, Jakarta, London, Paris, San Francisco, São Paulo, Singapore, Seoul, Sydney and Tokyo. BRAZE IS AN EQUAL OPPORTUNITY EMPLOYER At Braze, we strive to create equitable growth and opportunities inside and outside the organization. Building meaningful connections is at the heart of everything we do, and that includes our recruiting practices. We're committed to offering all candidates a fair, accessible, and inclusive experience – regardless of age, color, disability, gender identity, marital status, maternity, national origin, pregnancy, race, religion, sex, sexual orientation, or status as a protected veteran. When applying and interviewing with Braze, we want you to feel comfortable showcasing what makes you you. We know that sometimes different circumstances can lead talented people to hesitate to apply for a role unless they meet 100% of the criteria. If this sounds familiar, we encourage you to apply, as we’d love to meet you. Please see our Candidate Privacy Policy for more information on how Braze processes your personal information during the recruitment process and, if applicable based on your location, how you can exercise any privacy rights.", "summaryDescription" : "Senior Internal Auditor at Braze. Skills: SOX compliance, Internal controls, Risk management, Data analytics. Perform SOX testing activities. Coordinate with internal stakeholders", "postedDate" : "2026-06-14T03:09:44.884", "createdAt" : "2026-06-14T03:09:44.884", "lastUpdated" : "2026-06-15T08:27:17.860", "ingestTimestamp" : "2026-06-14T03:09:44.884", "mongoId" : "6a2c7d3274d8ee00a094f3d0", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 145000, "salaryAnnualMax" : 210000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "SOX compliance", "Operational audits", "Audit analytics", "Risk management", "Control testing", "Remediation validation", "Technology audits", "Risk assessments", "Automated controls", "System implementations", "Enterprise Risk Management", "Data analytics", "Continuous monitoring", "Automation", "AI-driven audit", "Audit execution", "Audit documentation", "Audit reporting", "Audit methodologies", "Audit standards", "Intellectually curious", "Analytical", "Internal controls", "Risk assessment", "Process improvement", "Agile", "SaaS environment", "Subscription revenue", "Professional services revenue", "Financial process controls", "IT General Controls", "CPA", "CIA", "CISA", "Jira", "Workiva", "Data analytics platforms" ], "skillCount" : 37, "jobCategory" : "finance", "jobSubcategory" : "accounting", "seniorityLevel" : "Senior", "dataQualityScore" : 1.0, "_score" : 637.18384, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "SaaS", "llmIndustryConfidence" : 0.98 }, { "id" : "6a308b24f292fd229c0985bd", "title" : "Night Auditor", "company" : "Aspen Skiing Company", "industry" : "Hospitality", "salary" : { "min" : 36000.0, "max" : 45000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an Entry level Night Auditor in Aspen, United States, adjusted for the hospitality industry and part-time employment." }, "location" : "Aspen, CO, United States", "locations" : [ "Aspen", "CO", "United States" ], "timestamp" : "2026-06-16T11:30:21.987", "fingerprint" : "eb597d4f24ca58d7f57128c51e1776e0e90fad7451ea54b29b99a212f4882d40", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/AspenSkiingCompany/744000132254189-night-auditor-limelight-aspen-full-time-or-part-time", "externalId" : "744000132254189", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Aspen", "state" : "Colorado", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "39.1911128,-106.8235600" } ], "locationText" : "Aspen, Colorado, United States", "employmentType" : "PART_TIME", "experienceMinYears" : 2, "experienceMaxYears" : 5, "experienceLevel" : "mid", "remoteFriendly" : false, "rawDescription" : "Limelight Hotels by Aspen One provide authentic and contemporary connections to their communities and the adventures that surround them. Each Limelight hotel is inspired by place, united by purpose, defined by you and set in the heart of elevated and unique locations, each carefully designed with distinctive design and purposeful functionality, created to evoke a sense of place and a point of view. Current locations include those across Colorado in Aspen, Snowmass, Denver, and Boulder (opened August 2025); Ketchum, Idaho; Mammoth, California (opened December 2025); and Charleston, South Carolina (coming in 2028). For more information, visit [www.limelighthotels.com](https://www.limelighthotels.com/) or follow @limelighthotel on X, Instagram or Facebook. Please note that all official communications from the Talent Acquisition or Human Resources team are sent from email addresses within the notifications@smartrecruiters.com, aspen.com, aspensnowmass.com, aspenhospitality.co, limelighthotels.com & thelittlenell.com domains. Position Summary The Night Auditor balances daily financial transactions, verifies guest accounts, and ensures accurate reporting for hotel operations. This role combines overnight front desk responsibilities with accounting duties, providing guest assistance while reconciling revenue, processing payments, and preparing financial reports for management. This position reports to the Front Office Manager. This position, if full time, will cover both Limelight Aspen and Snowmass locations, 2 to 3 days per week. If part time, the position will cover Limelight Aspen solely, 2 to 3 days per week. Job Posting Deadline Applications for this position will be accepted until June 21, 2026. Essential Job Functions • Act as Front Desk Receptionist, Concierge and PBX Operator during this shift • Assist with guest requests and any guest concerns or issues • Run night audit daily processing • Notate and follow up on wakeup calls from the wakeup call sheet • Roll all expected arrivals and no shows to next day • Post overnight parking charges • Perform check in and check out duties • Compile and distribute house reports, including arrivals, departure and in-house report • Sort and file daily receipts for all restaurant outlets • Make management aware of guest’s comments and complaints • Answer incoming internal and external phone calls, as well as additional PBX (phone operator) duties as needed • Other duties as assigned ## Qualifications Education and Experience Requirements • Must be at least 18 years of age • High School Diploma or high school equivalent required • 1 year of customer/ guest experience preferred Knowledge, Skills & Abilities • Basic industry terminology • Familiar with hotel fire and safety procedures, assisting in emergency and security procedures as directed by management • Knowledge of company policies and procedures • Strong problem-solving and critical-thinking skills to address guest inquiries and resolve concerns promptly • Strong attention to detail • Active listening and interpersonal skills to personalize the guest experience • Ability to act professional in a fast-paced environment • Ability to understand written and verbal English • Ability to work independently with minimal supervision • Ability to work effectively in team settings, contributing positively to group dynamics • Ability to demonstrate expertise in the technical aspect of the job • Comply with all policies and procedures for the Front Desk department • Complete tasks and projects delegated by your manager and assist other departments as business volumes and staff levels demand ## Additional Information Work Environment & Physical Demands • Ability to stand, walk or be on your feet for extended periods of time, kneeling and bending may be required • Regularly work indoors with no adverse conditions • Must be able to occasionally lift, push or pull up to 50 lbs. individually or with assistance (weight limits can vary according to position, but no more than 50) Job Benefits This position is classified as a regular full-time position eligible for the following benefits: Enrollment dates differ across the various programs. • Health, Dental and Vision Insurance Programs • Flexible Spending Account Programs • Life Insurance Programs • Paid Time Off Programs • Paid Leave Programs • 401(k) Savings Plan • Employee Ski Pass and Dependent Ski Passes • Other company perks OR This position is classified as a regular part-time position eligible for the following benefits: Enrollment dates differ across the various programs. • Paid Time Off Programs • Paid Leave Programs • Employee Ski Pass • Other company perks The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. By accepting a position with Aspen One, Aspen Snowmass, Aspen Ventures or Aspen Hospitality you acknowledge that you are able to perform the essential functions of the job with or without reasonable accommodation. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the job. To request accommodation during the application and interviewing process, please contact Human Resources at 970-300-7700. This job description is designed to indicate the general nature and level of work. It is not designed to contain or be interpreted as a comprehensive list of all duties, responsibilities, and qualifications required of employees assigned to this job. Duties and responsibilities may change at any time with or without notice. Aspen One is an equal opportunity employer (Minority/Female/Disabled/Veteran). At Aspen One, inclusion, equity, and diversity are fundamental to fulfilling our vision of building a better workplace and better world. From our hiring practices through the entire employee experience, we embrace and celebrate the unique experiences, perspectives and cultural backgrounds that each employee brings to the workplace. We encourage diverse points of view which allows us to develop innovative solutions to the ever-evolving world of work. Aspen One strives to foster an environment where our employees feel respected, valued and empowered, and our team members are at the forefront of helping us promote and sustain an inclusive workplace that works for all. For an overview of Aspen One Company's benefits and other compensation visit [www.aspensnowmass.com/employment/benefits-and-perks](http://www.aspensnowmass.com/employment/benefits-and-perks) Aspen One participates in E-Verify. [E-Verify & Right to Work Poster](https://rise.articulate.com/share/Czdyt_D1H8detTw7YTgvC06MJRN6tLix)", "summaryDescription" : "Night Auditor at Aspen Skiing Company", "postedDate" : "2026-06-15T17:43:22.000", "createdAt" : "2026-06-16T01:42:40.602", "lastUpdated" : "2026-06-16T11:30:21.987", "ingestTimestamp" : "2026-06-16T01:42:40.602", "mongoId" : "6a308b24f292fd229c0985bd", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 36000, "salaryAnnualMax" : 45000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 0.8888889, "_score" : 636.10345, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Hospitality", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2d58da74d8ee00a0b875d2", "title" : "Director of Engineering (Medical Device)", "company" : "Neuroelectrics", "industry" : "Healthcare", "salary" : { "min" : 115000.0, "max" : 175000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Director of Engineering in Barcelona, Spain, adjusted for the healthcare industry and company size." }, "location" : "Barcelona, ES", "locations" : [ "Barcelona", "ES" ], "timestamp" : "2026-06-15T05:09:30.227", "fingerprint" : "87a1e8f8a3c942e85e9212e07df06d4b7d5bd0e3511fdd6ab811d31423dfcdb8", "source" : "personio", "language" : "en", "applyUrl" : "https://neuroelectrics.jobs.personio.de/job/2660937", "externalId" : "2660937", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Barcelona", "country" : "Spain", "continent" : "eu", "source" : "llm", "workMode" : "hybrid", "geo" : "41.3825802,2.1770730" } ], "locationText" : "Barcelona, Spain", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "technicalSkills" : "Systems engineering, Hardware engineering, Firmware engineering, Software engineering, Signal integrity, Cloud uptime, Wireless, EMC/ESD, DFM/DFT, Production test, Device control applications, Observability, Telemetry, Secure update strategy, Cybersecurity", "professionalSkills" : [ "System-level architecture", "Technical decisions", "Engineering quality", "Engineering execution", "Technical risk", "Capacity planning", "Schedule commitment", "Hiring managers", "Retaining talent", "Developing leaders", "Engineering operating system", "Configuration management", "Release discipline", "Platform modernization", "Technical debt", "Modularization", "Staged redesigns", "Design controls", "Risk management", "Traceability", "Audit-ready", "Low-noise front-ends", "Stimulation current sources", "Safety monitoring", "Software architecture", "Code review", "Product reliability", "Complaint trending", "Corrective actions", "Reliability programs", "CAPA support", "Product strategy", "Business strategy", "Technical reality", "Scope prioritization" ], "hardSkillsList" : [ "Signal quality", "Stimulation delivery", "Connectivity", "Data integrity", "Firmware reliability", "Biopotential front-ends", "Electrode interfaces", "Artifact mitigation", "Noise mitigation", "Current source design", "Compliance voltage", "Isolation", "Stimulation protocols", "Fleet management", "Remote updates", "Incident response", "Technical files", "Audit interactions" ], "softSkillsList" : [ "Leadership", "Mentoring" ], "hardSkills" : [ { "name" : "Signal quality", "level" : "intermediate" }, { "name" : "Stimulation delivery", "level" : "intermediate" }, { "name" : "Connectivity", "level" : "intermediate" }, { "name" : "Data integrity", "level" : "intermediate" }, { "name" : "Firmware reliability", "level" : "intermediate" }, { "name" : "Biopotential front-ends", "level" : "intermediate" }, { "name" : "Electrode interfaces", "level" : "intermediate" }, { "name" : "Artifact mitigation", "level" : "intermediate" }, { "name" : "Noise mitigation", "level" : "intermediate" }, { "name" : "Current source design", "level" : "intermediate" }, { "name" : "Compliance voltage", "level" : "intermediate" }, { "name" : "Isolation", "level" : "intermediate" }, { "name" : "Stimulation protocols", "level" : "intermediate" }, { "name" : "Fleet management", "level" : "intermediate" }, { "name" : "Remote updates", "level" : "intermediate" }, { "name" : "Incident response", "level" : "intermediate" }, { "name" : "Technical files", "level" : "intermediate" }, { "name" : "Audit interactions", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "Engineering management, System architecture, Medical device development", "majorSkillsList" : [ "Engineering management", "System architecture", "Medical device development" ], "coreResponsibilities" : "Own full engineering function, Own system-level architecture, Own engineering execution end-to-end, Commit to feasibility, Build engineering team, Hire managers, Retain managers, Hire senior ICs, Retain senior ICs, Develop technical leaders, Shape engineering organization, Set engineering operating system, Plan engineering work, Review engineering work, Ship engineering work, Conduct design reviews, Conduct code reviews, Manage configuration, Automate testing, Discipline releases, Be senior technical reference, Engage on critical issues, Own product reliability, Triage issues, Trend complaints, Implement corrective actions, Manage reliability programs, Support CAPA, Drive platform modernization, Pay down technical debt, Modularize systems, Plan staged redesigns, Embed design controls, Embed risk management, Partner with RA/QA, Keep traceability audit-ready, Set direction on hardware, Set direction on firmware, Challenge hardware designs, Set direction on software, Set direction on cloud, Review software architectures, Review software code, Work as peer with Product, Work as peer with RA/QA, Work as peer with Production, Work as peer with Clinical, Work as peer with Customer Support, Bring engineering reality, Turn decisions into plans, Execute technical plans", "teamCollaboration" : "Peer with Product; Peer with RA/QA; Peer with Production; Peer with Clinical; Peer with Customer Support", "projectManagementSkills" : [ "Roadmap planning", "Scope prioritization" ], "domainKnowledge" : "Medical device software lifecycle; Usability engineering; Home healthcare environment; Connected health devices; EEG acquisition systems; Biopotential front-ends; tDCS/tACS/tRNS stimulators; Cloud-connected medical devices; EU MDR; FDA submissions", "domainList" : [ "medical-device-software-lifecycle", "usability-engineering", "home-healthcare-environment", "connected-health-devices", "eeg-acquisition-systems", "biopotential-front-ends", "tdcs-tacs-trns-stimulators", "cloud-connected-medical-devices", "eu-mdr", "fda-submissions" ], "domainSpecificKnowledge" : [ "Medical device software lifecycle", "Usability engineering", "Home healthcare environment", "Connected health devices", "EEG acquisition systems", "Biopotential front-ends", "tDCS/tACS/tRNS stimulators", "Cloud-connected medical devices", "EU MDR", "FDA submissions" ], "toolProficiency" : [ "Git", "JIRA" ], "communicationSkills" : "Technical documentation; Presentations", "documentationSkills" : "Technical documentation; Architecture diagrams; Regulatory filings; Clinical documentation", "continuousLearning" : "Professional development", "problemSolvingSkills" : "Root-cause analysis; Troubleshooting", "qualificationsBasic" : "BSc/MSc in Electrical/Electronics Engineering, Computer Engineering/Computer Science, Telecommunications, Physics, or equivalent experience, 15+ years product and system engineering experience, Several years director or head-of-engineering level experience, Demonstrated track record building and growing engineering organizations, Principal-engineer-level technical depth, Medical device experience in regulated environments, Experience with design controls, Experience with risk management, Experience with V&V, Experience with tight collaboration", "qualificationsPreferred" : "Familiarity with IEC 62304, Familiarity with IEC 62366-1, Familiarity with IEC 60601-1-11, Familiarity with Cybersecurity for connected health devices, MSc/PhD in Biomedical Engineering, Neuroengineering or related field", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Who we are Neuroelectrics is a creative, high-tech company offering the best-in-class non-invasive and high-definition electrical brain stimulation technology for personalized