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Advanced degree preferred 8+ years of Regulatory Affairs experience within the medical device industry Demonstrated experience developing regulatory strategies for Software as a Medical Device (SaMD), digital health products, wearable technologies, or AI/ML-enabled medical technologies Strong understanding of FDA medical device regulations, regulatory pathways, and submission processes, including experience supporting or leading Q-Submissions, 510(k)s, De Novo submissions, or related regulatory interactions Working knowledge of international medical device regulations, particularly FDA and EU MDR frameworks Familiarity with AI/ML technologies, machine learning lifecycle concepts, foundation models, generative AI, and emerging regulatory approaches to artificial intelligence in healthcare Demonstrated experience partnering directly with software engineering, product management, data science, or AI/ML teams to shape product development and regulatory strategy Strong understanding of intended use, claims strategy, risk classification, software functionality, software lifecycles, and clinical evidence considerations Ability to translate complex regulatory requirements into practical guidance for product, engineering, and business stakeholders Demonstrated success influencing cross-functional teams and operating effectively in fast-paced, highly innovative environments Strong written and verbal communication skills, with the ability to clearly articulate regulatory strategy and recommendations to both technical and non-technical audiences", "summaryDescription" : "Staff Regulatory Affairs Associate (Digital Health & AI Technologies). 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We strive to enable earlier and better treatment access by bridging the gap between those searching for possible options, and the companies who develop them. We work closely with patients, healthcare professionals, trial sites, patient advocacy groups, and BioPharma – connecting key stakeholders in the drug development ecosystem.    We’ve developed a cutting-edge AI-powered technology platform that simplifies and streamlines access to drugs in development. To support our users and clients, we have a range of industry-expert specialized teams ready to help. Our services include clinical trial patient recruitment, Expanded Access Program management and Real-World Data collection.    With a global footprint spanning 134 countries, to date we’ve supported over 17,000 patients, 3,000 physicians and 350 sites, earning the trust of 60+ BioPharma companies. In October 2025, we closed a €25M investment with Avego Healthcare Capital to fuel our global ambitions and scale the business.   Join us in shaping the future of treatment access - making tomorrow’s therapies accessible for people who need them today. THE OPPORTUNITY: REGULATORY AFFAIRS DIRECTOR As Regulatory Affairs Director, you will play a critical leadership role in translating our global regulatory strategy into execution across programs, regions, and service lines. You will oversee a portfolio of regulatory activities, ensuring high-quality, compliant, and timely delivery while leading and developing a team of Regulatory Affairs professionals. You’ll work closely with cross-functional teams and act as a senior point of contact for both internal stakeholders and external partners. This role sits at the intersection of strategy, delivery, and leadership, and is key to scaling our Regulatory Affairs capabilities globally. Geographic Requirement: To ensure seamless collaboration with our teams, applicants must reside within the EST or CST time zones. WHAT YOU'LL DO IN THIS ROLE: DRIVE REGULATORY STRATEGY EXECUTION - Translate company and RA/PV strategy into clear regulatory plans across programs and regions - Drive implementation across Expanded Access Programs (EAPs), Clinical Trials, and Real-World Data initiatives OVERSEE PROGRAM AND PORTFOLIO DELIVERY - Oversee multiple regulatory programs simultaneously, ensuring delivery against timelines, quality standards, and client expectations - Identify and proactively manage cross-program risks, dependencies, and resource constraints LEAD AND DEVELOP THE TEAM - Lead, coach, and develop Regulatory Affairs Managers and senior team members - Set clear expectations and drive accountability for performance, quality, and delivery COLLABORATE CROSS-FUNCTIONALLY - Partner closely with Program Management, Medical Affairs, Quality Assurance, and Supply Chain - Ensure regulatory input is embedded into end-to-end program delivery DRIVE OPERATIONAL EXCELLENCE AND PERFORMANCE - Drive standardization, consistency, and scalability of regulatory processes - Identify improvement opportunities and implement data-driven solutions ENGAGE WITH CLIENTS AND STAKEHOLDERS - Act as a senior point of contact for clients on regulatory matters - Support client discussions, audits, and regulatory interactions with Health Authorities ENSURE QUALITY, COMPLIANCE, AND RISK MANAGEMENT - Ensure adherence to global regulatory requirements and internal processes - Support inspection readiness and audit preparedness WHAT YOU BRING TO THE TABLE: - Advanced degree in life sciences, pharmacy, or a related field - Significant experience in Regulatory Affairs within pharma, biotech, or CRO environments - Proven experience managing multiple programs and complex regulatory portfolios - Strong knowledge of global regulatory frameworks (EAP, clinical trials, or similar environments) - Demonstrated leadership experience managing teams and developing talent - Excellent stakeholder management and communication skills Equal opportunities myTomorrows is an Equal Opportunity Employer and, beyond upholding discrimination-free practices, we are committed to cultivating a workplace where difference and diversity are protected and celebrated. The best work comes from our best selves, and we go to great lengths in supporting our team members to be just that. 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Established in 2021 by proven industry leaders,", "summaryDescription" : "Director, Regulatory Affairs at Grid United", "createdAt" : "2026-06-14T21:16:27.217", "lastUpdated" : "2026-06-16T00:51:45.889", "ingestTimestamp" : "2026-06-14T21:16:27.217", "mongoId" : "6a0f51a858b93c861e05201b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 215000, "salaryAnnualMax" : 315000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Director", "dataQualityScore" : 0.7777778, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Energy", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c8cf574d8ee00a0977c5b", "title" : "Regulatory Affairs Director", "company" : "myTomorrows", "industry" : "Operations", "salary" : { "min" : 135000.0, "max" : 195000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Director of Regulatory Affairs in Amsterdam, Netherlands, adjusted for the biotech industry and company size." }, "location" : "Amsterdam HQ", "locations" : [ "Amsterdam HQ" ], "timestamp" : "2026-06-15T09:01:37.915", "fingerprint" : "4b258e93693c48fe0e86791987a687b138184c535b343c43748afa6ed9a55a45", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/mytomorrows/2dcce001-4313-4c50-b430-c9e259963e4b/application", "externalId" : "2dcce001-4313-4c50-b430-c9e259963e4b", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Amsterdam", "country" : "Netherlands", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "52.3730796,4.8924534" } ], "locationText" : "Amsterdam, Netherlands", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "professionalSkills" : [ "Regulatory strategy", "Program delivery", "Risk management", "Operational excellence", "Client engagement" ], "hardSkillsList" : [ "Regulatory affairs", "Regulatory compliance", "Health authority interactions" ], "softSkillsList" : [ "Leadership", "Mentoring" ], "hardSkills" : [ { "name" : "Regulatory affairs", "level" : "intermediate" }, { "name" : "Regulatory compliance", "level" : "intermediate" }, { "name" : "Health authority interactions", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "Regulatory strategy, Program oversight, Team leadership", "majorSkillsList" : [ "Regulatory strategy", "Program oversight", "Team leadership" ], "coreResponsibilities" : "Drive regulatory strategy execution, Translate strategy into plans, Drive implementation across EAPs, Oversee program delivery, Ensure delivery against timelines, Identify and manage risks, Lead, coach, and develop team, Set clear expectations, Drive accountability for performance, Partner with cross-functional teams, Ensure regulatory input embedded, Drive standardization of processes, Identify improvement opportunities, Implement data-driven solutions, Act as senior point of contact, Support client discussions, Support audits, Support regulatory interactions, Ensure adherence to requirements, Ensure adherence to processes, Support inspection readiness, Support audit preparedness", "teamCollaboration" : "Cross-functional teams; Program Management; Medical Affairs; Quality Assurance; Supply Chain; Clients and stakeholders", "projectManagementSkills" : [ "Program management" ], "domainKnowledge" : "Expanded Access Programs; Clinical Trials; Real-World Data", "domainList" : [ "expanded-access-programs", "clinical-trials", "real-world-data" ], "domainSpecificKnowledge" : [ "Expanded Access Programs", "Clinical Trials", "Real-World Data" ], "communicationSkills" : "Client discussions; Health Authority interactions", "problemSolvingSkills" : "Risk management", "qualificationsBasic" : "Advanced degree life sciences, Significant experience Regulatory Affairs, Experience managing multiple programs", "remoteFriendly" : true, "rawDescription" : "About myTomorrows myTomorrows is a global health tech company dedicated to breaking down barriers for patients seeking treatment options.    We strive to enable earlier and better treatment access by bridging the gap between those searching for possible options, and the companies who develop them. We work closely with patients, healthcare professionals, trial sites, patient advocacy groups, and BioPharma – connecting key stakeholders in the drug development ecosystem.    We’ve developed a cutting-edge AI-powered technology platform that simplifies and streamlines access to drugs in development. To support our users and clients, we have a range of industry-expert specialized teams ready to help. Our services include clinical trial patient recruitment, Expanded Access Program management and Real-World Data collection.    With a global footprint spanning 134 countries, to date we’ve supported over 17,000 patients, 3,000 physicians and 350 sites, earning the trust of 60+ BioPharma companies. In October 2025, we closed a €25M investment with Avego Healthcare Capital to fuel our global ambitions and scale the business.   Join us in shaping the future of treatment access - making tomorrow’s therapies accessible for people who need them today. THE OPPORTUNITY: REGULATORY AFFAIRS DIRECTOR As Regulatory Affairs Director, you will play a critical leadership role in translating our global regulatory strategy into execution across programs, regions, and service lines. You will oversee a portfolio of regulatory activities, ensuring high-quality, compliant, and timely delivery while leading and developing a team of Regulatory Affairs professionals. You’ll work closely with cross-functional teams and act as a senior point of contact for both internal stakeholders and external partners. This role sits at the intersection of strategy, delivery, and leadership, and is key to scaling our Regulatory Affairs capabilities globally. WHAT YOU'LL DO IN THIS ROLE: DRIVE REGULATORY STRATEGY EXECUTION - Translate company and RA/PV strategy into clear regulatory plans across programs and regions - Drive implementation across Expanded Access Programs (EAPs), Clinical Trials, and Real-World Data initiatives OVERSEE PROGRAM AND PORTFOLIO DELIVERY - Oversee multiple regulatory programs simultaneously, ensuring delivery against timelines, quality standards, and client expectations - Identify and proactively manage cross-program risks, dependencies, and resource constraints LEAD AND DEVELOP THE TEAM - Lead, coach, and develop Regulatory Affairs Managers and senior team members - Set clear expectations and drive accountability for performance, quality, and delivery COLLABORATE CROSS-FUNCTIONALLY - Partner closely with Program Management, Medical Affairs, Quality Assurance, and Supply Chain - Ensure regulatory input is embedded into end-to-end program delivery DRIVE OPERATIONAL EXCELLENCE AND PERFORMANCE - Drive standardization, consistency, and scalability of regulatory processes - Identify improvement opportunities and implement data-driven solutions ENGAGE WITH CLIENTS AND STAKEHOLDERS - Act as a senior point of contact for clients on regulatory matters - Support client discussions, audits, and regulatory interactions with Health Authorities ENSURE QUALITY, COMPLIANCE, AND RISK MANAGEMENT - Ensure adherence to global regulatory requirements and internal processes - Support inspection readiness and audit preparedness WHAT YOU BRING TO THE TABLE: - Advanced degree in life sciences, pharmacy, or a related field - Significant experience in Regulatory Affairs within pharma, biotech, or CRO environments - Proven experience managing multiple programs and complex regulatory portfolios - Strong knowledge of global regulatory frameworks (EAP, clinical trials, or similar environments) - Demonstrated leadership experience managing teams and developing talent - Excellent stakeholder management and communication skills Equal opportunities myTomorrows is an Equal Opportunity Employer and, beyond upholding discrimination-free practices, we are committed to cultivating a workplace where difference and diversity are protected and celebrated. 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We strive to enable earlier and better treatment access by bridging the gap between those searching for possible options, and the companies who develop them. We work closely with patients, healthcare professionals, trial sites, patient advocacy groups, and BioPharma – connecting key stakeholders in the drug development ecosystem.    We’ve developed a cutting-edge AI-powered technology platform that simplifies and streamlines access to drugs in development. To support our users and clients, we have a range of industry-expert specialized teams ready to help. Our services include clinical trial patient recruitment, Expanded Access Program management and Real-World Data collection.    With a global footprint spanning 134 countries, to date we’ve supported over 17,000 patients, 3,000 physicians and 350 sites, earning the trust of 60+ BioPharma companies. In October 2025, we closed a €25M investment with Avego Healthcare Capital to fuel our global ambitions and scale the business.   