neuromodulation. By measuring and modifying brain function, we aim to restore brain health, minimize disabilities and create a better life for patients. We are looking for new members of our team who already live by our shared values and are inspired by our company’s Vision — accelerate the evolution of brain science and technology by delivering advanced solutions to help end patients suffering from brain pathologies — and our Mission — revolutionize the understanding of the brain through new personalized neuromodulation therapies, anywhere and at any time. Position Summary We are looking for a Director of Engineering to own the full engineering function at Neuroelectrics — systems, hardware, firmware, software — and report to the Executive Committee as the senior technical voice in the company. Product decides what we build and for whom; you own how we build it: the architecture, the technical decisions, the engineering quality, and the team that ships it. You combine principal-engineer-level technical depth with proven leadership at scale. You are hands-on by default — when a major signal-integrity issue, a stubborn architectural question, or a release-blocking bug shows up, you do not watch from the sidelines. Systems, hardware and software engineering report to you. What will you do Contribute to company-level strategy and decisions — from an engineering point of view — and put technical reality on the table when business calls are being made. Own the full engineering organization — systems, hardware, firmware, software — and the system-level architecture that ties them together. Defend it when reality pushes back. Own engineering execution end-to-end: architecture, technical design, build quality, V&V, release. Commit to feasibility, technical risk, capacity and schedule with eyes open, so Product can make scope and prioritization calls on solid ground. Build the engineering team. Hire and retain strong managers and senior Individual Contributors, develop the next layer of technical leaders, and shape an organization that matches where the product is going — not where it has been. Set the engineering operating system: how we plan, how we review, how we ship. Design and code reviews, configuration management, test automation, release discipline. Be the senior technical reference on the hardest problems: signal quality, stimulation delivery, connectivity, data integrity, firmware reliability, cloud uptime. You do not debug every issue — but when the team is stuck on something critical, you roll up your sleeves and engage at the same level as your strongest senior engineer. Own product reliability with Production and Customer Support: triage, complaint trending, corrective actions, reliability programs, and CAPA support when needed. Drive platform modernization: pay down technical debt, modularize, and plan staged redesigns that lower risk while preserving compliance. Embed design controls and risk management into how engineering really works day to day; partner with RA/QA to keep traceability audit-ready, not theatrical. Set direction on hardware and firmware: low-noise front-ends, stimulation current sources and safety monitoring, wireless, EMC/ESD, DFM/DFT, production test. You don’t design the next board yourself, but you can challenge the people who do — in detail. Set direction on software and cloud: device control applications, observability and telemetry, secure update strategy, cybersecurity for connected devices. You can review architectures and code with substance, not just slides. Work as a peer with Product, RA/QA, Production, Clinical and Customer Support. Bring engineering reality into product and business decisions; once a decision is made, turn it into a rigorous technical plan your team can execute. What do you need BSc/MSc in Electrical/Electronics Engineering, Computer Engineering/Computer Science, Telecommunications, Physics, or a similarly rigorous quantitative field (or equivalent experience). Significant experience (typically 15+ years) across product and system engineering, including several years at director or head-of-engineering level with managers as direct reports. Demonstrated track record building and growing engineering organizations: hiring strong people, developing managers, retaining technical talent, and shaping a culture where engineers do their best work. Technical depth at principal-engineer level, applied at director scope — you own system-level decisions across disciplines and have shipped products that customers depend on. Medical device experience in regulated environments: design controls, risk management, V&V, and tight collaboration with RA/QA. Familiar with ISO 13485, ISO 14971 and IEC 60601. Deep electronics background is non-negotiable: analog and mixed-signal design, embedded systems and firmware, wireless, and EMC/ESD considerations. You can read schematics, engage seriously with PCB layout and BOM choices, and challenge designs at the level your hardware leads expect — or above. Solid software engineering fundamentals — able to review architectures and major design decisions, not just project plans. Comfortable with automated testing and CI/CD as part of how engineering operates. Structured root-cause and reliability mindset: you build the systems and the team habits that close the loop from field issues to robust fixes. You will be the perfect fit if you are/have Familiarity expected (or willingness to ramp quickly) IEC 62304 (medical device software lifecycle) and IEC 62366-1 (usability engineering). IEC 60601-1-11 (home healthcare environment) for home-use contexts. Cybersecurity for connected health devices and software (e.g., IEC 81001-5-1 principles). Bonus points Background with EEG acquisition systems: biopotential front-ends, electrode interfaces, artifact and noise mitigation. (We work at microvolt scale. You know what that means.) Background with tDCS/tACS/tRNS stimulators: current source design, compliance voltage, safety monitoring, isolation, stimulation protocols. Experience leading engineering on cloud-connected medical devices: telemetry, fleet management, remote updates, incident response. Experience supporting EU MDR and/or FDA submissions — technical files, V&V, audit interactions. MSc/PhD in Biomedical Engineering, Neuroengineering or a related field. If you join us, you will enjoy: Benefits Competitive salary in the sector (according to your experience/skills). 26 vacation days per year + 24th and 31th of December. Fully stocked kitchen (Coffee, organic fruits, snacks, and beverages). Flexible Working Hours. Up to 6 days of working from home per month. Private Health insurance, including dental coverage. Professional development and collaborative environment. Unique opportunity to join our company early with excellent market traction and huge potential to grow Incredible office in Barcelona in Av. Tibidabo. (shower, stunning views of all of Barcelona, etc.) Team Building Events.", "summaryDescription" : "Director of Engineering (Medical Device) at Neuroelectrics. Skills: Engineering management, System architecture, Medical device development. Own full engineering function. Own system-level architecture", "createdAt" : "2026-06-13T23:20:04.391", "lastUpdated" : "2026-06-15T05:09:30.227", "ingestTimestamp" : "2026-06-13T23:20:04.391", "mongoId" : "6a2d58da74d8ee00a0b875d2", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "Signal quality", "Stimulation delivery", "Connectivity", "Data integrity", "Firmware reliability", "Biopotential front-ends", "Electrode interfaces", "Artifact mitigation", "Noise mitigation", "Current source design", "Compliance voltage", "Isolation", "Stimulation protocols", "Fleet management", "Remote updates", "Incident response", "Technical files", "Audit interactions", "Leadership", "Mentoring", "Engineering management", "System architecture", "Medical device development", "System-level architecture", "Technical decisions", "Engineering quality", "Engineering execution", "Technical risk", "Capacity planning", "Schedule commitment", "Hiring managers", "Retaining talent", "Developing leaders", "Engineering operating system", "Configuration management", "Release discipline", "Platform modernization", "Technical debt", "Modularization", "Staged redesigns", "Design controls", "Risk management", "Traceability", "Audit-ready", "Low-noise front-ends", "Stimulation current sources", "Safety monitoring", "Software architecture", "Code review", "Product reliability", "Complaint trending", "Corrective actions", "Reliability programs", "CAPA support", "Product strategy", "Business strategy", "Technical reality", "Scope prioritization", "Roadmap planning", "Medical device software lifecycle", "Usability engineering", "Home healthcare environment", "Connected health devices", "EEG acquisition systems", "tDCS/tACS/tRNS stimulators", "Cloud-connected medical devices", "EU MDR", "FDA submissions", "Git", "JIRA" ], "skillCount" : 70, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 635.75854, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.97 }, { "id" : "68ed10aa70f0b99d58e7b9ee", "title" : "Device Associate, Quality Services, Device Tech Support", "company" : "Amazon Development Centre (India) Private Limited", "industry" : "Operations, IT, Support Engineering, Device Associates, alexa and amazon devices", "salary" : { "min" : 450000.0, "max" : 750000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on the market baseline for an entry-level Device Associate, Quality Services, Device Tech Support role in Chennai, India, with adjustments for the technology industry and company size." }, "location" : "Chennai, Tamil Nadu, IND", "locations" : [ "Chennai, Tamil Nadu, IND" ], "timestamp" : "2026-06-15T06:10:30.037", "fingerprint" : "1e76ffaffb1bca4a2b44997d2726c1ded0f46b80e58a72aa8b075d341614e572", "source" : "amazon", "language" : "en", "applyUrl" : "https://account.amazon.com/jobs/3105252/apply", "externalId" : "d39569e1-a5cc-4e7a-bd31-71c8bb971018", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Chennai", "state" : "Tamil Nadu", "country" : "India", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "13.0836939,80.2701860" } ], "locationText" : "Chennai, Tamil Nadu, India", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "coreResponsibilities" : "Execute test plans, Create test data, Report results, Understand product functionality, Stay connected with changing requirements, Stay connected with documentation, Look for gaps in test cases, Look beyond test cases for issues, Execute processes to test product changes, Backtrack issues, Perform root cause analysis of bugs, Support ad-hoc requests, Interact with QA for new features, Support first pass, Contribute ideas, Implement ideas", "teamCollaboration" : "Interacting with QA", "domainKnowledge" : "E-reader devices", "domainList" : [ "e-reader-devices" ], "domainSpecificKnowledge" : [ "E-reader devices" ], "innovationCreativity" : "Contributing ideas; Implementing ideas", "problemSolvingSkills" : "Root cause analysis", "qualificationsBasic" : "Bachelor's degree, Knowledge of QA methodology, Knowledge of QA tools", "qualificationsPreferred" : "B. E, B. Tech. , MSC IT and MCA, Good Communication, Testing Knowledge, Good Analytical Skill", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "At this role the associate gets a chance to work on multiple generations of E-reader devices and will directly contribute to the high quality of the devices. Key job responsibilities - Execute test plans & test cases, creating test data, and reporting results in a timely, clear, and concise manner. - Should have understanding of the functionality of the project/product. Should have the ability to stay connected with changing requirements and documentation. - Should be able to actively look for gaps in test cases and look beyond test cases for issues/bugs. - Should execute processes to thoroughly test product changes. - Should have the ability to backtrack and do a root cause analysis of bugs/issues. A day in the life A typical day involves executing regression cases , raising bugs, supporting ad-hoc requests etc. Also involves interacting with QA for new features, supporting first pass and bug repro. Contributing ideas and take part in implementing them About the team Highly energetic and fun loving team with great flexibility. Team contributes to multiple aspect of the quality of E-reader devices. Handles multiple parallel releases successfully. Basic Qualifications: - Bachelor's degree - Knowledge of QA methodology and tools Preferred Qualifications: - B.E ,B.Tech. ,MSC IT and MCA - Good Communication - Testing Knowledge - Good Analytical Skill 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" : "Device Associate, Quality Services, Device Tech Support at Amazon Development Centre (India) Private Limited. Execute test plans. Create test data", "postedDate" : "2026-06-13T16:59:52.824", "createdAt" : "2026-06-13T16:59:52.824", "lastUpdated" : "2026-06-15T06:10:30.037", "ingestTimestamp" : "2026-06-13T16:59:52.824", "mongoId" : "68ed10aa70f0b99d58e7b9ee", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.com/jobs/3105252/apply", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "E-reader devices" ], "skillCount" : 1, "jobCategory" : "operations", "dataQualityScore" : 0.8888889, "_score" : 625.6622, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true }, { "id" : "69fb9bde4c40e2acd19a356f", "title" : "Senior Internal Auditor", "company" : "SMU", "industry" : "Education", "salary" : { "min" : 95000.0, "max" : 135000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Senior Internal Auditor in Dallas, TX, adjusted for the education industry and full-time employment." }, "location" : "TX-Dallas", "locations" : [ "TX-Dallas" ], "certifications" : [ "CIA", "CPA" ], "timestamp" : "2026-06-15T09:07:36.974", "fingerprint" : "1689dc6ff5db8a70ad3101157ac85d06d81bc78a92e30340b0ac3be59d03e0bf", "source" : "taleo", "language" : "en", "applyUrl" : "https://smu.taleo.net/careersection/ex/jobdetail.ftl?job=76852", "externalId" : "76852", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Dallas", "state" : "Texas", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "32.7762719,-96.7968559" } ], "locationText" : "Dallas, Texas, United States", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Microsoft Office, Data analytic tools", "professionalSkills" : [ "Risk assessment", "Internal controls", "Process improvements", "System implementations", "Project management", "Analytical skills", "Problem solving", "Interpersonal skills" ], "hardSkillsList" : [ "GAAP", "GAAS", "IIA standards" ], "softSkillsList" : [ "Professional judgment", "Professional skepticism" ], "hardSkills" : [ { "name" : "GAAP", "level" : "intermediate" }, { "name" : "GAAS", "level" : "intermediate" }, { "name" : "IIA standards", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Professional judgment" }, { "name" : "Professional skepticism" } ], "majorSkills" : "Internal audit, Risk assessment, Internal controls", "majorSkillsList" : [ "Internal audit", "Risk assessment", "Internal controls" ], "coreResponsibilities" : "Lead integrated audits, Perform integrated audits, Conduct risk assessments, Design audit objectives, Design audit scope, Evaluate internal controls, Provide advisory services, Provide consulting services, Support institutional risk awareness, Develop audit workpapers, Develop audit findings, Develop audit reports, Communicate audit results, Track management action plans, Assess management action plans, Monitor emerging risks, Monitor regulatory requirements, Monitor best practices, Contribute to improvement, Assist investigations, Assist special reviews, Assist hotline matters", "teamCollaboration" : "Partners with stakeholders; Communicate to management; Communicate to senior leadership", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Higher education; Internal auditing; Risk management; Governance processes; Financial auditing; Operational auditing; Compliance auditing; IT auditing; Strategic risk", "domainList" : [ "higher-education", "internal-auditing", "risk-management", "governance-processes", "financial-auditing", "operational-auditing", "compliance-auditing", "it-auditing", "strategic-risk" ], "domainSpecificKnowledge" : [ "Higher education", "Internal auditing", "Risk management", "Governance processes", "Financial auditing", "Operational auditing", "Compliance auditing", "IT auditing", "Strategic risk" ], "toolProficiency" : [ "Microsoft Word", "Microsoft Excel", "Microsoft PowerPoint", "Microsoft Visio" ], "communicationSkills" : "Clear communication; Effective communication; Well-structured reports", "documentationSkills" : "Audit workpapers; Audit findings; Audit reports", "continuousLearning" : "Professional development opportunities", "problemSolvingSkills" : "Root cause analysis; Problem solving", "specialRequirements" : "Sit for long periods, Walk for long distances, Handle Objects (dexterity)", "outcomesObjectives" : "Add value; Strengthen internal controls; Enhance risk management; Enhance governance processes", "qualificationsBasic" : "3 years of work experience in auditing, Bachelor's degree, Project management skills, Analytical skills, Problem solving skills, Interpersonal skills, Writing skills, Communication skills, Knowledge of GAAP, Knowledge of GAAS, Knowledge of IIA standards, Proficiency in Microsoft packages, Proficiency in data analytic tools", "qualificationsPreferred" : "Degree in Accounting, Degree in Finance, Degree in Business Administration, Degree in Operations Management, Experience with Big 4, Experience with Tier 2 public accounting firms, Experience with Higher Education Audit department, CIA, CPA, Equivalent certification", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Salary Range: Salary commensurate with experience and qualifications About SMU SMU’s more than 12,000 diverse, high-achieving students come from all 50 states and over 80 countries to take advantage of the University’s small classes, meaningful research opportunities, leadership development, community service, international study and innovative programs. SMU serves approximately 7,000 undergraduates and 5,000 graduate students through eight degree-granting schools: Dedman College of Humanities and Sciences , Cox School of Business , Lyle School of Engineering , Meadows School of the Arts , Simmons School of Education and Human Development , Dedman School of Law , Perkins School of Theology and Moody School of Graduate and Advanced Studies . SMU is data driven, and its powerful supercomputing ecosystem – paired with entrepreneurial drive – creates an unrivaled environment for the University to deliver research excellence. Now in its second century of achievement, SMU is recognized for the ways it supports students, faculty and alumni as they become ethical, enterprising leaders in their professions and communities. SMU’s relationship with Dallas – the dynamic center of one of the nation’s fastest-growing regions – offers unique learning, research, social and career opportunities that provide a launch pad for global impact. SMU is nonsectarian in its teaching and committed to academic freedom and open inquiry. About the Position: The Senior Internal Auditor provides independent and objective assurance and advisory services and independently plans and executes complex audit engagements across academic, administrative, financial, operational, compliance, IT, and strategic risk areas of the University. This role is designed to add value, strengthen internal controls, and enhance risk management and governance processes in alignment with the University’s mission and strategic plan, and the International Standards for the Professional Practice of Internal Auditing (IIA Standards). The Senior Internal Auditor exercises sound professional judgment, partners constructively with campus stakeholders, and communicates results clearly and effectively to management and senior leadership. Essential Functions: Audit Planning and Execution: - Lead and perform integrated audits (financial, operational, compliance, IT) across broad university functions. - Conduct risk assessments to identify key risk areas and contribute to the development of the annual audit plan. - Design audit objectives, scope, and procedures; evaluate internal controls for adequacy, design, and operating effectiveness. Advisory and Risk Awareness: - Provide advisory and consulting services related to internal controls, process improvements, system implementations, and emerging risks (e.g., technology, data privacy, AI governance, regulatory changes). - Support institutional risk awareness by aligning audit activities with key University risks and providing independent insight. Reporting and Communication: - Develop clear, well‑structured audit workpapers, findings, and reports that include root cause analysis, risk implications, and practical recommendations. - Communicate audit results effectively across varying levels of University management. Follow-Up and Continuous Improvement: - Track and assess management action plans to ensure timely and effective remediation of audit findings. - Monitor emerging risks, regulatory requirements, and best practices relevant to higher education. - Contribute to continuous improvement of internal audit methodologies, tools, and templates. Investigations and Special Reviews: - Assist with administrative investigations, special reviews, or hotline matters, as assigned by the Director of Internal Audit, requiring fact‑finding, analysis, and professional judgment. - Support communication of investigation results to appropriate University leadership, as directed, while maintaining sensitivity and discretion. Education and Experience: A bachelor’s degree and a minimum of three (3) years of work experience in auditing is required for this position. A degree in Accounting, Finance, Business Administration and/or Operations Management is preferred. Prior experience with “Big 4” or “Tier 2” public accounting firms or a Higher Education Audit department is desired. Knowledge, Skills and Abilities: Candidate with project management skills and ability to achieve audit objectives on multiple, complex projects running simultaneously is required. Candidate must also possess strong analytical, problem solving, and interpersonal skills. Excellent writing and communication skills is also necessary for this role. Candidate must have knowledge of Generally Accepted Accounting Principles (GAAP), Generally Accepted Auditing Standards (GAAS), and Institute of Internal Auditing (IIA) professional standards. Candidate must demonstrate proficiency in all Microsoft packages (Word, Excel, PowerPoint, Visio, etc.) and data analytic tools. Candidate with CIA and/or CPA or equivalent is preferred. Physical and Environmental Demands: Sit for long periods of time Walk for long distances Handle Objects (dexterity) Deadline to Apply: Priority consideration will be given to applications submitted by May 20, 2026. Position will remain open until filled. EEO Statement: SMU will not discriminate in any program or activity on the basis of race, color, religion, national origin, sex, age, disability, genetic information, veteran status, sexual orientation, or gender identity and expression. The Executive Director for Access and Equity/Title IX Coordinator is designated to handle inquiries regarding nondiscrimination policies and may be reached at the Perkins Administration Building, Room 204, 6425 Boaz Lane, Dallas, TX 75205, 214-768-3601, accessequity@smu.edu . Benefits: SMU offers staff a broad, competitive array of health and related benefit s. In addition to traditional benefits such as health, dental, and vision plans, SMU offers a wide range of wellness programs to help attract, support, and retain our employees whose work continues to make SMU an outstanding education and research institution. SMU is committed to providing an array of retirement programs that benefit and protect you and your family throughout your working years at SMU and, if you meet SMU's retirement eligibility criteria, during your retirement years after you leave SMU. The value of learning at SMU isn't just about preparing our students for the future. Employees have access to a wide variety of professional and personal development opportunities , including tuition benefits . USA-TX-Dallas", "summaryDescription" : "Senior Internal Auditor at SMU. Skills: Internal audit, Risk assessment, Internal controls. Lead integrated audits. Perform integrated audits", "createdAt" : "2026-06-14T06:11:29.698", "lastUpdated" : "2026-06-15T09:07:36.974", "ingestTimestamp" : "2026-06-14T06:11:29.698", "mongoId" : "69fb9bde4c40e2acd19a356f", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 95000, "salaryAnnualMax" : 135000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "GAAP", "GAAS", "IIA standards", "Professional judgment", "Professional skepticism", "Internal audit", "Risk assessment", "Internal controls", "Process improvements", "System implementations", "Project management", "Analytical skills", "Problem solving", "Interpersonal skills", "Higher education", "Internal auditing", "Risk management", "Governance processes", "Financial auditing", "Operational auditing", "Compliance auditing", "IT auditing", "Strategic risk", "CIA", "CPA", "Microsoft Word", "Microsoft Excel", "Microsoft PowerPoint", "Microsoft Visio" ], "skillCount" : 29, "jobCategory" : "finance", "jobSubcategory" : "accounting", "seniorityLevel" : "Senior", "dataQualityScore" : 0.7777778, "_score" : 625.55206, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Education", "llmIndustryConfidence" : 0.98 }, { "id" : "69ec72e84c40e2acd1d0b696", "title" : "Auditor", "company" : "Texas Workforce Commission", "industry" : "Government", "salary" : { "min" : 48000.0, "max" : 62000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline data for an entry-level Auditor in Austin, Texas, adjusted for government industry and full-time employment." }, "location" : "826917", "locations" : [ "826917", "
Austin:101 E 15th St (320-4001) (320TX-4001)
101 E 15th St
Austin, 78778-0001

" ], "certifications" : [ "Certified Public Accountant (CPA)", "Certified Internal Auditor (CIA)", "Certified Information Systems Auditor (CISA)", "Certified Texas Contract Manager" ], "timestamp" : "2026-06-16T02:38:39.455", "fingerprint" : "5147c3c4a9845c2b7a15e95ccd25ace0ea8bd4a11b5ebb58196a99451aca906a", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa270.taleo.net/careersection/ex/jobdetail.ftl?job=34602", "externalId" : "34602", "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", "minimumEducation" : "Bachelor's", "experienceMinYears" : 0, "experienceMaxYears" : 2, "experienceLevel" : "Entry", "professionalSkills" : [ "Contract monitoring", "Compliance monitoring", "Quality control", "Project management", "Process improvement", "Internal controls" ], "hardSkillsList" : [ "Auditing", "Financial performance", "IT auditing", "Business process analysis", "Agency budgetary controls", "Administrative procedures", "State regulatory laws", "Federal regulatory laws", "Audit reports", "Audit information", "Document evaluation" ], "hardSkills" : [ { "name" : "Auditing", "level" : "intermediate" }, { "name" : "Financial performance", "level" : "intermediate" }, { "name" : "IT auditing", "level" : "intermediate" }, { "name" : "Business process analysis", "level" : "intermediate" }, { "name" : "Agency budgetary controls", "level" : "intermediate" }, { "name" : "Administrative procedures", "level" : "intermediate" }, { "name" : "State regulatory laws", "level" : "intermediate" }, { "name" : "Federal regulatory laws", "level" : "intermediate" }, { "name" : "Audit reports", "level" : "intermediate" }, { "name" : "Audit information", "level" : "intermediate" }, { "name" : "Document evaluation", "level" : "intermediate" } ], "majorSkills" : "Auditing, Contract monitoring, Compliance monitoring", "majorSkillsList" : [ "Auditing", "Contract monitoring", "Compliance monitoring" ], "coreResponsibilities" : "Plan monitoring reviews, Participate in monitoring reviews, Gather monitoring data, Track monitoring data, Assess monitoring data, File monitoring data, Utilize agency systems, Obtain contractor information, Obtain case information, Complete data entry, Develop draft reports, Develop draft correspondence", "domainKnowledge" : "Agency budgetary controls; Administrative procedures; State regulatory laws; Federal regulatory laws", "domainList" : [ "agency-budgetary-controls", "administrative-procedures", "state-regulatory-laws", "federal-regulatory-laws" ], "domainSpecificKnowledge" : [ "Agency budgetary controls", "Administrative procedures", "State regulatory laws", "Federal regulatory laws" ], "communicationSkills" : "Composing reports; Composing correspondence", "documentationSkills" : "Audit reports", "continuousLearning" : "Training opportunities; Development opportunities", "problemSolvingSkills" : "Analytical skills; Identifying areas of change; Making recommendations", "outcomesObjectives" : "Improve processes; Improve internal controls", "qualificationsBasic" : "Graduation from accredited college or university, Four years of full-time experience, License to practice as CPA in Texas, Certificate to practice as CIA, Certificate to practice as CISA", "qualificationsPreferred" : "Certified Texas Contract Manager", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "WHO WE ARE: Texas Workforce Commission connects people with careers across the state. While we are based in Austin on the north lawn of the Texas State Capitol, we have offices statewide. We're a Family Friendly Certified Workplace with great work-life balance, competitive salaries, extensive opportunities for training and development, and fantastic benefits. This position is located at 101 E. 15th St, Austin, Texas, in the Contract Oversight and Support Department. 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-motivated individual who possesses strong analytical skills, attention to detail, and excellent communication skills. A candidate well versed in auditing and monitoring practices, possessing the ability to build and maintain relationships with team members, and a commitment to upholding strong professional standard and ethics. WHAT YOU WILL DO: The Auditor I performs entry-level to routine (journey-level) auditing work. Works under moderate supervision, with limited latitude for the use of initiative and independent judgment. YOU WILL BE TRUSTED TO: -Plan for and participates in assigned monitoring reviews. -Gather, track, assess, and file monitoring-related data and information. -Utilize Agency systems to obtain relevant contractor and case information and complete monitoring-related data entry. -Develop draft monitoring reports and correspondence under the direction of a lead monitor. -Perform other duties as assigned. YOU QUALIFY WITH: - Graduation from an accredited four-year college or university with major course work in accounting, business administration, finance, economics or a related field -OR- -Four years of full-time experience in accounting, program financial performance or IT auditing, or in management information systems analysis, business process analysis, contract monitoring, or in positions which provided extensive knowledge of agency budgetary controls, or administrative procedures and related state and federal regulatory laws may substitute for education. -A license to practice as a Certified Public Accountant (CPA) in Texas will satisfy the minimum requirements. -A certificate to practice as a Certified Internal Auditor (CIA) or as a Certified Information Systems Auditor (CISA) will satisfy the minimum requirements. YOU ARE A GREAT FIT WITH: -Excellent communication skills -Experience in auditing, contract monitoring, or compliance monitoring. -Quality control or project management experience. -Proficiency in composing clear and concise audit reports, gathering and analyzing accurate and relevant audit information, and evaluating documents for accuracy and legal conformance. -Experience with identifying areas of needed change and making recommendations to improve processes and internal controls. -Certified Texas Contract Manager to assist with Contract Oversight and Support department’s work and mission. YOU GAIN: - A Family Friendly Certified Workplace. - Competitive salary: $4,650.00/month - 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_AccountingAuditingandFinance.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" : "Auditor at Texas Workforce Commission. Skills: Auditing, Contract monitoring, Compliance monitoring. Plan monitoring reviews. Participate in monitoring reviews", "createdAt" : "2026-06-14T18:48:01.510", "lastUpdated" : "2026-06-16T02:38:39.455", "ingestTimestamp" : "2026-06-14T18:48:01.510", "mongoId" : "69ec72e84c40e2acd1d0b696", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 48000, "salaryAnnualMax" : 62000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Auditing", "Financial performance", "IT auditing", "Business process analysis", "Agency budgetary controls", "Administrative procedures", "State regulatory laws", "Federal regulatory laws", "Audit reports", "Audit information", "Document evaluation", "Contract monitoring", "Compliance monitoring", "Quality control", "Project management", "Process improvement", "Internal controls", "Certified Public Accountant (CPA)", "Certified Internal Auditor (CIA)", "Certified Information Systems Auditor (CISA)", "Certified Texas Contract Manager" ], "skillCount" : 21, "jobCategory" : "finance", "jobSubcategory" : "accounting", "seniorityLevel" : "Entry", "dataQualityScore" : 0.7777778, "_score" : 621.3838, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Government", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c6ac174d8ee00a090db95", "title" : "Senior Internal Auditor", "company" : "Atlas Air Worldwide", "industry" : "Logistics", "salary" : { "min" : 87500.0, "max" : 117500.