Join us in shaping the future of treatment access - making tomorrow’s therapies accessible for people who need them today. The opportunity: Regulatory Affairs & Pharmacovigilance Manager As the Regulatory Affairs and Pharmacovigilance Manager, you will be responsible for ensuring compliance of our processes with country-specific expanded access regulations globally. In this role, you'll be a key contributor to our regulatory and quality infrastructure, keeping us aligned with global legislation. You will be actively working together with Medical Affairs, Program Management, Quality Assurance, and Supply Chain and will report to the Director of Regulatory Affairs and Pharmacovigilance (Emily says hi). What you will do in this role: - Support the development and execution of regulatory strategies for Expanded Access Programs (EAPs) involving biologicals, cell therapies, and synthetic drugs. - Act as the Regulatory Affairs and Pharmacovigilance expert for communications with clients (pharmaceutical companies) and submissions to Health Authorities, as well as cross-functional meetings and audits. - Prepare, compile, and submit regulatory dossiers for cohort and named patient Expanded Access Programs (EAPs) on behalf of clients. - Provide input and support for the regulatory strategy for setting up and executing EAPs (e.g., where, when, and how). - Collaborate with the Commercial team to support new EAPs. - Ensure timely and compliant handling of all regulatory and pharmacovigilance activities related to EAPs. - Stay up to date on relevant global laws, regulations, and guidelines impacting EAPs. - Assist in drafting, reviewing, and maintaining regulatory documentation and templates. - Liaise with the Pharmacovigilance service provider to ensure alignment and compliance. - Contribute to maintaining department documentation such as SOPs (Standard Operating Procedures), QIs (Quality Incidents), and CAPAs (Corrective and Preventive Actions). What you bring to the table: - Approximately 5 years of relevant experience in Regulatory Affairs, including experience in Expanded Access. - Working knowledge of fundamental principles of Pharmacovigilance is required. - Solid understanding of national and international legislation and regulation relating to Expanded Access - A Bachelor’s or Master's degree in Life Sciences or a related field - Experience working directly with clients or external stakeholders in a professional setting - Strong communication skills (written and verbal) in English; able to convey complex topics clearly to both internal teams and external parties. Knowledge of additional languages is a plus - Comfortable collaborating across teams and working in a cross-functional environment - Proactive problem solver with the ability to identify potential regulatory or operational challenges early and suggest practical solutions - Familiarity with Microsoft 365 tools (e.g., Word, Excel, Teams, SharePoint) What we offer: - Impactful work that helps patients gain access to potentially lifesaving treatments. - International work environment, scale-up energy and flat organizational structure which encourages creativity and accountability. - Competitive salary, annual performance bonus and an Employee Stock Option Plan. - Great career development opportunities in a fast-growing company. - Learning and development budget alongside internal knowledge sharing sessions. - Hybrid working model if you're in the Netherlands. - Policies to support working parents. - Healthy lunch at the thriving Amsterdam office. - Unlimited access to professional guidance by certified psychologists via OpenUp - Enjoy monthly events hosted by our vibrant Culture Club as well as an annual ‘myTomorrowland’ company-wide celebration! Equal opportunities myTomorrows is an Equal Opportunity Employer and, beyond upholding discrimination-free practices, we are committed to cultivating a workplace where difference and diversity are protected and celebrated. The best work comes from our best selves, and we go to great lengths in supporting our team members to be just that. ", "summaryDescription" : "Regulatory Affairs Pharmacovigilance Manager at myTomorrows. Skills: Pharmacovigilance, Regulatory affairs, Risk management. Manage and oversee pharmacovigilance activities. Ensure compliance with global regulatory requirements", "createdAt" : "2026-06-14T20:12:02.438", "lastUpdated" : "2026-06-16T02:09:59.455", "ingestTimestamp" : "2026-06-14T20:12:02.438", "mongoId" : "6a2c8cf574d8ee00a0977c4f", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ "Regulatory submissions", "GVP modules", "Signal detection", "Case processing", "Aggregate reporting", "Pharmacovigilance", "Regulatory affairs", "Risk management", "Compliance oversight", "Legal analysis", "Global regulatory requirements", "Drug safety", "Clinical development" ], "skillCount" : 13, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Manager", "dataQualityScore" : 0.8888889, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c7de674d8ee00a0951298", "title" : "Senior Associate – Regulatory Affairs (EU-OTC)", "company" : "ClinChoice", "industry" : "Pharma", "salary" : { "min" : 1500000.0, "max" : 2500000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Associate – Regulatory Affairs in India, adjusted for mid-seniority, pharma industry, and company size." }, "location" : "India", "locations" : [ "India" ], "timestamp" : "2026-06-15T07:40:41.607", "fingerprint" : "0c365df45657c3f5697e3cf5573b07095ff6a6a2405e6f56b66a06e928917f4d", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.eu.greenhouse.io/clinchoice/jobs/4896340101", "externalId" : "4896340101", "industryFunction" : { }, "structuredLocations" : [ { "country" : "India", "continent" : "as", "workMode" : "onsite" } ], "locationText" : "India", "minimumEducation" : "Bachelor's", "experienceMinYears" : 4, "experienceMaxYears" : 5, "experienceLevel" : "Senior", "professionalSkills" : [ "Risk management", "Legal analysis", "Compliance oversight" ], "hardSkillsList" : [ "Regulatory affairs", "Submission management", "Regulatory documentation", "Regulatory review", "Regulatory action items", "License tracking", "Consolidated CFI review", "Aggregate report review" ], "softSkillsList" : [ "Critical thinking" ], "hardSkills" : [ { "name" : "Regulatory affairs", "level" : "intermediate" }, { "name" : "Submission management", "level" : "intermediate" }, { "name" : "Regulatory documentation", "level" : "intermediate" }, { "name" : "Regulatory review", "level" : "intermediate" }, { "name" : "Regulatory action items", "level" : "intermediate" }, { "name" : "License tracking", "level" : "intermediate" }, { "name" : "Consolidated CFI review", "level" : "intermediate" }, { "name" : "Aggregate report review", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Critical thinking" } ], "majorSkills" : "Regulatory affairs, Submission support, Renewal support, CFI support", "majorSkillsList" : [ "Regulatory affairs", "Submission support", "Renewal support", "CFI support" ], "coreResponsibilities" : "Support submission management, Support registration of OTC drugs, Compile submission packages, Prepare cover letter, Prepare application form, Prepare Module 1 documents, Compile regulatory documentation, Manage regulatory action items, Map regulatory inputs, Coordinate regulatory inputs, Plan regulatory timing, Develop project implementation plans, Manage workload planning, Ensure on-time completion, Review submission documents, Verify submission packages, Update submission