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "White Plains, NY, USA", "locations" : [ "White Plains", "NY", "USA" ], "certifications" : [ "CPA", "CIA", "Association of Chartered Certified Accountants", "Chartered Accountant" ], "timestamp" : "2026-06-15T09:39:56.561", "fingerprint" : "8347375c4930de2e907d350ec3acdc1f87aa66390984cb4e13887183d0c02de7", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://www.atlasairworldwide.com/careers/job-board/?gh_jid=4221968009", "externalId" : "4221968009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "White Plains", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "41.0339862,-73.7629097" } ], "locationText" : "White Plains, New York, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "MS Word, MS PowerPoint, MS Excel, Tableau, PowerBI, Python", "professionalSkills" : [ "Risk assessment", "Process testing", "Control testing", "Audit reporting", "Project management" ], "hardSkillsList" : [ "Data analysis", "Internal controls testing", "Risk-based audits" ], "softSkillsList" : [ "Critical thinking" ], "hardSkills" : [ { "name" : "Data analysis", "level" : "intermediate" }, { "name" : "Internal controls testing", "level" : "intermediate" }, { "name" : "Risk-based audits", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Critical thinking" } ], "majorSkills" : "Internal audit, SOX compliance, Risk assessment", "majorSkillsList" : [ "Internal audit", "SOX compliance", "Risk assessment" ], "coreResponsibilities" : "Lead daily planning and execution of global internal, Perform risk assessments, Scoping audits, Planning audits, Fieldwork, Testing, Administration of self-assessments, Reporting audit findings, Develop audit programs, Develop testing procedures, Perform detailed review and analysis over process and, Identify potential process and control gaps, Supervise and assist in the development of Internal, Prepare list of project-related audit issues, Discuss validation and remediation plan with local management, Provide brief of all audit issues to local, Prepare and share draft of audit report, Coordinate action plans to address each issue, Assist in development and implementation of data analytical, Keep IA Management informed of audit status, Maintain and update departmental policies and procedures manual, Exhibit project management skills, Hold self and others accountable to deadlines, Support multiple projects simultaneously, Manage timelines, Deliver high-quality work products, Enhance the brand and perceived value of IA, Perform activities related to internal controls certification, Execute development and maintenance of testing strategies and, Assess operating effectiveness of key controls, Identify areas for improvement, Facilitate appropriate corrective actions and remediation, Monitor progress to ensure timely remediating, Execute administration of internal controls self-assessment program, Execute fraud risk management education efforts", "teamCollaboration" : "Work with local management; Work with IA Management; Work with Staff Vice President; Cooperation among management team; Cooperation among internal audit staff", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Sarbanes-Oxley; Internal Controls; IIA Standards; COSO Integrated Frameworks; Enterprise Risk Management", "domainList" : [ "sarbanes-oxley", "internal-controls", "iia-standards", "coso-integrated-frameworks", "enterprise-risk-management" ], "domainSpecificKnowledge" : [ "Sarbanes-Oxley", "Internal Controls", "IIA Standards", "COSO Integrated Frameworks", "Enterprise Risk Management" ], "toolProficiency" : [ "MS Word", "MS PowerPoint", "MS Excel", "Tableau", "PowerBI", "Python" ], "communicationSkills" : "Written communication; Oral communication; Presentation skills", "problemSolvingSkills" : "Analytical skills", "qualificationsBasic" : "Bachelor's degree in Accounting or Internal Auditing, CPA, CIA or equivalent certificate required, Two+ years’ experience in corporate audit, accounting, public accounting or consulting, Proficiency in internal auditing principles and best practices", "qualificationsPreferred" : "Actively pursuing CPA, CIA or equivalent certificate", "workSiteFlexibility" : "Onsite", "rawDescription" : "Join Atlas Air Worldwide. Move the World with Us! At Atlas Air Worldwide, we’re not just an airline, we’re a global engine powering cargo, passenger, and leasing operations across more than 70 countries. As a leader in outsourced aviation logistics, we’re built on a foundation of safety, service excellence, integrity, innovation, teamwork, and responsibility. With over 30 years of history, a modern all-Boeing fleet, and nearly 5,000 teammates collaborating across operations, technical, and corporate functions, we’re driven by purpose. If you're ready to grow, innovate, and help us deliver excellence every single day, you belong here. Position Summary: The position is responsible for leading the daily planning and execution of the Company’s global internal audit activities in compliance with Company policies, the Internal Audit Charter and the Institute of Internal Auditors’ (“IIA”) International Standards for the Professional Practice of Internal Auditing (“Standards”). The position will provide supervision and direction of daily audit work of staff supporting risk-based audits and Sarbanes-Oxley (“SOX”) compliance. The position reports to the Senior Manager, Internal Audit (“IA”) and indirectly to the Staff Vice President of IA. Values and Behavioral Standards: To ensure the effective communication and application of company values and behavioral standards, as stated in our company “Code of Conduct” policy, and to respond appropriately in the event of any known departure. Major Job Accountabilities: INTERNAL AUDIT Work with the Senior Manager or other supervisor to perform the following: Lead the execution of all financial and operational global internal audit activities including the performance of risk assessments, scoping, planning, fieldwork, testing, administration of self-assessments, and reporting. Develop audit programs and testing procedures relevant to risk, process, controls, and test objectives. Perform detailed review and analysis over process and control documentation to identify potential process and control gaps. Supervise and assist in the development of Internal Audit staff. Prepare a list of project-related audit issues and constructively discuss validation and a remediation plan with local management. Provide a brief of all audit issues to local management for discussion during the audit closing meeting. Prepare and share a draft of the audit report with local management for discussion and coordination of their action plans to address each issue. Assist in the development and implementation of data analytical audit techniques. Keep IA Management informed of the status of audits in progress and any potential roadblocks or significant audit findings as they arise. Assist in the effort to maintain and update the comprehensive departmental policies and procedures manual that adheres to the requirements of the IIA’s Standards. Exhibit strong project management skills with the ability to hold self and others accountable to deadlines. Support multiple projects simultaneously and effectively manage timelines to deliver high-quality work products efficiently and effectively with limited supervision. Work with the Staff Vice President and Senior Manager to develop, sustain, and continuously enhance the brand and perceived value of IA within the Company. SARBANES-OXLEY/INTERNAL CONTROLS COMPLIANCE Perform activities related to internal controls certification including risk assessment, control design and test of operating effectiveness. Execute the development and maintenance of appropriate testing strategies and plans to enable management to assess the operating effectiveness of key controls over financial reporting. Constructively work with management to identify areas for improvement, collectively agree upon and facilitate appropriate corrective actions and remediation while monitoring progress to ensure the timely remediating of significant deficiencies, material weaknesses or exceptions by the Company. Execute the administration of the Company’s internal controls self-assessment program and other fraud risk management education efforts. Qualifications: Bachelor’s degree in Accounting or Internal Auditing. Holding or actively pursuing CPA, CIA or equivalent certificate (e.g., Association of Chartered Certified Accountants, Chartered Accountant, etc.) required. Two+ years’ experience in corporate audit, accounting, public accounting or consulting. Strong proficiency in internal auditing principles and best practices. Sound track record of accomplishment. Excellent oral and written communication and presentation skills, strong capacity to think critically and utilize analytical skills to support findings and recommendations, ability to maintain composure under pressure while taking a proactive approach to problem-solving; ability to demonstrate speed of accurate execution of tasks, and the overall execution of job responsibilities are all essential qualities necessary to be successful in this positi Demonstrated knowledge and understanding of Sarbanes-Oxley/Internal Controls testing requirements. Demonstrated knowledge and understanding of IIA Demonstrated knowledge of COSO Integrated Frameworks for Internal Control and Enterprise Risk Managemen Ability to provide sound business judgment and strategic thinking to enable the Company to create and sustain a “best in class” internal control function and risk assurance environment. Ability to inspire a strong spirit of cooperation among the management team and internal audit staff while embracing the Department’s philosophy of continuous process improvement and disciplined process execution. Skills Proficiency with MS Word to develop impactful audit reports. Proficiency with MS PowerPoint to create executive-level presentations. Proficiency with advanced MS Excel skills to perform data analysis. Proficiency in data analytical audit techniques (e.g., use of Tableau, PowerBI, Python). Drive adoption of AI/automation in testing by identifying opportunities to leverage analytics, scripts, or AI-based tools to streamline control testing, risk assessments, and documentation workflows. Other Requirements Ability to travel approximately 5 – 10% is required. Ability to work overtime as required. #GH19 #LI-Hybrid #LI-20 The Company is an Equal Opportunity Employer. It is our policy to afford equal employment opportunity to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, national origin, citizenship, place of birth, age, disability, protected veteran status, gender identity or any other characteristic or status protected by applicable in accordance with federal, state and local laws. If you'd like more information about your EEO rights as an applicant under the law, please download the available EEO is the Law document by clicking \"EEO Is The Law\" . To view our Pay Transparency Statement, please click here: Pay Transparency Statement Competitive compensation will be offered based on a variety of factors, including a candidate's experience, skills, education, geographic location, internal equity and other factors. In addition, a range of benefits to include medical, dental and vision insurance, employee assistance program, as well as generous paid time off, and 401K contributions are offered as a part of the total compensation package. Pay Range $87,500—$117,500 USD At Atlas Air Worldwide, we believe in the power of people, the promise of innovation, and the responsibility we hold to each other, to our customers, and to the planet. Join us and be part of a team that lifts more than cargo; we lift ambition.", "summaryDescription" : "Senior Internal Auditor at Atlas Air Worldwide. Skills: Internal audit, SOX compliance, Risk assessment. Lead daily planning and execution of global internal. Perform risk assessments", "postedDate" : "2026-06-13T21:47:57.179", "createdAt" : "2026-06-13T21:47:57.179", "lastUpdated" : "2026-06-15T09:39:56.561", "ingestTimestamp" : "2026-06-13T21:47:57.179", "mongoId" : "6a2c6ac174d8ee00a090db95", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 87500, "salaryAnnualMax" : 117500, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Data analysis", "Internal controls testing", "Risk-based audits", "Critical thinking", "Internal audit", "SOX compliance", "Risk assessment", "Process testing", "Control testing", "Audit reporting", "Project management", "Sarbanes-Oxley", "Internal Controls", "IIA Standards", "COSO Integrated Frameworks", "Enterprise Risk Management", "CPA", "CIA", "Association of Chartered Certified Accountants", "Chartered Accountant", "MS Word", "MS PowerPoint", "MS Excel", "Tableau", "PowerBI", "Python" ], "skillCount" : 26, "jobCategory" : "finance", "jobSubcategory" : "accounting", "seniorityLevel" : "Senior", "dataQualityScore" : 1.0, "_score" : 616.7284, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Logistics", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2c6c9474d8ee00a0919f68", "title" : "Medical Device Sales Territory Account Manager", "company" : "Tactile Medical", "industry" : "Healthcare", "salary" : { "min" : 87600.0, "max" : 110880.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Field", "locations" : [ "Field" ], "timestamp" : "2026-06-16T03:57:31.892", "fingerprint" : "c9044723347f03c1d67c03073b44338efe1798f8f123ad43ce8e7683b5f59e62", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/tactilemedical/jobs/4266554009", "externalId" : "4266554009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Milton", "state" : "Pennsylvania", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "41.0177269,-76.8530840" }, { "city" : "Mifflinburg", "state" : "Pennsylvania", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.9175820,-77.0477501" }, { "city" : "Selinsgrove", "state" : "Pennsylvania", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.7993524,-76.8619072" }, { "city" : "Beavertown", "state" : "Pennsylvania", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.7536190,-77.1693212" } ], "locationText" : "Milton, Pennsylvania, United States; Mifflinburg, Pennsylvania, United States; Selinsgrove, Pennsylvania, United States; Beavertown, Pennsylvania, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "coreResponsibilities" : "Educate therapists, patients, and physicians on Tactile Medical, Establish sales strategies to attain sales goals, Provide customer support with training, reimbursement, concerns, or, Maintain compliance with regulatory requirements, Assist in providing customer support, Other duties as assigned", "domainKnowledge" : "third party payer policies", "domainList" : [ "third-party-payer-policies" ], "domainSpecificKnowledge" : [ "third party payer policies" ], "specialRequirements" : "Travel within territory, Travel outside territory for conferences, Travel outside territory for training, Lift 20 pounds", "outcomesObjectives" : "Attain monthly sales goals; Attain quarterly sales goals; Attain annual sales goals; Penetrate underserved clinical markets", "qualificationsBasic" : "Bachelor's degree or equivalent combined education and work experience (4 years), 3+ years outside/inside sales experience, 1+ years medical sales experience, 4+ years patient facing clinical experience, 2+ years Tactile Medical patient facing or sales support work experience", "qualificationsPreferred" : "Healthcare sales experience with clinicians, Clinical experience with lymphedema patients, Demonstrated success selling Tactile Medical products", "workSiteFlexibility" : "Onsite", "rawDescription" : "At Tactile Medical, we specialize in developing at-home therapy devices to treat lymphedema, chronic venous insufficiency and respiratory illnesses. The Territory Account Manager is responsible for educating therapists, physicians and patients on Tactile Medical Products in an assigned territory. Responsible for establishing sales strategies to attain monthly, quarterly and annual sales goals. Responsible for penetrating underserved clinical markets. Assist in providing customer support with training, reimbursement, concerns, or complaints. Must maintain compliance with all appropriate regulatory requirements, including HIPAA. Responsibilities Educating therapists, patients, and physicians on the Flexitouch System and other products and services offered by Tactile Medical Establish sales strategies to attain monthly, quarterly, and annual sales goals Assist in providing customer support with training, reimbursement, concerns, or complaints Other duties as assigned Qualifications Education & Experience: Required: Bachelor’s degree or equivalent combined education and work experience (4 years) 3+ years of outside/inside sales experience OR 1+ years of medical sales experience OR 4+ years of patient facing clinical experience OR 2+ years of Tactile Medical patient facing or sales support work experience Preferred: Healthcare sales experience with clinicians such as doctors, surgeons, therapists, etc. Clinical experience working directly with lymphedema patients such as a Nurse, CLT, PTA, PT, OT, OTA, etc. Demonstrated success selling Tactile Medical products Knowledge & Skills: Knowledgeable of third party payer policies Demonstrated ability to launch new products desirable Travel within territory as well as outside territory for conferences and training Ability to lift 20 pounds Our total compensation package includes medical, dental and vision benefits, retirement benefits, employee stock purchase plan, paid time off, parental leave, family medical leave, volunteer time off and additional leave programs, life insurance, disability coverage, and other life and work wellness benefits and discounts. Benefits may be subject to generally applicable eligibility, waiting period, contributions, and other requirements and conditions. Below is the starting salary or hourly range for this position, although offers may differ based on the candidate's location, job-specific knowledge, skills and experience. US Pay Range $87,600—$110,880 USD To learn more about our Privacy Statement follow this link - https://tactilemedical.com/privacy-statement/ To learn more about our California Privacy Notice follow this link - https://tactilemedical.com/california-privacy-notice/", "summaryDescription" : "Medical Device Sales Territory Account Manager at Tactile Medical. Educate therapists, patients, and physicians on Tactile Medical. Establish sales strategies to attain sales goals", "postedDate" : "2026-06-14T18:34:17.980", "createdAt" : "2026-06-14T18:34:17.980", "lastUpdated" : "2026-06-16T03:57:31.892", "ingestTimestamp" : "2026-06-14T18:34:17.980", "mongoId" : "6a2c6c9474d8ee00a0919f68", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 87600, "salaryAnnualMax" : 110880, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "third party payer policies" ], "skillCount" : 1, "jobCategory" : "sales", "jobSubcategory" : "revenue", "seniorityLevel" : "Mid", "dataQualityScore" : 0.8888889, "_score" : 616.67816, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a305059f292fd229ceef4fb", "title" : "Senior Quality Manager", "company" : "Ultra", "industry" : "R&D", "salary" : { "min" : 90000.0, "max" : 115000.0, "currency" : "USD", "frequency" : "Yearly" }, "location" : "Frankfort, Kentucky", "locations" : [ "Frankfort, Kentucky" ], "certifications" : [ "CQA", "CQM", "ASQ" ], "timestamp" : "2026-06-16T08:55:52.676", "fingerprint" : "b350277debcc8baa40102edd20d5a29822e51506f554905c0f4f799661a817fb", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/ultra/52c15739-3eab-444f-b0d4-24ec56373dc3/application", "externalId" : "52c15739-3eab-444f-b0d4-24ec56373dc3", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Frankfort", "state" : "Kentucky", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "38.2009055,-84.8732836" } ], "locationText" : "Frankfort, Kentucky, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "GMP", "professionalSkills" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement", "Risk-based audit", "GMP compliance", "Sanitation assessment", "Documentation practices", "Batch record integrity", "Audit readiness", "Complaint management", "Triage criteria", "Investigation workflows", "Escalation paths", "Root-cause investigations", "Trend analyses", "Specification setting", "Stability testing", "Release testing", "Supplier qualification", "Supplier approval", "Risk assessments", "Supplier change controls", "Performance monitoring", "Quality management system", "Deviation control", "Change control" ], "hardSkillsList" : [ "CAPA", "Root-cause analysis", "Identity testing" ], "hardSkills" : [ { "name" : "CAPA", "level" : "intermediate" }, { "name" : "Root-cause analysis", "level" : "intermediate" }, { "name" : "Identity testing", "level" : "intermediate" } ], "majorSkills" : "Quality systems, Audit programs, Supplier qualification, Complaint management", "majorSkillsList" : [ "Quality systems", "Audit