trackers, Track licenses, Track approval validity, Track renewal timelines, Plan renewal submission, Coordinate renewal documentation, Submit renewal to health authority, Perform post submission activity, Review consolidated CFI, Edit consolidated CFI, Apply critical thinking, Apply common sense, Ensure regulatory actions fit purpose, Write regulatory actions, Copy regulatory actions into report, Challenge LOC contributions, Review regulatory contribution, Submit PSUSA, Follow PSUSA until completion, Submit post PSUSA variations", "teamCollaboration" : "Regional RA team; Cross-functional teams; Local RA lead; Cross-functional team", "projectManagementSkills" : [ "Workload planning" ], "domainKnowledge" : "EU-OTC drugs; EMEA regulations; PSUSA submissions", "domainList" : [ "eu-otc-drugs", "emea-regulations", "psusa-submissions" ], "domainSpecificKnowledge" : [ "EU-OTC drugs", "EMEA regulations", "PSUSA submissions" ], "toolProficiency" : [ "J tracker", "HAQ tracker", "PSMF tracker" ], "communicationSkills" : "Prepare cover letter; Prepare application form", "documentationSkills" : "Regulatory documentation; Module 1 documents; Aggregate report", "problemSolvingSkills" : "Critical thinking", "outcomesObjectives" : "Ensure on-time completion of projects; Ensure on-time completion of tasks", "qualificationsBasic" : "B.S. Chemistry, B.S. Biology, 4 years experience, 5 years experience, Regulatory Affairs experience", "rawDescription" : "Submission support: Submission management support for MRP & DCP procedures, PSUSA submission, Renewals, Repeat use procedures, variations etc. Support for the registration of OTC drugs in EU countries. Support regional RA team to compile submission packages. Prepare cover letter, application form and relevant Module 1 documents for variations. Preparation and compilation of regulatory documentation for the registration, variation and renewal of OTC drugs for EMEA. Manage regulatory action item (task) tables including mapping, coordination of regulatory inputs, and timing. Work with regional regulatory team to develop project implementation plans and manage workload planning to ensure on-time completion of projects and tasks. Regulatory review of submission documents for compliance. Work with cross-functional teams or LRA’s for submission documents and verification of packages. Updating relevant submission tracker i. e. J tracker, HAQ tracker, PSMF tracker etc. Renewal support: Tracking of licenses for registration and approval. Tracking of approval validity of licenses and renewal timelines. Planning for renewal submission. Co-ordination with cross-functional team for Renewal documentation. Co-ordination with Local RA lead for Renewal documentation and submission. Preparation of Renewal package. Submission of Renewal to health authority and post submission activity. CFI support: Review and edit the consolidated CFI independently and with applying critical thinking and common sense Make sure that all the regulatory actions provided in the consolidated CFI fit for purpose (i. e. meet requirements of GVP module VII.B.5.1 to 4) and are written in such a way that it can be directly copied into the aggregate report Challenge LOC if their contribution is not appropriate Review the regulatory contribution in the draft and final aggregate report based on the outcome of the consolidated CFI Submit the PSUSA and follow until completion Submit the post PSUSA variations Experience/Qualifications: Minimum B. S. Chemistry, Biology, or related fields Minimum of 4 ~ 5 years of experience working within a Regulatory Affairs Department (e.g., pharmaceutical, cosmetic, food supplements, etc.), with direct accountability for deliverables or a combination of direct Regulatory Affairs experience and specific interactions with a Regulatory Affairs Department by providing source documentation to CMC, Quality, or Regulatory Operations.", "summaryDescription" : "Senior Associate – Regulatory Affairs (EU-OTC) at ClinChoice. Skills: Regulatory affairs, Submission support, Renewal support, CFI support. Support submission management. Support registration of OTC drugs", "postedDate" : "2026-06-13T21:04:52.153", "createdAt" : "2026-06-13T21:04:52.153", "lastUpdated" : "2026-06-15T07:40:41.607", "ingestTimestamp" : "2026-06-13T21:04:52.153", "mongoId" : "6a2c7de674d8ee00a0951298", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Regulatory affairs", "Submission management", "Regulatory documentation", "Regulatory review", "Regulatory action items", "License tracking", "Consolidated CFI review", "Aggregate report review", "Critical thinking", "Submission support", "Renewal support", "CFI support", "Risk management", "Legal analysis", "Compliance oversight", "Workload planning", "EU-OTC drugs", "EMEA regulations", "PSUSA submissions", "J tracker", "HAQ tracker", "PSMF tracker" ], "skillCount" : 22, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Mid", "dataQualityScore" : 0.8888889, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Pharma", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2ec03f74d8ee00a0e9de38", "title" : "Associate Director, Global Regulatory Affairs, Precision Medicine & Digital Health", "company" : "Takeda", "industry" : "Pharma", "salary" : { "min" : 154400.0, "max" : 242550.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "United States of America", "locations" : [ "United States of America" ], "timestamp" : "2026-06-16T05:44:53.484", "fingerprint" : "43ff171a3133b0ca2c75fc1f5b901d1b262e67ac9ebf3aa37d836761a9893509", "source" : "workday", "language" : "en", "applyUrl" : "https://takeda.wd3.myworkdayjobs.com/External/job/Massachusetts---Virtual/Associate-Director--Global-Regulatory-Affairs--Precision-Medicine---Digital-Health_R0181968", "externalId" : "R0181968", "industryFunction" : { }, "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s [Privacy Notice](https://jobs.takeda.com/privacynotice) and [Terms of Use](https://www.takeda.com/terms-and-conditions/). I further attest that all information I submit in my employment application is true to the best of my knowledge. ## **Job Description** **Job Description** ** _Objective / Purpose_** * Provides strategic and tactical guidance to teams for the delivery of global regulatory strategies to support development and commercialization of biomarkers, diagnostic tests, devices and digital health tools to enhance the value of our products across therapeutic areas and to ensure goals/objectives are met **Accountabilities** * Responsible for developing and leading the global regulatory strategies for precision medicine and digital health efforts for assigned programs. * Identifies regulatory requirements and provides regulatory guidance, and expertise to global development team on the assigned project(s) of responsibility. * Partner with local/regional regulatory representatives to lead and support lifecycle management regulatory activities for the digital health and precision medicine portfolio, including change impact assessments, regulatory strategy alignment, and execution of required maintenance submissions/notifications to ensure ongoing compliance across markets. * Ensures therapeutic asset’s global regulatory plans effectively accommodate appropriate precision medicine approaches by effectively integrating drug and diagnostic regulatory and submission plans including HA engagement plans and mitigation strategies * Ensures line management and key stakeholders are apprised of developments that may