programs", "Supplier qualification", "Complaint management" ], "coreResponsibilities" : "Develop audit schedule, Execute audit schedule, Conduct on-site audits, Conduct remote audits, Assess GMP compliance, Assess sanitation, Assess documentation practices, Assess batch record integrity, Issue audit reports, Track corrective actions, Track preventive actions, Verify CAPA closure, Maintain audit readiness, Build consumer complaint system, Own consumer complaint system, Capture consumer complaints, Categorize consumer complaints, Track consumer complaints, Investigate consumer complaints, Respond to consumer complaints, Establish triage criteria, Establish investigation workflows, Establish escalation paths, Lead root-cause investigations, Drive CAPA to resolution, Generate trend analyses, Generate reporting, Define supplier qualification program, Administer supplier qualification program, Review Certificates of Analysis, Review specifications, Review identity testing requirements, Conduct supplier risk assessments, Approve suppliers, Disapprove suppliers, Maintain Approved Supplier List, Manage supplier change controls, Manage supplier requalification, Monitor supplier performance, Maintain quality management system, Improve quality management system, Ensure regulatory compliance, Partner with Product Development", "teamCollaboration" : "Cross-functional teams; Product Development", "domainKnowledge" : "Dietary supplements; 21 CFR Part 111; Botanical extract identity", "domainList" : [ "dietary-supplements", "21-cfr-part-111", "botanical-extract-identity" ], "domainSpecificKnowledge" : [ "Dietary supplements", "21 CFR Part 111", "Botanical extract identity" ], "documentationSkills" : "SOPs; Specifications; Batch records", "problemSolvingSkills" : "Root cause analysis", "qualificationsBasic" : "Bachelor's degree in scientific discipline, 5–7+ years in quality roles, Built or run audit programs, Built or run supplier qualification systems, Stood up complaint management systems from scratch, Stood up quality tracking systems from scratch, Investigation skills, Root-cause analysis skills", "qualificationsPreferred" : "Advanced degree a plus, 1–3+ years leadership capacity a plus, Experience with oral pouch delivery formats, Experience with buccal delivery formats, Experience with similar delivery formats, Quality certifications a plus", "remoteFriendly" : true, "workSiteFlexibility" : "Onsite", "rawDescription" : "Ultra™ | Nicotine-Free Functional Pouches About Ultra ⚡️ Ultra™ is already the #1 brand of nicotine-free pouches in the world and we only launched one year ago—we’re just getting started. Our mission is to build the category-defining brand of functional pouches for people who want enhanced performance without the crash, addiction, or long-term downsides. ULTRA doesn’t just make a pouch that’s somewhat “better for you” than Zyn—we make functional performance products that are actively good for you. The market shift is massive: nicotine pouch sales are up 3,000% since 2019 and projected to reach $20B by 2026. Consumers are adopting the pouch form factor at scale, and many are now seeking nicotine-free functional benefits. Ultra is positioned to lead that wave. Backed by some of the best investors, founders and athletes in the world, including: - CAVU Consumer Partners (Once Upon A Farm, Poppi, Farmer’s Dog, Oatly, Vital Proteins, Whoop, Recess) - Left Lane Capital (Blank Street, Olipop, Holy) - Sugar Capital (Grüns, Feastables, Lucky Energy) - Athletes & Creators: Joe Burrow, Dak Prescott, Henrik Lundqvist, Jakob Chychrun + more - Founders & Operators: Chad Janis (Grüns), Harpreet Singh (Oura Ring), Jeff Raider (Harry’s), Vinay Menda (Blank Street) + more Learn more: takeultra.com http://takeultra.com The Role \uD83D\uDE80 As Senior Quality Manager at ULTRA, you’ll own quality systems across the entire supply chain—from raw material suppliers through co-manufacturers and distributors to the end consumer. You’ll build and run the external audit program, stand up the consumer complaint management system, and establish the supplier qualification standards that ensure every pouch meets specification and regulatory requirements under 21 CFR Part 111. This is a build role. You won’t be maintaining someone else’s systems—you’ll be standing them up from scratch. If you thrive on creating structure where there is none and want to define quality for the fastest-growing pouch brand in the market, this is your opportunity. What You’ll Own \uD83D\uDCBC Co-Manufacturer Auditing - Develop and execute a risk-based audit schedule covering all co-manufacturers. - Conduct on-site and remote audits assessing GMP compliance, sanitation, documentation practices, and batch record integrity. - Issue audit reports, track corrective and preventive actions (CAPA), and verify closure within defined timelines. - Maintain audit readiness for internal facilities, including The ULTRA Compound (R&D lab). Consumer Complaint Management - Build and own an end-to-end system to capture, categorize, track, investigate, and respond to consumer complaints. - Establish triage criteria, investigation workflows, and escalation paths for adverse events and product quality issues. - Lead root-cause investigations and drive CAPA through to resolution. - Generate trend analyses and reporting to surface systemic issues and inform formulation, process, and labeling decisions. - Manage regulatory reporting obligations for serious adverse events. Supplier Qualification - Define and administer the supplier qualification and approval program for raw materials, excipients, and packaging. - Review Certificates of Analysis, specifications, and identity testing requirements, including botanical extract identity under 21 CFR Part 111. - Conduct supplier risk assessments, approve or disapprove suppliers, and maintain the Approved Supplier List. - Manage supplier change controls, requalification, and ongoing performance monitoring. Quality Systems & Compliance - Maintain and continuously improve the quality management system (SOPs, specifications, batch records, deviation and change control). - Ensure compliance with 21 CFR Part 111 and applicable dietary supplement regulations. - Partner with Product Development on specification setting, stability, and release testing. Why You’re a Fit ❓ - Bachelor’s degree in a scientific discipline (Chemistry, Food Science, Microbiology, or related); advanced degree a plus. - 5–7+ years in quality roles within dietary supplements, food, pharmaceutical, or consumer products; 1–3+ years in a leadership or management capacity a plus. - You’ve built or run audit programs and supplier qualification systems—not just maintained them. - You have working knowledge of 21 CFR Part 111, GMP, CAPA, and complaint-handling requirements. - You’ve stood up complaint management or quality tracking systems from scratch. - You’ve got strong investigation and root-cause analysis skills. - Bonus: Experience with oral pouch, buccal, or similar delivery formats. - Bonus: Quality certifications (CQA, CQM, ASQ, or equivalent). - You embody ULTRA’s values: Move fast. Be data-driven. Take ownership. Build with intention. Compete to win. Why You Should Join ULTRA \uD83D\uDCC8 - Build It from Zero. You’re not inheriting a quality system—you’re building it. Audit programs, complaint management, supplier qualification—all yours to architect. - Category-Defining Brand ULTRA is creating an entirely new category of functional pouches. You’ll define the quality bar for the brand setting the standard. - High-Performance Culture Join a team that plays to win—resourceful, detail-obsessed, and relentlessly focused on results. - Real Ownership Full responsibility over quality systems end-to-end—from supplier to consumer. Your decisions directly impact what ships. - Aligned Incentives Competitive base ($90K–$115K), equity, and a benefits package built for a team that’s going the distance. Benefits and Perks Benefits include medical, dental, and vision coverage, HSA access, a 401(k), equity, and all the Ultra pouches you could ever want. Equal Employer Opportunity Ultra is proud to be an equal opportunity workplace. We value a diverse workforce and an inclusive culture. We encourage applications from all qualified individuals regardless of race, color, religion, gender, sexual orientation, gender identity or expression, age, national origin, marital status, disability, or veteran status. We comply with all applicable employment laws, including the NYC Fair Chance Act, and provide reasonable accommodations as required by law.", "summaryDescription" : "Senior Quality Manager at Ultra. Skills: Quality systems, Audit programs, Supplier qualification, Complaint management. Develop audit schedule. Execute audit schedule", "createdAt" : "2026-06-16T00:28:24.658", "lastUpdated" : "2026-06-16T08:55:52.676", "ingestTimestamp" : "2026-06-16T00:28:24.658", "mongoId" : "6a305059f292fd229ceef4fb", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 90000, "salaryAnnualMax" : 115000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "CAPA", "Root-cause analysis", "Identity testing", "Quality systems", "Audit programs", "Supplier qualification", "Complaint management", "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement", "Risk-based audit", "GMP compliance", "Sanitation assessment", "Documentation practices", "Batch record integrity", "Audit readiness", "Triage criteria", "Investigation workflows", "Escalation paths", "Root-cause investigations", "Trend analyses", "Specification setting", "Stability testing", "Release testing", "Supplier approval", "Risk assessments", "Supplier change controls", "Performance monitoring", "Quality management system", "Deviation control", "Change control", "Dietary supplements", "21 CFR Part 111", "Botanical extract identity", "CQA", "CQM", "ASQ" ], "skillCount" : 41, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Senior", "dataQualityScore" : 0.8888889, "_score" : 616.3409, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Food & Beverage", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c7d3274d8ee00a094f3cf", "title" : "Senior Internal Auditor", "company" : "Braze", "industry" : "SaaS", "salary" : { "min" : 145000.0, "max" : 210000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Senior Internal Auditor in New York, adjusted for SaaS industry and company size." }, "location" : "New York City", "locations" : [ "New York City" ], "certifications" : [ "CPA", "CIA", "CISA" ], "timestamp" : "2026-06-15T05:40:39.142", "fingerprint" : "b3c6d5067d7819213703de73335c6c6625f87ef22ba2d35bdecedd6c3f2f4747", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://boards.greenhouse.io/braze/jobs/7993761?gh_jid=7993761", "externalId" : "7993761", "industryFunction" : { }, "structuredLocations" : [ { "city" : "New York", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.7127281,-74.0060152" } ], "locationText" : "New York, New York, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Data analysis, SQL", "professionalSkills" : [ "Risk management", "Internal controls", "Audit analytics", "Process improvement" ], "hardSkillsList" : [ "SOX compliance", "Operational audits", "Enterprise risk management", "Audit execution", "Control testing", "Remediation validation", "Risk assessments", "Business process assessment", "Automated controls", "System implementations", "Data analytics", "Continuous monitoring", "Automation", "AI-driven audit" ], "softSkillsList" : [ "Intellectually curious", "Analytical" ], "hardSkills" : [ { "name" : "SOX compliance", "level" : "intermediate" }, { "name" : "Operational audits", "level" : "intermediate" }, { "name" : "Enterprise risk management", "level" : "intermediate" }, { "name" : "Audit execution", "level" : "intermediate" }, { "name" : "Control testing", "level" : "intermediate" }, { "name" : "Remediation validation", "level" : "intermediate" }, { "name" : "Risk assessments", "level" : "intermediate" }, { "name" : "Business process assessment", "level" : "intermediate" }, { "name" : "Automated controls", "level" : "intermediate" }, { "name" : "System implementations", "level" : "intermediate" }, { "name" : "Data analytics", "level" : "intermediate" }, { "name" : "Continuous monitoring", "level" : "intermediate" }, { "name" : "Automation", "level" : "intermediate" }, { "name" : "AI-driven audit", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Intellectually curious" }, { "name" : "Analytical" } ], "majorSkills" : "SOX compliance, Internal controls, Risk management, Data analytics", "majorSkillsList" : [ "SOX compliance", "Internal controls", "Risk management", "Data analytics" ], "coreResponsibilities" : "Perform SOX testing activities, Coordinate with internal stakeholders, Monitor and validate remediation activities, Assist in execution of audits, Support audit planning activities, Assess business processes, Support Enterprise Risk Management activities, Leverage data analytics and audit tools, Support continuous monitoring initiatives, Leverage tools such as Jira, Support preparation in audit reports, Facilitate meetings, Contribute to continuous improvement", "teamCollaboration" : "Partner with stakeholders; Coordinate with external auditors; Coordinate with co-source providers; Communicate audit results", "projectManagementSkills" : [ "Agile" ], "domainKnowledge" : "SaaS environment; Subscription revenue; Professional services revenue", "domainList" : [ "saas-environment", "subscription-revenue", "professional-services-revenue" ], "domainSpecificKnowledge" : [ "SaaS environment", "Subscription revenue", "Professional services revenue" ], "toolProficiency" : [ "Jira", "Workiva", "Data analytics platforms" ], "communicationSkills" : "Executive-ready communications", "continuousLearning" : "Learning platforms; Yearly learning stipend", "problemSolvingSkills" : "Root cause analysis", "qualificationsBasic" : "B. S. in Accounting, Finance, Information Systems, 3 years minimum relevant experience, Software/SaaS or Technology industry experience, Demonstrated experience with Sarbanes-Oxley compliance, Demonstrated experience with internal controls, Demonstrated experience with risk management, Skills in data analysis, Writing SQL queries, Understanding database structures, Extracting actionable insights from complex datasets", "qualificationsPreferred" : "Professional certification such as CPA, CIA or CISA, Public Accounting or industry experience, Financial process and IT General Controls", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "At Braze, we have found our people. We’re a genuinely approachable, exceptionally kind, and intensely passionate crew. We seek to ignite that passion by setting high standards, championing teamwork, and creating work-life harmony as we collectively navigate rapid growth on a global scale while striving for greater equity and opportunity – inside and outside our organization. To flourish here, you must be prepared to set a high bar for yourself and those around you. There is always a way to contribute: Acting with autonomy, having accountability and being open to new perspectives are essential to our continued success. Our deep curiosity to learn and our eagerness to share diverse passions with others gives us balance and injects a one-of-a-kind vibrancy into our culture. If you are driven to solve exhilarating challenges and have a bias toward action in the face of change, you will be empowered to make a real impact here, with a sharp and passionate team at your back. If Braze sounds like a place where you can thrive, we can’t wait to meet you. What We’re Looking For We are seeking a Senior Internal Auditor to support and help evolve our Internal Audit function. This role is ideal for a hands-on audit professional who is eager to contribute across SOX compliance, operational audits, enterprise risk management, and audit analytics within a fast-paced, high-growth SaaS environment. Reporting to Internal Audit leadership, you will partner with stakeholders across Technology, Engineering, Finance, Legal, Security, and other business functions to evaluate risk, strengthen internal controls, and identify opportunities to improve business processes. You will play a key role in executing risk-based audit activities while helping the team leverage automation, data analytics, and continuous monitoring techniques to enhance audit effectiveness and efficiency. The ideal candidate has experience with SOX compliance, internal controls, and audit execution within a public company, public accounting, or technology-focused environment. You are intellectually curious, analytical, highly collaborative, and comfortable operating in an Agile environment. What You’ll Do Perform SOX testing activities, including walkthroughs, control testing, documentation updates, deficiency tracking, and remediation validation. Coordinate with internal stakeholders, external auditors, and co-source providers to facilitate audit execution and evidence collection. Monitor and validate remediation activities to ensure timely resolution of identified issues and control deficiencies. Assist in the execution of risk-based operational, compliance, financial, and technology audits from planning through reporting. Support audit planning activities by conducting risk assessments, gathering information, and preparing audit workpapers. Assess business processes, automated controls, and system implementations to identify control gaps and process improvement opportunities. Support quarterly Enterprise Risk Management (ERM) activities, including risk identification, risk scoring, mitigation tracking, and reporting. Leverage data analytics and audit tools to enhance testing effectiveness, identify trends, and provide actionable insights to stakeholders. Support continuous monitoring, automation, and AI-driven audit initiatives to improve audit coverage and efficiency. Leverage tools such as Jira, Workiva, and data analytics platforms to enhance audit execution, documentation, and reporting processes. Support preparation in clear and concise audit reports, presentations, and executive-ready communications that summarize risks, observations, and recommendations. Facilitate meetings, document key discussions and action items, and effectively communicate audit results to stakeholders. Contribute to the continuous improvement of