impact regulatory success, exercising sound judgement and communicating in a professional and timely manner. * Demonstrates ability to anticipate risks and responsible for developing solutions to identified risks and discussing with management; understands probabilities of technical success for the solutions. * Effectively represent the Global Regulatory Affairs (GRA) function in senior level interactions at internal governance technical review committees, key global health authority meetings and with external partners. * Participates with influence in or leads departmental and cross-functional task-forces and initiatives. * Influence cross-functional colleagues within the therapeutic area, across GRA and across the enterprise. * Provide training to cross-functional teams to enhance their understanding of regulatory requirements and processes. * Helps implement a culture of continuous improvement to improve regulatory processes, and drive the adoption of innovation and best practices within the regulatory function. * Provide regulatory strategy support to diligence for licensing opportunities as appropriate, including regulatory input on the selection, governance, and ongoing management of device/diagnostic partners. * Monitor and anticipate trends that impact both the regulatory and access environments to strengthen product development plan(s) and adopt regulatory strategies in a timely manner. * Support external influencing activities by coordinating and contributing to regulatory/policy engagement efforts, including drafting and reviewing guidance comments and supporting trade association working groups. **_Education & Competencies (Technical and Behavioral) _** * Bachelor’s Degree, scientific discipline strongly preferred * Advanced degree in a scientific discipline (PhD., M.D., PharmD, MS) strongly preferred * A minimum of 5 years of experience in regulatory affairs. Experience working with medical devices and/or diagnostics within the pharmaceutical industry strongly preferred. * Proven track record in developing and managing regulatory strategies for digital health products, and/or diagnostics, and precision medicine. * Expert knowledge of device development, registration and maintenance requirements with experience in championing innovation in technical areas. * Comprehensive understanding of biomarker strategies and implications for drug development. * Demonstrated track record of successful interactions with FDA, EMA, Notified Bodies, and other global health authorities specifically related to Device submissions (i.e., IND, SRDs, IDEs, CTA, IMPD, BLA, MAA, NDA, 510K, CE Mark submissions and their amendments/supplements). * Understanding of scientific principles and device regulatory requirements relevant to global drug development and post-market support, including EU MDR and IVDR. * Understands and interprets scientific data as it relates to regulatory requirements and strategy for assigned projects and provides knowledge and expertise to guide team in established and building appropriate global regulatory strategy. * Demonstrates strong verbal and written communication skills, with the ability to translate complex regulatory concepts into clear, stakeholder-tailored communication **Location:** Remote within the US **Takeda Compensation and Benefits Summary** We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. **For Location:** Massachusetts - Virtual **U.S. Base Salary Range:** $154,400.00 - $242,550.00 The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location. U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. ** _EEO Statement_** _Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law._ ## **Locations** Massachusetts - Virtual ## **Worker Type** Employee ## **Worker Sub-Type** Regular ## **Time Type** Full time **Job Exempt** Yes It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.", "summaryDescription" : "Associate Director, Global Regulatory Affairs, Precision Medicine & Digital Health at Takeda", "postedDate" : "2026-06-11T21:08:41.692", "createdAt" : "2026-06-14T21:08:41.640", "lastUpdated" : "2026-06-16T05:44:53.484", "ingestTimestamp" : "2026-06-14T21:08:41.640", "mongoId" : "6a2ec03f74d8ee00a0e9de38", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://takeda.wd3.myworkdayjobs.com/External/job/Massachusetts---Virtual/Associate-Director--Global-Regulatory-Affairs--Precision-Medicine---Digital-Health_R0181968", "salaryAnnualMin" : 154400, "salaryAnnualMax" : 242550, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "executive", "dataQualityScore" : 0.8888889, "daysOld" : 4, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Pharma", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2a5d7f74d8ee00a06192ae", "title" : "Associate, Regulatory Affairs", "company" : "ClinChoice", "industry" : "Healthcare", "salary" : { "min" : 4500000.0, "max" : 7500000.0, "currency" : "AMD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Junior Regulatory Affairs Associate in Armenia, adjusted for the biotech industry." }, "location" : "Armenia", "locations" : [ "Armenia" ], "timestamp" : "2026-06-14T21:30:16.192", "fingerprint" : "3a7629cc490b7b7a32842926e3ba14c1575f4b32d1c2a4f2503118168e745418", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.eu.greenhouse.io/clinchoice/jobs/4890364101", "externalId" : "4890364101", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Armenia", "continent" : "as", "workMode" : "onsite" } ], "locationText" : "Armenia", "minimumEducation" : "Bachelor's", "professionalSkills" : [ "Regulatory submission", "Product registration" ], "hardSkillsList" : [ "Regulatory affairs", "Product labeling" ], "softSkillsList" : [ "Teamwork" ], "hardSkills" : [ { "name" : "Regulatory affairs", "level" : "intermediate" }, { "name" : "Product labeling", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Teamwork" } ], "majorSkills" : "Regulatory affairs, Marketing authorization", "majorSkillsList" : [ "Regulatory affairs", "Marketing authorization" ], "coreResponsibilities" : "Support new application for marketing authorization, Support renewal of medicinal products, Support variation of medicinal products, Support medical devices submission, Support cosmetics submission, Support food supplements submission, Follow up on queries from HA, Publish registration applications, Submit registration applications, Coordinate activities for product registration, Ensure product registration information is accurate, Ensure product registration information is current, Support compilation of regulatory information, Support tracking of regulatory information, Support indexing of regulatory information, Support archival of regulatory information, Specify storage requirements for regulated products, Specify labelling requirements for regulated products, Specify packaging requirements for regulated products, Create product labels, Update product labels, Review product labels, Quality check product labels", "teamCollaboration" : "Excellent teamwork", "domainKnowledge" : "Medicinal products; Medical devices; Cosmetics; Food supplements; Health Authority queries", "domainList" : [ "medicinal-products", "medical-devices", "cosmetics", "food-supplements", "health-authority-queries" ], "domainSpecificKnowledge" : [ "Medicinal products", "Medical devices", "Cosmetics", "Food supplements", "Health Authority queries" ], "documentationSkills" : "Regulatory information archival", "continuousLearning" : "Full performance and development process; End of year reviews; Continuous training", "qualificationsBasic" : "Bachelor's Degree in Life Science", "qualificationsPreferred" : "Experience in the related field", "workSiteFlexibility" : "Flexible", "rawDescription" : "ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house team as an Associate, Regulatory Affairs on a permanent basis. Join our team: you can be part of making a difference in peoples’ lives and experience a fulfilling and rewarding career! Main Job Tasks and Responsibilities: Support with new application for marketing authorization/renewal/variation of medicinal products, medical devices, cosmetics, food supplements for regulatory submission and follow-up closely on queries from HA through to approval Publishing and submission of products registration applications Coordination of activities ensuring product registration information is accurate and current Support compilation, tracking, indexing and archival of regulatory information Specifying storage, labelling and packaging requirements for regulated products Creation, update, review and quality check of product labels Education and Experience: Bachelor’s Degree in Life Science (Chemistry, Biology, Biomedical Engineering) Experience in the related field is a plus Fluency in English Ability to work under pressure to meet the deadlines Ability to get a challenge and perform excellent teamwork Our Benefits: Flexible Working Hours Full performance and development process with end of year reviews Team events and end of year party Employee satisfaction survey - your feedback is important for continuous improvement Health Insurance The Application Process Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. Who will you be working for? About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. We are on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Join our passionate team and make a meaningful impact on global healthcare! Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.", "summaryDescription" : "Associate, Regulatory Affairs at ClinChoice. Skills: Regulatory affairs, Marketing authorization. Support new application for marketing authorization. Support renewal of medicinal products", "postedDate" : "2026-06-11T21:19:12.696", "createdAt" : "2026-06-11T21:19:12.696", "lastUpdated" : "2026-06-14T21:30:16.192", "ingestTimestamp" : "2026-06-11T21:19:12.696", "mongoId" : "6a2a5d7f74d8ee00a06192ae", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Regulatory affairs", "Product labeling", "Teamwork", "Marketing authorization", "Regulatory submission", "Product registration", "Medicinal products", "Medical devices", "Cosmetics", "Food supplements", "Health Authority queries" ], "skillCount" : 11, "jobCategory" : "other", "jobSubcategory" : "regulatory-affairs", "dataQualityScore" : 0.7777778, "daysOld" : 3, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare" }, { "id" : "6a2c7de674d8ee00a095129b", "title" : "Senior Associate/Strategist – Regulatory Affairs (APAC CMC)", "company" : "ClinChoice", "industry" : "Pharma", "salary" : { "min" : 2200000.0, "max" : 3500000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Associate/Strategist in the Pharma industry in India, adjusted for seniority and company size." }, "location" : "India", "locations" : [ "India" ], "timestamp" : "2026-06-15T09:36:23.363", "fingerprint" : "5d111d51c069efbd5703cb08553581f513ce644d603a506de60bb09e2f7b4344", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.eu.greenhouse.io/clinchoice/jobs/4896358101", "externalId" : "4896358101", "industryFunction" : { }, "structuredLocations" : [ { "country" : "India", "continent" : "as", "workMode" : "onsite" } ], "locationText" : "India", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 5, "experienceMaxYears" : 9, "experienceLevel" : "Senior", "professionalSkills" : [ "Regulatory affairs", "Technical writing", "Editing", "Project management", "Risk management" ], "hardSkillsList" : [ "Regulatory submissions", "CMC sections", "Health Authority questions", "Regulatory compliance", "ICH guidelines", "Quality control", "Scientific data", "Regulatory documentation", "Medicinal products", "Submission approvals" ], "hardSkills" : [ { "name" : "Regulatory submissions", "level" : "intermediate" }, { "name" : "CMC sections", "level" : "intermediate" }, { "name" : "Health Authority questions", "level" : "intermediate" }, { "name" : "Regulatory compliance", "level" : "intermediate" }, { "name" : "ICH guidelines", "level" : "intermediate" }, { "name" : "Quality control", "level" : "intermediate" }, { "name" : "Scientific data", "level" : "intermediate" }, { "name" : "Regulatory documentation", "level" : "intermediate" }, { "name" : "Medicinal products", "level" : "intermediate" }, { "name" : "Submission approvals", "level" : "intermediate" } ], "majorSkills" : "Regulatory Affairs, CMC Regulatory, Technical Writing", "majorSkillsList" : [ "Regulatory Affairs", "CMC Regulatory", "Technical Writing" ], "coreResponsibilities" : "Author regulatory submissions, Review CMC sections, Ensure regulatory compliance, Collaborate with SMEs, Gather information, Maintain document quality, Manage timelines, Identify CMC regulatory issues, Propose mitigation strategies, Interpret regulations, Guide teams on regulations, Expedite submission, Obtain approvals", "teamCollaboration" : "Subject matter experts; Scientists; Quality assurance; Manufacturing teams; Regulatory affairs colleagues; Cross-functional teams", "projectManagementSkills" : [ "Manage projects" ], "domainKnowledge" : "APAC CMC; New Drug Applications; Marketing Authorization Applications; Global regions; Manufacture of medicinal products; Control of medicinal products", "domainList" : [ "apac-cmc", "new-drug-applications", "marketing-authorization-applications", "global-regions", "manufacture-of-medicinal-products", "control-of-medicinal-products" ], "domainSpecificKnowledge" : [ "APAC CMC", "New Drug Applications", "Marketing Authorization Applications", "Global regions", "Manufacture of medicinal products", "Control of medicinal products" ], "toolProficiency" : [ "ECTD format" ], "communicationSkills" : "Communication skills; Technical writing; Editing", "documentationSkills" : "Regulatory documentation; CMC sections", "problemSolvingSkills" : "Identify potential CMC Regulatory issues; Propose mitigation strategies", "outcomesObjectives" : "Timely completion of submissions", "qualificationsBasic" : "Bachelor's degree or higher, 5-9 years relevant experience, Authoring CMC sections, Technical writing expertise, Knowledge of CMC regulatory requirements, Experience with eCTD format", "qualificationsPreferred" : "Background in pharmaceutical manufacturing, Background in quality control", "rawDescription" : "Responsibilities: Authoring regulatory submissions: Writing and reviewing the CMC sections for new e. g. New Drug Applications (NDAs), and Marketing Authorization Applications (MAAs) and lifecycle maintenance regulatory filings including responses to Health Authority’s questions. Ensuring regulatory compliance: Making sure that all documents align with the requirements of regulatory bodies as well as International Council for Harmonisation (ICH) guidelines. Collaborating with subject matter experts (SMEs): Working closely with scientists, quality assurance (QA), manufacturing teams, and regulatory affairs colleagues to gather accurate and complete information about a drug's composition, manufacturing process, and quality control. Maintaining document quality: Ensuring completion of high-quality documents i. e. clear, concise, scientifically accurate, and consistent in style and format, complying with regulatory guidelines and internal processes within timelines. Managing timelines: Adhering to strict project schedules to ensure timely completion of submissions. Identify, Assess and Communicate potential CMC Regulatory issues and propose mitigation strategies. Understands, interprets and guides teams on regulations and policies related to manufacture and control of medicinal products to expedite the submission, review and obtain approvals. Essential skills and qualifications Educational background: A bachelor's degree or higher in a scientific field, such as Chemistry, Pharmaceutical Sciences, or a related discipline. Experience: Minimum of 5 ~ 9 years of relevant work experience working within a Regulatory Affairs Department with direct accountability for deliverables. Pharmaceutical experience: Prior experience authoring CMC sections for regulatory submissions is a standard requirement. Technical writing expertise: Exceptional technical writing, editing, and communication skills are required to translate complex scientific data into clear regulatory documentation. Regulatory knowledge: A strong knowledge of CMC regulatory requirements for multiple global regions (e.g., APAC, U.S., EU) is essential. Experience with the electronic Common Technical Document (eCTD) format is also crucial. Industry familiarity: A background in pharmaceutical manufacturing or quality control is often beneficial. Collaboration and project management: The ability to work independently, manage projects, and communicate effectively with cross-functional teams is critical. Detail-oriented: Meticulous attention to detail is necessary to ensure the accuracy and completeness of submissions.", "summaryDescription" : "Senior Associate/Strategist – Regulatory Affairs (APAC CMC) at ClinChoice. Skills: Regulatory Affairs, CMC Regulatory, Technical Writing. Author regulatory submissions. Review CMC sections", "postedDate" : "2026-06-14T03:07:56.137", "createdAt" : "2026-06-14T03:07:56.137", "lastUpdated" : "2026-06-15T09:36:23.363", "ingestTimestamp" : "2026-06-14T03:07:56.137", "mongoId" : "6a2c7de674d8ee00a095129b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Regulatory submissions", "CMC sections", "Health Authority questions", "Regulatory compliance", "ICH guidelines", "Quality control", "Scientific data", "Regulatory documentation", "Medicinal products", "Submission approvals", "Regulatory Affairs", "CMC Regulatory", "Technical Writing", "Regulatory affairs", "Technical writing", "Editing", "Project management", "Risk management", "Manage projects", "APAC CMC", "New Drug Applications", "Marketing Authorization Applications", "Global regions", "Manufacture of medicinal products", "Control of medicinal products", "ECTD format" ], "skillCount" : 26, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Senior", "dataQualityScore" : 1.0, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Pharma", "llmIndustryConfidence" : 0.95 }, { "id" : "6a30511af292fd229cefa721", "title" : "Staff Global Regulatory GPO", "industry" : "Legal", "salary" : { "min" : 140000.0, "max" : 170000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "US", "locations" : [ "US" ], "timestamp" : "2026-06-16T11:38:47.419", "fingerprint" : "cbdf163eae67a9f5bbfeb4a2bdbd0902da6668a8e488816cdb4d248cba5c0e38", "source" : "lever", "language" : "en", "applyUrl" : "https://jobs.lever.co/jobgether/b9326de0-f3f6-4d4d-bfdc-7cecd9141afb/apply", "externalId" : "b9326de0-f3f6-4d4d-bfdc-7cecd9141afb", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Ireland", "continent" : "eu", "workMode" : "remote" }, { "continent" : "eu", "workMode" : "remote" } ], "locationText" : "Ireland", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 4, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Regulatory strategy", "Lifecycle management", "Labeling governance", "Promotional material governance", "Regulatory workflows", "Regulatory procedures", "Marketing material review", "Advertising material review", "Promotional material review", "Training material review", "Regulatory readiness", "Compliance assessments", "Regulatory guidance development", "Stakeholder presentations", "Matrixed environments", "Global environments", "Leadership", "Influence", "Decision-making" ], "hardSkillsList" : [ "Product registration", "Global labeling requirements", "International regulations", "Internal standards", "Applicable regulatory requirements", "Global compliance" ], "hardSkills" : [ { "name" : "Product registration", "level" : "intermediate" }, { "name" : "Global labeling requirements", "level" : "intermediate" }, { "name" : "International regulations", "level" : "intermediate" }, { "name" : "Internal standards", "level" : "intermediate" }, { "name" : "Applicable regulatory requirements", "level" : "intermediate" }, { "name" : "Global compliance", "level" : "intermediate" } ], "majorSkills" : "Regulatory strategy, Compliance oversight, Risk management, Legal analysis", "majorSkillsList" : [ "Regulatory strategy", "Compliance oversight", "Risk management", "Legal analysis" ], "coreResponsibilities" : "Develop global regulatory strategies, Implement global regulatory strategies, Execute global regulatory strategies, Ensure compliance across product registration, Ensure compliance across lifecycle management, Ensure compliance across labeling, Ensure compliance across promotional material governance, Oversee regulatory workflows, Oversee regulatory tools, Manage global product lifecycle activities, Define global labeling requirements, Maintain global labeling requirements, Define regulatory procedures, Maintain regulatory procedures, Review marketing materials, Review advertising materials, Review promotional materials, Review training materials, Ensure compliance with regulatory requirements, Align global strategies, Share best practices, Drive cross-functional initiatives, Support regulatory readiness for audits, Support regulatory readiness for inspections, Support regulatory readiness for compliance assessments, Evaluate evolving global regulatory requirements, Translate regulatory requirements into guidance", "teamCollaboration" : "Partner closely with Business Unit; Partner with Commercial Regulatory Affairs; Work in matrixed environments; Work in global environments", "domainKnowledge" : "Global regulatory frameworks; In-vitro diagnostics; Regulated life sciences", "domainList" : [ "global-regulatory-frameworks", "in-vitro-diagnostics", "regulated-life-sciences" ], "domainSpecificKnowledge" : [ "Global regulatory frameworks", "In-vitro diagnostics", "Regulated life sciences" ], "toolProficiency" : [ "Microsoft Office tools", "Regulatory documentation systems" ], "communicationSkills" : "Written communication; Verbal communication; Translate complex topics", "documentationSkills" : "Regulatory documentation; Regulatory assessments", "continuousLearning" : "Professional development", "problemSolvingSkills" : "Critically assess applicability; Critically assess impact", "qualificationsBasic" : "Bachelor's degree in biological sciences, biomedical engineering, chemistry, or related field with 9+ years of relevant experience, Master's degree with 7+ years of relevant experience, PhD with 4+ years of relevant experience, Understanding of global regulatory frameworks, Experience in regulatory affairs, Ability to develop clear, structured