Internal Audit methodologies, standards, and operational practices. Who You Are To excel in this role, you will need a combination of technical expertise, interpersonal skills, and a commitment to upholding regulatory standards. Key qualifications and attributes we're looking for include: B. S. in Accounting, Finance, Information Systems or related area Professional certification such as CPA, CIA or CISA 3 years minimum relevant experience, including Public Accounting or industry experience Software/SaaS or Technology industry experience with subscription and professional services revenue Demonstrated experience with Sarbanes-Oxley compliance, internal controls (ideally, both financial process and IT General Controls), and risk management within a corporate environment. Strong skills in data analysis, including writing SQL queries, understanding database structures, and extracting actionable insights from complex datasets. Proven track record of supporting audits, note-taking, and facilitating meetings, ideally in international settings. Strong leadership skills, high EQ and proactive problem solving approach Ability to collaborate with onshore and offshore team(s) Experience using Workiva GRC platform is a plus Experience with agile project management methodologies a plus For candidates based in the United States, the pay range for this position at the start of employment is expected to be between $79,000 and $119,000/year, with an expected On Target Earnings (OTE) between $88,000 and $132,000/year (including bonus or commission). Your exact offer may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition to cash compensation, this role qualifies for a comprehensive Total Rewards package that includes equity grants of restricted stock (RSUs) so that you will own a piece of our company. WHAT WE OFFER Braze benefits vary by location, and we encourage you to review our specific benefits offerings for each country here. More details on benefits plans will be provided if you receive an offer of employment. From offering comprehensive benefits to fostering hybrid ways of working, we’ve got you covered so you can prioritize work-life harmony. Braze offers benefits such as: Competitive compensation that may include equity Retirement and Employee Stock Purchase Plans Flexible paid time off Comprehensive benefit plans covering medical, dental, vision, life, and disability Family services that include fertility benefits and equal paid parental leave Professional development supported by formal career pathing, learning platforms, and a yearly learning stipend A curated in-office employee experience, designed to foster community, team connections, and innovation Opportunities to give back to your community, including an annual company-wide Volunteer Week and donation matching Employee Resource Groups that provide supportive communities within Braze Collaborative, transparent, and fun culture recognized as a Great Place to Work® ABOUT BRAZE Braze is the leading customer engagement platform that empowers brands to Be Absolutely Engaging™. Braze helps brands deliver great customer experiences that drive value both for consumers and for their businesses. Built on a foundation of composable intelligence, BrazeAI™ allows marketers to combine and activate AI agents, models, and features at every touchpoint throughout the Braze Customer Engagement Platform for smarter, faster, and more meaningful customer engagement. From cross-channel messaging and journey orchestration to Al-powered decisioning and optimization, Braze enables companies to turn action into interaction through autonomous, 1:1 personalized experiences. The company has been consistently recognized as a Leader in marketing technology by industry analysts, and was named a G2 “Best of Marketing and Digital Advertising Software Product” in 2026. Braze was also named a 2026 Best Places to Work by Built In, a 2025 America’s Greenest Companies by Newsweek, and a 2025 Fortune Best Workplace in Technology™ by Great Place To Work®. Braze is also proudly certified as a Great Place to Work® in the U.S., the UK, Australia, and Singapore. The company is headquartered in New York with offices in Austin, Berlin, Bucharest, Chicago, Dubai, Jakarta, London, Paris, San Francisco, São Paulo, Singapore, Seoul, Sydney and Tokyo. BRAZE IS AN EQUAL OPPORTUNITY EMPLOYER At Braze, we strive to create equitable growth and opportunities inside and outside the organization. Building meaningful connections is at the heart of everything we do, and that includes our recruiting practices. We're committed to offering all candidates a fair, accessible, and inclusive experience – regardless of age, color, disability, gender identity, marital status, maternity, national origin, pregnancy, race, religion, sex, sexual orientation, or status as a protected veteran. When applying and interviewing with Braze, we want you to feel comfortable showcasing what makes you you. We know that sometimes different circumstances can lead talented people to hesitate to apply for a role unless they meet 100% of the criteria. If this sounds familiar, we encourage you to apply, as we’d love to meet you. Please see our Candidate Privacy Policy for more information on how Braze processes your personal information during the recruitment process and, if applicable based on your location, how you can exercise any privacy rights.", "summaryDescription" : "Senior Internal Auditor at Braze. Skills: SOX compliance, Internal controls, Risk management, Data analytics. Perform SOX testing activities. Coordinate with internal stakeholders", "postedDate" : "2026-06-13T21:04:14.244", "createdAt" : "2026-06-13T21:04:14.244", "lastUpdated" : "2026-06-15T05:40:39.142", "ingestTimestamp" : "2026-06-13T21:04:14.244", "mongoId" : "6a2c7d3274d8ee00a094f3cf", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 145000, "salaryAnnualMax" : 210000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "SOX compliance", "Operational audits", "Enterprise risk management", "Audit execution", "Control testing", "Remediation validation", "Risk assessments", "Business process assessment", "Automated controls", "System implementations", "Data analytics", "Continuous monitoring", "Automation", "AI-driven audit", "Intellectually curious", "Analytical", "Internal controls", "Risk management", "Audit analytics", "Process improvement", "Agile", "SaaS environment", "Subscription revenue", "Professional services revenue", "CPA", "CIA", "CISA", "Jira", "Workiva", "Data analytics platforms" ], "skillCount" : 30, "jobCategory" : "finance", "jobSubcategory" : "accounting", "seniorityLevel" : "Senior", "dataQualityScore" : 1.0, "_score" : 616.29333, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "SaaS", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2c6c9474d8ee00a0919f69", "title" : "Medical Device Sales Territory Account Manager", "company" : "Tactile Medical", "industry" : "Healthcare", "salary" : { "min" : 73000.0, "max" : 92400.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Field", "locations" : [ "Field" ], "timestamp" : "2026-06-16T02:52:47.638", "fingerprint" : "5c5a1166866fd25d1387e660cb3b313c194b8a095901d708d9af315b6869b986", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/tactilemedical/jobs/4257244009", "externalId" : "4257244009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Milton", "state" : "Pennsylvania", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "41.0177269,-76.8530840" }, { "city" : "Mifflinburg", "state" : "Pennsylvania", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.9175820,-77.0477501" }, { "city" : "Selinsgrove", "state" : "Pennsylvania", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.7993524,-76.8619072" }, { "city" : "Beavertown", "state" : "Pennsylvania", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.7536190,-77.1693212" } ], "locationText" : "Milton, Pennsylvania, United States; Mifflinburg, Pennsylvania, United States; Selinsgrove, Pennsylvania, United States; Beavertown, Pennsylvania, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "professionalSkills" : [ "Sales strategies" ], "majorSkills" : "Sales, Customer support", "majorSkillsList" : [ "Sales", "Customer support" ], "coreResponsibilities" : "Educate therapists, patients, and physicians on products, Establish sales strategies to attain goals, Provide customer support with training, Provide customer support with reimbursement, Provide customer support with concerns, Provide customer support with complaints, Maintain compliance with regulatory requirements, Maintain compliance with HIPAA", "domainKnowledge" : "Lymphedema; Chronic venous insufficiency; Respiratory illnesses; Third party payer policies", "domainList" : [ "lymphedema", "chronic-venous-insufficiency", "respiratory-illnesses", "third-party-payer-policies" ], "domainSpecificKnowledge" : [ "Lymphedema", "Chronic venous insufficiency", "Respiratory illnesses", "Third party payer policies" ], "continuousLearning" : "Training; Conferences", "specialRequirements" : "Travel within territory, Travel outside territory, Lift 20 pounds", "outcomesObjectives" : "Attain monthly sales goals; Attain quarterly sales goals; Attain annual sales goals; Penetrate underserved clinical markets", "qualificationsBasic" : "Bachelor's degree or equivalent combined education and work experience (4 years), 3+ years of outside/inside sales experience, 1+ years of medical sales experience, 4+ years of patient facing clinical experience, 2+ years of Tactile Medical patient facing or sales support work experience", "qualificationsPreferred" : "Healthcare sales experience with clinicians, Clinical experience working directly with lymphedema patients, Demonstrated success selling Tactile Medical products", "workSiteFlexibility" : "Onsite", "rawDescription" : "At Tactile Medical, we specialize in developing at-home therapy devices to treat lymphedema, chronic venous insufficiency and respiratory illnesses. The Territory Account Manager is responsible for educating therapists, physicians and patients on Tactile Medical Products in an assigned territory. Responsible for establishing sales strategies to attain monthly, quarterly and annual sales goals. Responsible for penetrating underserved clinical markets. Assist in providing customer support with training, reimbursement, concerns, or complaints. Must maintain compliance with all appropriate regulatory requirements, including HIPAA. Responsibilities Educating therapists, patients, and physicians on the Flexitouch System and other products and services offered by Tactile Medical Establish sales strategies to attain monthly, quarterly, and annual sales goals Assist in providing customer support with training, reimbursement, concerns, or complaints Other duties as assigned Qualifications Education & Experience: Required: Bachelor’s degree or equivalent combined education and work experience (4 years) 3+ years of outside/inside sales experience OR 1+ years of medical sales experience OR 4+ years of patient facing clinical experience OR 2+ years of Tactile Medical patient facing or sales support work experience Preferred: Healthcare sales experience with clinicians such as doctors, surgeons, therapists, etc. Clinical experience working directly with lymphedema patients such as a Nurse, CLT, PTA, PT, OT, OTA, etc. Demonstrated success selling Tactile Medical products Knowledge & Skills: Knowledgeable of third party payer policies Demonstrated ability to launch new products desirable Travel within territory as well as outside territory for conferences and training Ability to lift 20 pounds Our total compensation package includes medical, dental and vision benefits, retirement benefits, employee stock purchase plan, paid time off, parental leave, family medical leave, volunteer time off and additional leave programs, life insurance, disability coverage, and other life and work wellness benefits and discounts. Benefits may be subject to generally applicable eligibility, waiting period, contributions, and other requirements and conditions. Below is the starting salary or hourly range for this position, although offers may differ based on the candidate's location, job-specific knowledge, skills and experience. US Pay Range $73,000—$92,400 USD To learn more about our Privacy Statement follow this link - https://tactilemedical.com/privacy-statement/ To learn more about our California Privacy Notice follow this link - https://tactilemedical.com/california-privacy-notice/", "summaryDescription" : "Medical Device Sales Territory Account Manager at Tactile Medical. Skills: Sales, Customer support. Educate therapists, patients, and physicians on products. Establish sales strategies to attain goals", "postedDate" : "2026-06-14T19:59:04.029", "createdAt" : "2026-06-14T19:59:04.029", "lastUpdated" : "2026-06-16T02:52:47.638", "ingestTimestamp" : "2026-06-14T19:59:04.029", "mongoId" : "6a2c6c9474d8ee00a0919f69", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 73000, "salaryAnnualMax" : 92400, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Sales", "Customer support", "Sales strategies", "Lymphedema", "Chronic venous insufficiency", "Respiratory illnesses", "Third party payer policies" ], "skillCount" : 7, "jobCategory" : "sales", "jobSubcategory" : "revenue", "seniorityLevel" : "Mid", "dataQualityScore" : 0.8888889, "_score" : 616.2163, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2c6c9474d8ee00a0919f66", "title" : "Medical Device Sales Territory Account Manager", "company" : "Tactile Medical", "industry" : "Healthcare", "salary" : { "min" : 80300.0, "max" : 101640.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Field", "locations" : [ "Field" ], "timestamp" : "2026-06-16T01:07:21.885", "fingerprint" : "6fb4391de8188acac02ef807b35a1847e2f7b893fab53c3632ee08178c4e8ebe", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/tactilemedical/jobs/4271784009", "externalId" : "4271784009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Milton", "state" : "Pennsylvania", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "41.0177269,-76.8530840" }, { "city" : "Mifflinburg", "state" : "Pennsylvania", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.9175820,-77.0477501" }, { "city" : "Selinsgrove", "state" : "Pennsylvania", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.7993524,-76.8619072" }, { "city" : "Beavertown", "state" : "Pennsylvania", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.7536190,-77.1693212" } ], "locationText" : "Milton, Pennsylvania, United States; Mifflinburg, Pennsylvania, United States; Selinsgrove, Pennsylvania, United States; Beavertown, Pennsylvania, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "professionalSkills" : [ "Sales strategies" ], "majorSkills" : "Sales, Account management", "majorSkillsList" : [ "Sales", "Account management" ], "coreResponsibilities" : "Educate therapists, patients, and physicians on Tactile Medical, Establish sales strategies to attain sales goals, Assist in providing customer support, Provide training, Handle reimbursement, Address concerns, Resolve complaints, Maintain compliance with regulatory requirements, Perform other duties as assigned", "domainKnowledge" : "Lymphedema; Chronic venous insufficiency; Respiratory illnesses; Third party payer policies", "domainList" : [ "lymphedema", "chronic-venous-insufficiency", "respiratory-illnesses", "third-party-payer-policies" ], "domainSpecificKnowledge" : [ "Lymphedema", "Chronic venous insufficiency", "Respiratory illnesses", "Third party payer policies" ], "continuousLearning" : "Conferences; Training", "specialRequirements" : "Travel within territory, Travel outside territory, Lift 20 pounds", "outcomesObjectives" : "Attain monthly sales goals; Attain quarterly sales goals; Attain annual sales goals; Penetrate underserved clinical markets", "qualificationsBasic" : "Bachelor's degree or equivalent combined education and work experience (4 years), 3+ years of outside/inside sales experience, 1+ years of medical sales experience, 4+ years of patient facing clinical experience, 2+ years of Tactile Medical patient facing or sales support work experience", "qualificationsPreferred" : "Healthcare sales experience with clinicians, Clinical experience working directly with lymphedema patients, Demonstrated success selling Tactile Medical products", "workSiteFlexibility" : "Onsite", "rawDescription" : "At Tactile Medical, we specialize in developing at-home therapy devices to treat lymphedema, chronic venous insufficiency and respiratory illnesses. The Territory Account Manager is responsible for educating therapists, physicians and patients on Tactile Medical Products in an assigned territory. Responsible for establishing sales strategies to attain monthly, quarterly and annual sales goals. Responsible for penetrating underserved clinical markets. Assist in providing customer support with training, reimbursement, concerns, or complaints. Must maintain compliance with all appropriate regulatory requirements, including HIPAA. Responsibilities Educating therapists, patients, and physicians on the Flexitouch System and other products and services offered by Tactile Medical Establish sales strategies to attain monthly, quarterly, and annual sales goals Assist in providing customer support with training, reimbursement, concerns, or complaints Other duties as assigned Qualifications Education & Experience: Required: Bachelor’s degree or equivalent combined education and work experience (4 years) 3+ years of outside/inside sales experience OR 1+ years of medical sales experience OR 4+ years of patient facing clinical experience OR 2+ years of Tactile Medical patient facing or sales support work experience Preferred: Healthcare sales experience with clinicians such as doctors, surgeons, therapists, etc. Clinical experience working directly with lymphedema patients such as a Nurse, CLT, PTA, PT, OT, OTA, etc. Demonstrated success selling Tactile Medical products Knowledge & Skills: Knowledgeable of third party payer policies Demonstrated ability to launch new products desirable Travel within territory as well as outside territory for conferences and training Ability to lift 20 pounds Our total compensation package includes medical, dental and vision benefits, retirement benefits, employee stock purchase plan, paid time off, parental leave, family medical leave, volunteer time off and additional leave programs, life insurance, disability coverage, and other life and work wellness benefits and discounts. Benefits may be subject to generally applicable eligibility, waiting period, contributions, and other requirements and conditions. Below is the starting salary or hourly range for this position, although offers may differ based on the candidate's location, job-specific knowledge, skills and experience. US Pay Range $80,300—$101,640 USD To learn more about our Privacy Statement follow this link - https://tactilemedical.com/privacy-statement/ To learn more about our California Privacy Notice follow this link - https://tactilemedical.com/california-privacy-notice/", "summaryDescription" : "Medical Device Sales Territory Account Manager at Tactile Medical. Skills: Sales, Account management. Educate therapists, patients, and physicians on Tactile Medical. 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A day in the life A typical day involves executing regression cases , raising bugs, supporting ad-hoc requests etc. Also involves interacting with QA for new features, supporting first pass and bug repro. Contributing ideas and take part in implementing them About the team Highly energetic and fun loving team with great flexibility. Team contributes to multiple aspect of the quality of E-reader devices. Handles multiple parallel releases successfully. Basic Qualifications: - Bachelor's degree - Knowledge of QA methodology and tools Preferred Qualifications: - B.E ,B.Tech. ,MSC IT and MCA - Good Communication - Testing Knowledge - Good Analytical Skill 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" : "Device Associate, Quality Services, Device Tech Support at Amazon Development Centre (India) Private Limited. Execute test plans. Create test data", "postedDate" : "2026-06-13T09:19:02.952", "createdAt" : "2026-06-13T09:19:02.952", "lastUpdated" : "2026-06-15T04:13:43.593", "ingestTimestamp" : "2026-06-13T09:19:02.952", "mongoId" : "68ed10aa70f0b99d58e7b9ec", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.com/jobs/3105257/apply", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "E-reader devices" ], "skillCount" : 1, "jobCategory" : "operations", "dataQualityScore" : 0.8888889, "_score" : 598.10956, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a2b415174d8ee00a07997ac", "title" : "Senior Device Quality Engineer", "company" : "Quality And Patient Safety", "industry" : "Healthcare", "salary" : { "min" : 135000.0, "max" : 195000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Device Quality Engineer in the US Healthcare industry, adjusted for seniority and company size." }, "location" : "United States of America", "locations" : [ "United States of America" ], "timestamp" : "2026-06-15T00:12:51.696", "fingerprint" : "5fd7eff25e79a76d1673329ce7d8c8985fec59dc6f00a5c9f74d327f250b9be1", "source" : "workday", "language" : "en", "applyUrl" : "https://gsk.wd5.myworkdayjobs.com/GSKCareers/job/USA---North-Carolina---Zebulon/Senior-Device-Quality-Engineer_442760-1", "externalId" : "442760", "industryFunction" : { }, "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "hybrid" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "ISO 14971, ISO 13485", "professionalSkills" : [ "Risk management", "Process validation", "Quality oversight", "Supplier quality management", "Device lifecycle management", "Continuous improvement", "Design changes", "Post-market quality monitoring", "Quality practices" ], "hardSkillsList" : [ "Root cause analysis", "CAPA management", "Risk management", "Process validation", "Supplier quality management", "FMEA", "8D methodology", "Statistical analysis" ], "hardSkills" : [ { "name" : "Root cause analysis", "level" : "intermediate" }, { "name" : "CAPA management", "level" : "intermediate" }, { "name" : "Risk management", "level" : "intermediate" }, { "name" : "Process validation", "level" : "intermediate" }, { "name" : "Supplier quality management", "level" : "intermediate" }, { "name" : "FMEA", "level" : "intermediate" }, { "name" : "8D methodology", "level" : "intermediate" }, { "name" : "Statistical analysis", "level" : "intermediate" } ], "majorSkills" : "Medical device quality, Risk management, Regulatory compliance", "majorSkillsList" : [ "Medical device quality", "Risk management", "Regulatory compliance" ], "coreResponsibilities" : "Ensure compliance with FDA, ISO, EU MDR, global,, Maintain risk management files, Improve risk management files, Maintain Design and Development File, Improve Design and Development File, Review technical documentation, Approve technical documentation, Review quality plans, Approve quality plans, Support new product development, Support new product introduction, Support process improvements, Support process validations, Ensure production complies with required specifications, Lead investigations for device-related nonconformances, Lead investigations for device-related deviations, Lead investigations for device-related complaints, Monitor site KPIs for device processes, Trend site KPIs for device processes, Identify risks, Support development of mitigation strategies, Lead site inspection readiness, Act as subject matter expert for regulatory inspections, Act as subject matter expert for regulatory audits, Partner with suppliers to resolve component quality issues, Partner with internal teams to resolve component quality, Support supplier quality management, Support device lifecycle management activities, Support continuous improvement, Support design changes, Support post-market quality monitoring, Support maintenance of Design and Development File, Support compliance of Design and Development File, Provide guidance to operations teams, Provide guidance to engineering teams, Provide guidance to quality teams", "teamCollaboration" : "Cross-functional teams; Internal teams; Operations teams; Engineering teams; Quality teams", "domainKnowledge" : "Medical devices; Combination products; Quality Management Systems; cGMP regulations; FDA regulations; ISO regulations; EU MDR; Design controls; Risk management; Human factors engineering; Supplier quality management", "domainList" : [ "medical-devices", "combination-products", "quality-management-systems", "cgmp-regulations", "fda-regulations", "iso-regulations", "eu-mdr", "design-controls", "risk-management", "human-factors-engineering", "supplier-quality-management" ], "domainSpecificKnowledge" : [ "Medical devices", "Combination products", "Quality Management Systems", "cGMP regulations", "FDA regulations", "ISO regulations", "EU MDR", "Design controls", "Risk management", "Human factors engineering", "Supplier quality management" ], "toolProficiency" : [ "FMEA", "8D methodology" ], "communicationSkills" : "Written communication; Verbal communication", "documentationSkills" : "Technical documentation; Design and Development Files (DDF)", "continuousLearning" : "Broaden technical skills; Career development; Personal growth; Training; Mentorship", "problemSolvingSkills" : "Root cause analysis; Investigations; Risk identification; Mitigation strategies; Problem-solving tools", "outcomesObjectives" : "Ensure products meet safety standards; Ensure products meet regulatory standards; Ensure products meet quality standards; Mitigation strategies focused on patient safety; Mitigation strategies focused on quality", "qualificationsBasic" : "Bachelor's degree in scientific, engineering, or technical discipline, 8+ years of relevant experience, Direct experience in manufacturing and quality oversight of medical devices, Hands-on experience conducting investigations, Performing root cause analysis, Managing Corrective and Preventive Action (CAPA) processes, Working knowledge of Quality Management Systems (QMS), Working knowledge of current Good Manufacturing Practice (cGMP) regulations", "qualificationsPreferred" : "Advanced degree in Engineering, Biomedical Engineering, or related discipline, Experience in management and oversight of pre-filled syringe and autoinjector assembly processes, Working knowledge of design controls, Working knowledge of risk management, Working knowledge of Design and Development File (DDF)/Design History File (DHF) requirements, Understanding of global regulations, Understanding of regulatory expectations, Understanding of inspection practices, Understanding of emerging technologies, Understanding of industry standards related to medical devices and combination products, Experience with change control, Experience with process validation, Experience with investigations, Experience with root cause analysis, Experience with CAPA management for quality and manufacturing issues, Experience with human factors engineering, Experience with device risk management, Familiarity with device-specific standards in the United States, Familiarity with regulatory requirements in the United States, Background in supplier quality management for device components, Practical experience with validation, Practical experience with verification, Practical experience with product release testing, Experience utilizing quality and problem-solving tools, Experience utilizing FMEA, Experience utilizing 8D methodology, Experience utilizing statistical analysis software", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "**Position Summary** This position ensures products meet safety, regulatory, and quality standards throughout the product lifecycle, from design and development to post-market surveillance for medical devices within combination products. Responsibilities include risk management, participation in root cause analyses, process validation, and maintaining Design and Development Files (DDF) related to medical devices. **Responsibilities** This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: * Ensure compliance with relevant FDA, ISO, EU MDR, global, and GSK requirements for medical devices within combination products. * Maintain and improve risk management files (ISO 14971) and Design and Development File (ISO 13485). * Review/Approve technical documentation, quality plans, and support new product development and introduction. * Support process improvements, validations and ensure production complies with required specifications for medical device manufacturing (filling, assembly and packaging) within combination products. * Lead investigations for device-related nonconformances, deviations, and complaints. * Monitor and trend site KPIs for device processes, identify risks, and support development of mitigation strategies focused on patient safety and quality. * Lead site inspection readiness for device related areas and act as the subject matter expert for regulatory inspections and audits. * Partner with suppliers and internal teams to resolve component quality issues and support supplier quality management. * Support device lifecycle management activities, including continuous improvement, design changes, post-market quality monitoring, and the maintenance and compliance of the Design and Development File (DDF). * Act as site Subject Matter Expert (SME) for device quality processes, providing guidance to operations, engineering, and quality teams. **Why You?** We seek clear communicators who care about quality and patient safety. You will join a collaborative team that values learning and personal growth. The role is on-site with hybrid flexibility where local site needs allow. You will have opportunities to lead projects, broaden technical skills, and influence quality practices across functions. **Basic Qualification** We are seeking professionals with the following required skills and qualifications to help us achieve our goals: * Bachelor’s degree (BA/BS) in a scientific, engineering, or technical discipline, with demonstrated medical device expertise or equivalent combination of education and experience. * Minimum of 8+ years of relevant experience in the pharmaceutical, biopharmaceutical, or related industry, including direct experience in manufacturing and quality oversight of medical devices. * Demonstrated hands-on experience conducting investigations, performing root cause analysis, and managing Corrective and Preventive Action (CAPA) processes. * Working knowledge of Quality Management Systems (QMS) and current Good Manufacturing Practice (cGMP) regulations. **Preferred Qualification** If you have the following characteristics, it would be a plus: * **Communication & Collaboration:** Strong written and verbal communication skills, with the ability to effectively collaborate and influence across cross-functional teams. * **Regulatory & Audit Support:** Experience supporting audits and regulatory inspections, including preparation, coordination, and response management. * **Device Assembly Expertise:** Preferred experience in the management and oversight of pre-filled syringe and autoinjector assembly processes. * **Design & Development Knowledge:** Working knowledge of design controls, risk management, and Design and Development File (DDF)/Design History File (DHF) requirements. * **Regulatory Knowledge:** Understanding of global regulations, regulatory expectations, inspection practices, emerging technologies, and industry standards related to medical devices and combination products. * **Quality Systems Experience:** Experience with change control, process validation, investigations, root cause analysis, and CAPA management for quality and manufacturing issues. * **Advanced Education:** Advanced degree in Engineering, Biomedical Engineering, or a related discipline preferred. * **Risk Management & Human Factors:** Experience with human factors engineering, design controls, and device risk management (e.g., ISO 14971). * **Regulatory Familiarity (U.S.):** Familiarity with device-specific standards and regulatory requirements in the United States. * **Supplier Quality:** Background in supplier quality management for device components. * **Validation & Testing:** Practical experience with validation, verification, and product release testing. * **Analytical Tools:** Experience utilizing quality and problem-solving tools such as FMEA, 8D methodology, and statistical analysis software. **Additional Info** * **Work Schedule:** This is an onsite position operating Monday through Friday, with the potential to transition to a hybrid schedule (3–4 days onsite per week) based on business needs. **What we offer** You will join a purpose-driven workplace that supports career development and well-being. We provide training, mentorship, and opportunities to grow your technical and leadership skills. We are committed to creating an inclusive environment where everyone can contribute and belong. **How to apply** We encourage you to apply if this role matches your skills and aspirations. Please submit your resume and a brief cover note outlining your relevant experience and interest in this role. We look forward to learning about you. #LI-GSK Please visit [_GSK US Benefits Summary_](http://us.gsk.com/media/7992/ustrataglance-jobpostings.pdf) to learn more about the comprehensive benefits program GSK offers US employees. **Why GSK?** **Uniting science, technology and talent to get ahead of disease together.** GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - [ _usrecruitment.adjustments @gsk.com_](mailto:usrecruitment.adjustments@gsk.com) GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. **Important notice to Employment businesses/ Agencies** GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at [_https://openpaymentsdata.cms.gov/_](https://openpaymentsdata.cms.gov/)", "summaryDescription" : "Senior Device Quality Engineer at Quality And Patient Safety. Skills: Medical device quality, Risk management, Regulatory compliance. Ensure compliance with FDA, ISO, EU MDR, global,. Maintain risk management files", "postedDate" : "2026-06-11T07:12:33.317", "createdAt" : "2026-06-12T07:12:33.245", "lastUpdated" : "2026-06-15T00:12:51.696", "ingestTimestamp" : "2026-06-12T07:12:33.245", "mongoId" : "6a2b415174d8ee00a07997ac", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://gsk.wd5.myworkdayjobs.com/GSKCareers/job/USA---North-Carolina---Zebulon/Senior-Device-Quality-Engineer_442760-1", "salaryAnnualMin" : 135000, "salaryAnnualMax" : 195000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Root cause analysis", "CAPA management", "Risk management", "Process validation", "Supplier quality management", "FMEA", "8D methodology", "Statistical analysis", "Medical device quality", "Regulatory compliance", "Quality oversight", "Device lifecycle management", "Continuous improvement", "Design changes", "Post-market quality monitoring", "Quality practices", "Medical devices", "Combination products", "Quality Management Systems", "cGMP regulations", "FDA regulations", "ISO regulations", "EU MDR", "Design controls", "Human factors engineering" ], "skillCount" : 25, "jobCategory" : "engineering", "seniorityLevel" : "senior", "dataQualityScore" : 1.0, "_score" : 589.5246, "daysOld" : 3, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare" }, { "id" : "6a2c7c6e74d8ee00a094d6d3", "title" : "Medical Review Nurse II - SNF/MDS Auditor", "company" : "Machinify", "industry" : "Healthcare", "salary" : { "min" : 85000.0, "max" : 125000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline data for a Medical Review Nurse II in the US, adjusted for mid-seniority and the healthcare industry." }, "location" : "Remote - US", "locations" : [ "Remote - US" ], "certifications" : [ "RN license" ], "timestamp" : "2026-06-16T05:25:01.680", "fingerprint" : "94afdebf6788725e8a17b1e1d7b6a8dbca3856a5083ade2059342b6b949af001", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/machinifyinc/jobs/4285261009", "externalId" : "4285261009", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "United States", "technicalSkills" : "ICD-9, ICD-10, HCPCS", "professionalSkills" : [ "Medical claims audit", "Medical review guidelines", "Audit findings documentation", "Provider education", "System edits improvement", "Audit workflow improvement", "Edit parameters establishment", "Issue packet development" ], "hardSkillsList" : [ "MDS/RAI process", "Medical records review", "Healthcare claims", "ICD-9 coding", "ICD-10 coding", "HCPCS coding", "UB-04 form application", "MDS billing process" ], "hardSkills" : [ { "name" : "MDS/RAI process", "level" : "intermediate" }, { "name" : "Medical records review", "level" : "intermediate" }, { "name" : "Healthcare claims", "level" : "intermediate" }, { "name" : "ICD-9 coding", "level" : "intermediate" }, { "name" : "ICD-10 coding", "level" : "intermediate" }, { "name" : "HCPCS coding", "level" : "intermediate" }, { "name" : "UB-04 form application", "level" : "intermediate" }, { "name" : "MDS billing process", "level" : "intermediate" } ], "majorSkills" : "MDS auditing, Medical review guidelines, Claims auditing", "majorSkillsList" : [ "MDS auditing", "Medical review guidelines", "Claims auditing" ], "coreResponsibilities" : "Perform SNF medical claims audit reviews, Conduct retrospective and prepayment audits, Audit claims for medically appropriate services, Apply appropriate medical review guidelines, Document all findings, Generate letters articulating audit findings, Support audit findings during appeals, Identify potential abuse cases, Improve medical policies, Improve provider education, Improve system edits, Keep abreast of medical practice, Keep abreast of technology changes, Keep abreast of regulatory issues, Minimize audit errors, Suggest audit workflow improvements, Assist with QA functions, Train team members, Participate in edit parameter establishment, Participate in new issue packet development, Participate in Medical Review Guidelines development, Interface with Medical Director, Support Medical Director, Cross train in clinical departments", "teamCollaboration" : "Audit team; CMD colleagues; Other contractors; Clients; Medical Director", "domainKnowledge" : "Skilled Nursing Facility; SNF; MDS; RAI process; PDPM payment methodologies; Government Payers; Commercial Payers; HIPPS codes; HIPPS Clinical Categories; RUG; LOC commercial payors; Medicare Benefit Payment Manual; Medicare Claims Processing Manual", "domainList" : [ "skilled-nursing-facility", "snf", "mds", "rai-process", "pdpm-payment-methodologies", "government-payers", "commercial-payers", "hipps-codes", "hipps-clinical-categories", "rug", "loc-commercial-payors", "medicare-benefit-payment-manual", "medicare-claims-processing-manual" ], "domainSpecificKnowledge" : [ "Skilled Nursing Facility", "SNF", "MDS", "RAI process", "PDPM payment methodologies", "Government Payers", "Commercial Payers", "HIPPS codes", "HIPPS Clinical Categories", "RUG", "LOC commercial payors", "Medicare Benefit Payment Manual", "Medicare Claims Processing Manual" ], "toolProficiency" : [ "Microsoft Office", "Word", "Excel", "PPT" ], "communicationSkills" : "Written communication; Verbal communication", "documentationSkills" : "Document findings; Create documentation", "continuousLearning" : "Keep abreast of medical practice; Keep abreast of technology changes; Keep abreast of regulatory issues", "qualificationsBasic" : "Active unrestricted RN license, Not sanctioned or excluded from Medicare, 5+ years diversified nursing experience, 1+ years MDS/RAI process experience, 1+ years medical records review experience, 1+ years healthcare claims experience, Expertise in ICD-9/ICD-10 coding guidelines, Comprehension of UB-04 form", "qualificationsPreferred" : "Experience performing utilization review, Understanding of PDPM HIPPS codes, Knowledge of RUG and LOC commercial payors", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Machinify is a leading healthcare intelligence company with expertise across the payment continuum, delivering unmatched value, transparency, and efficiency to health plan clients across the country. Deployed by over 85 health plans, including many of the top 20, and representing more than 270 million lives, Machinify brings together a fully configurable and content-rich, AI-powered platform along with best-in-class expertise. We’re constantly reimagining what’s possible in our industry, creating disruptively simple, powerfully clear ways to maximize financial outcomes and drive down healthcare costs. Please read the description and requirements carefully. This role requires specific MDS experience, so if you do not have that experience then please consider applying for one of our other Medical Review Nurse roles, which may be a better fit for you. Thank you! Job Summary: The Medical Review Nurse II - SNF/MDS primarily performs Skilled Nursing Facility (SNF) medical claims audit reviews. As a MR Nurse, you will join a team of experienced medical auditors performing retrospective and prepayment audits on claims for Government and Commercial Payers. You will work remotely in a fast-paced and dynamic environment and be part of a multi-location team. Key Responsibilities: Auditing claims for medically appropriate services provided in skilled nursing facility settings while applying appropriate medical review guidelines, policies and rules. Document all findings referencing the appropriate policies and rules. Generate letters articulating audit findings. Support audit findings during the appeals process if requested. Work collaboratively with the audit team to identify and obtain approval for particular vulnerabilities and/or cases subject to potential abuse. Work in partnership with our clients, CMD colleagues, and other contractors on improving medical policies, provider education, and system edits. Keep abreast of medical practice, changes in technology, and regulatory issues that may affect our clients. Work with the team to minimize the number of appeals; Suggest ideas that may improve audit workflows. Assist with QA functions and training team members. Participate in establishing edit parameters, new issue packets and development of Medical Review Guidelines. Interface with and support the Medical Director and cross train in all clinical departments/areas. Other duties as required to meet business needs. Knowledge, Skills and Abilities Needed: Experience with and deep knowledge of ICD-9, ICD-10, HCPCS coding. Knowledge of PDPM payment Items contributing to payment methodologies. Ability to maintain high quality work while meeting strict deadlines. Excellent written and verbal communication skills. Ability to manage multiple tasks including desk audits and claims review. Must be able to independently work within Microsoft Office products including Word, Excel, PPT, to Include creating/saving documents in folders, setting up and utilizing spreadsheets, copying and pasting data from one document to another. Must be able to manage multiple assignments effectively, create documentation outlining findings and/or documenting suggestions, organize and prioritize workload. Effectively work independently and as a team, in a remote setting. Required Qualifications: Active unrestricted RN license in good standing, is required. Must not be currently sanctioned or excluded from the Medicare program by the OIG. Minimum of five (5) years diversified nursing experience providing direct care in an inpatient or outpatient setting. One (1) or more years’ experience with MDS/ RAI process. One (1) or more years' experience performing medical records review. One (1) or more years' experience in health care claims that demonstrates expertise in ICD-9/ICD-10 coding guidelines and how it relates to the MDS RAI Process. Comprehension of the Uniform Medical Billing Form (UB-04) and application to the MDS billing process. Preferred Qualifications: Strong preference for experience performing utilization review for an insurance company, Tricare, MAC, or organizations performing similar functions. Strong preference for Understanding and in-depth comprehension of PDPM HIPPS codes including HIPPS Clinical Categories and the components that comprise the HIPPS categories. Knowledge of RUG and LOC commercial payors preferred but not required. Understanding of Medicare Benefit Payment Manual and Medicare Claims Processing Manual for SNF Equal Employment Opportunity at Machinify We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender, gender identity or expression, or veteran status. We are proud to be an equal opportunity workplace. Machinify is an employment at will employer. We participate in E-Verify as required by applicable law. In accordance with applicable state laws, we do not inquire about salary history during the recruitment process. If you require a reasonable accommodation to complete any part of the application or recruitment process, please let our recruiters know. See our Candidate Privacy Notice at: https://www.machinify.com/candidate-privacy-notice/", "summaryDescription" : "Medical Review Nurse II - SNF/MDS Auditor at Machinify. Skills: MDS auditing, Medical review guidelines, Claims auditing. Perform SNF medical claims audit reviews. Conduct retrospective and prepayment audits", "postedDate" : "2026-06-14T21:47:23.730", "createdAt" : "2026-06-14T21:47:23.730", "lastUpdated" : "2026-06-16T05:25:01.680", "ingestTimestamp" : "2026-06-14T21:47:23.730", "mongoId" : "6a2c7c6e74d8ee00a094d6d3", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 85000, "salaryAnnualMax" : 125000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "MDS/RAI process", "Medical records review", "Healthcare claims", "ICD-9 coding", "ICD-10 coding", "HCPCS coding", "UB-04 form application", "MDS billing process", "MDS auditing", "Medical review guidelines", "Claims auditing", "Medical claims audit", "Audit findings documentation", "Provider education", "System edits improvement", "Audit workflow improvement", "Edit parameters establishment", "Issue packet development", "Skilled Nursing Facility", "SNF", "MDS", "RAI process", "PDPM payment methodologies", "Government Payers", "Commercial Payers", "HIPPS codes", "HIPPS Clinical Categories", "RUG", "LOC commercial payors", "Medicare Benefit Payment Manual", "Medicare Claims Processing Manual", "RN license", "Microsoft Office", "Word", "Excel", "PPT" ], "skillCount" : 36, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.7777778, "_score" : 587.9329, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a305640f292fd229cf264ab", "title" : "AI-Native Auditor", "company" : "Modus", "industry" : "Audit", "salary" : { "min" : 75000.0, "max" : 95000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an Entry-level AI-Native Auditor in New York, Financial Services, adjusted for company size and industry." }, "location" : "New York", "locations" : [ "New York" ], "certifications" : [ "CPA", "CPA candidate" ], "timestamp" : "2026-06-16T08:06:20.472", "fingerprint" : "d41e4433af9213d7746d0950fc6f2b91c0123fd0a3086ceb80cee9180f1884a6", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/modus/1d21500c-0aa1-4eac-aebf-fa444cbac88e/application", "externalId" : "1d21500c-0aa1-4eac-aebf-fa444cbac88e", "industryFunction" : { }, "structuredLocations" : [ { "city" : "New York", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.7127281,-74.0060152" } ], "locationText" : "New York, New York, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 0, "experienceMaxYears" : 4, "experienceLevel" : "Entry", "softSkillsList" : [ "Comfortable with ambiguity" ], "softSkills" : [ { "name" : "Comfortable with ambiguity" } ], "coreResponsibilities" : "Complete audit workpapers end-to-end, Pull ready work from system, Own quality of everything shipped, Partner with reviewers, Push the product frontier, Provide feedback on tools", "teamCollaboration" : "Partnering with reviewers; Partnering with partners", "toolProficiency" : [ "Modus platform" ], "qualificationsBasic" : "0–4 years experience, CPA or CPA candidate, On track for CPA", "remoteFriendly" : true, "rawDescription" : "We're hiring AI-Native Auditors Early-career and already living in AI tools? We'll hand you our platform and let you out-produce an entire team. What You'll Do - Complete audit workpapers end-to-end, paired with our AI platform, at a speed and volume no traditional team can match - Pull ready work from Modus' practice management system tp keep engagements moving without waiting to be told what's next - Own the quality of everything you ship, partnering with reviewers and partners through sign-off - Push the product frontier — you'll be one of our heaviest users, and your feedback directly shapes the tools every Modus auditor relies on What We're Looking For - Early-career auditor (roughly 0–4 years); CPA, CPA candidate, or on track - Already living in AI tools and obsessed with using them to work faster - Comfortable with ambiguity - High-motor Why Modus Modus partners with firms by deploying purpose-built AI and growth resources to make our professionals' lives easier. We're building the future of accounting, and are looking to hire ambitious talent to help get there. ", "summaryDescription" : "AI-Native Auditor at Modus. Complete audit workpapers end-to-end. 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The Associate Territory Account Manager is responsible for selling Tactile Medical devices and educating physicians, clinicians and patients on our medical devices that are clinically proven to improve the quality of life for Lymphedema patients. Responsibilities Conducts full-cycle consultative sales (prospecting, scheduling and attending meetings, product demonstrations, in services, closing and follow-up). Works with physicians, therapists and other clinicians to increase awareness and educate on the Flexitouch System and other products and services offered by Tactile Medical Provides in-home product demonstrations on our devices for patients and assist them with questions Assists the Territory Account Manager with sales strategies and execution to surpass monthly, quarterly, and annual sales goals Assists in providing customer support through training and education in disease state, treatment protocols, reimbursement requirements, etc Compliant with all appropriate regulatory requirements, including HIPAA Other duties as assigned Qualifications Education & Experience Required: Bachelor’s degree or equivalent combined education and work experience (4 years) 1+ years of outside sales/inside sales experience OR 2+ years of patient facing clinical experience OR 1+ years of Tactile Medical patient facing or sales support work experience Preferred: Outside sales experience with in-person product demonstrations Clinical experience working directly with lymphedema patients such as a Nurse, CLT, PTA, PT, OT, OTA, etc. Demonstrated success interacting with Tactile Medical patients, customers, and clinicians Knowledge, Skills, and Abilities Excellent interpersonal, communication and time management skills Strong sales “close” experience and mentality, including persuasiveness, assertiveness and persistence Resourceful and a self-starter Ability to travel/drive within the territory as well as outside of the territory for conference, trainings, etc. Ability to lift 20 pounds Our total compensation package includes medical, dental and vision benefits, retirement benefits, employee stock purchase plan, paid time off, parental leave, family medical leave, volunteer time off and additional leave programs, life insurance, disability coverage, and other life and work wellness benefits and discounts. Benefits may be subject to generally applicable eligibility, waiting period, contributions, and other requirements and conditions. Below is the starting salary or hourly range for this position, although offers may differ based on the candidate's location, job-specific knowledge, skills and experience. US Pay Range $56,000—$74,550 USD To learn more about our Privacy Statement follow this link - https://tactilemedical.com/privacy-statement/ To learn more about our California Privacy Notice follow this link - https://tactilemedical.com/california-privacy-notice/", "summaryDescription" : "Medical Device Sales Associate Territory Account Manager at Tactile Medical. Skills: Medical device sales, Physician education, Patient education, Deal closure. Conduct full-cycle sales. 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The Associate Territory Account Manager is responsible for selling Tactile Medical devices and educating physicians, clinicians and patients on our medical devices that are clinically proven to improve the quality of life for Lymphedema patients. The geography of this territory includes the southern part of Buffalo, Orchard Park, East Aurora, Hamburg, Olean, Jamestown, Ellicottville, Warren, PA, and Bradford, PA. Responsibilities Conducts full-cycle consultative sales (prospecting, scheduling and attending meetings, product demonstrations, in services, closing and follow-up). Works with physicians, therapists and other clinicians to increase awareness and educate on the Flexitouch System and other products and services offered by Tactile Medical Provides in-home product demonstrations on our devices for patients and assist them with questions Assists the Territory Account Manager with sales strategies and execution to surpass monthly, quarterly, and annual sales goals Assists in providing customer support through training and education in disease state, treatment protocols, reimbursement requirements, etc Compliant with all appropriate regulatory requirements, including HIPAA Other duties as assigned Qualifications Education & Experience Required: Bachelor’s degree or equivalent combined education and work experience (4 years) 1+ years of outside sales/inside sales experience OR 2+ years of patient facing clinical experience OR 1+ years of Tactile Medical patient facing or sales support work experience Preferred: Outside sales experience with in-person product demonstrations Clinical experience working directly with lymphedema patients such as a Nurse, CLT, PTA, PT, OT, OTA, etc. Demonstrated success interacting with Tactile Medical patients, customers, and clinicians Knowledge, Skills, and Abilities Excellent interpersonal, communication and time management skills Strong sales “close” experience and mentality, including persuasiveness, assertiveness and persistence Resourceful and a self-starter Ability to travel/drive within the territory as well as outside of the territory for conference, trainings, etc. Ability to lift 20 pounds Our total compensation package includes medical, dental and vision benefits, retirement benefits, employee stock purchase plan, paid time off, parental leave, family medical leave, volunteer time off and additional leave programs, life insurance, disability coverage, and other life and work wellness benefits and discounts. 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