regulatory documentation, Cross-functional collaboration skills, Excellent written and verbal communication skills, Proficiency in Microsoft Office tools, Proficiency in regulatory documentation systems", "qualificationsPreferred" : "Experience in in-vitro diagnostics, Experience in highly regulated life sciences industries", "remoteFriendly" : true, "workSiteFlexibility" : "Flexible", "rawDescription" : "## Accountabilities Develop, implement, and execute global regulatory strategies ensuring compliance across product registration, lifecycle management, labeling, and promotional material governance. Oversee regulatory workflows and tools used to manage global product lifecycle activities, ensuring efficiency, consistency, and compliance. Define and maintain global labeling requirements and regulatory procedures, ensuring alignment with international regulations and internal standards. Review and govern marketing, advertising, promotional, and training materials (MAPSS) to ensure compliance with applicable regulatory requirements. Partner closely with Business Unit and Commercial Regulatory Affairs teams to align global strategies, share best practices, and drive cross-functional initiatives. Support regulatory readiness for internal and external audits, inspections, and global compliance assessments. Evaluate evolving global regulatory requirements and translate them into actionable guidance for stakeholders across the organization. Requirements Bachelor’s degree in biological sciences, biomedical engineering, chemistry, or related field with 9+ years of relevant experience; or Master’s degree with 7+ years; or PhD with 4+ years. Strong understanding of global regulatory frameworks, with the ability to critically assess applicability and impact on products and processes. Experience in regulatory affairs, ideally within in-vitro diagnostics or other highly regulated life sciences industries. Ability to develop clear, structured regulatory documentation, assessments, and stakeholder-ready presentations. Strong cross-functional collaboration skills, with experience working in matrixed and global environments. Excellent written and verbal communication skills, with the ability to translate complex regulatory topics into actionable business guidance. Proficiency in Microsoft Office tools and regulatory documentation systems. Strong leadership, influence, and decision-making abilities, with the capacity to drive alignment across diverse teams. Benefits Annual salary range: $140,000 – $170,000, plus bonus and incentive eligibility. Comprehensive benefits package including medical, dental, vision, and retirement (401k) plans. Paid time off and programs supporting overall well-being and work-life balance. Flexible remote work arrangement with the option to work from home. Opportunity to shape global regulatory frameworks within a highly innovative diagnostics environment. Exposure to international regulatory strategy, product lifecycle governance, and cross-functional leadership. Inclusive, collaborative culture focused on continuous improvement and professional development. ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Staff Global Regulatory GPO. Skills: Regulatory strategy, Compliance oversight, Risk management, Legal analysis. Develop global regulatory strategies. Implement global regulatory strategies", "postedDate" : "2026-06-15T11:05:13.284", "createdAt" : "2026-06-15T11:05:13.284", "lastUpdated" : "2026-06-16T11:38:47.419", "ingestTimestamp" : "2026-06-16T03:23:23.041", "mongoId" : "6a30511af292fd229cefa721", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 140000, "salaryAnnualMax" : 170000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Product registration", "Global labeling requirements", "International regulations", "Internal standards", "Applicable regulatory requirements", "Global compliance", "Regulatory strategy", "Compliance oversight", "Risk management", "Legal analysis", "Lifecycle management", "Labeling governance", "Promotional material governance", "Regulatory workflows", "Regulatory procedures", "Marketing material review", "Advertising material review", "Promotional material review", "Training material review", "Regulatory readiness", "Compliance assessments", "Regulatory guidance development", "Stakeholder presentations", "Matrixed environments", "Global environments", "Leadership", "Influence", "Decision-making", "Global regulatory frameworks", "In-vitro diagnostics", "Regulated life sciences", "Microsoft Office tools", "Regulatory documentation systems" ], "skillCount" : 33, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Lead", "dataQualityScore" : 0.8888889, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "694ae6e370f0b99d589b3729", "title" : "Manager, External & Regulatory Affairs", "company" : "IAMGOLD", "industry" : "Government", "salary" : { "min" : 125000.0, "max" : 175000.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Manager in the Mining industry in Quebec City, Canada, adjusted for seniority and full-time employment." }, "location" : "33 - Quebec City Office", "locations" : [ "33 - Quebec City Office", "
33 - Quebec City Office (33 - Quebec City Office)
1020 rue Bouvier
suite 400
Quebec, G2K 0K9

" ], "timestamp" : "2026-06-15T06:46:06.990", "fingerprint" : "6518cf897e4e9534f3f7e8d764ede0e6a2f9a7246c6f2511719a86f3c8cf2507", "source" : "taleo", "language" : "en", "applyUrl" : "https://iamgold.taleo.net/careersection/ex/jobdetail.ftl?job=56981", "externalId" : "56981", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Quebec City", "state" : "Quebec", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "46.8137431,-71.2084061" }, { "country" : "Canada", "continent" : "na", "workMode" : "remote" } ], "locationText" : "Quebec City, Quebec, Canada; Canada", "minimumEducation" : "Bachelor's", "experienceMinYears" : 7, "experienceLevel" : "Manager", "professionalSkills" : [ "Public policy", "Regulatory outcomes", "Relationship building", "Strategic mindset" ], "hardSkillsList" : [ "Regulatory submissions", "Legislative analysis", "Risk analysis" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Regulatory submissions", "level" : "intermediate" }, { "name" : "Legislative analysis", "level" : "intermediate" }, { "name" : "Risk analysis", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "External affairs, Regulatory affairs, Stakeholder engagement", "majorSkillsList" : [ "External affairs", "Regulatory affairs", "Stakeholder engagement" ], "coreResponsibilities" : "Champion strategic priorities, Build relationships with government, Build relationships with Indigenous communities, Build relationships with key stakeholders, Support strategies influence public policy, Support strategies influence regulatory outcomes, Lead coordination project approval processes, Lead regulatory submissions, Lead communications government authorities, Serve as key liaison, Monitor legislative developments, Analyze legislative developments, Represent IAMGOLD industry associations, Guide senior leadership, Ensure alignment policy positions business objectives", "teamCollaboration" : "Internal teams; Government authorities; Indigenous communities; Key stakeholders; Industry associations", "projectManagementSkills" : [ "Project approval processes" ], "domainKnowledge" : "Quebec legislative regulatory landscape; Mining project approvals", "domainList" : [ "quebec-legislative-regulatory-landscape", "mining-project-approvals" ], "domainSpecificKnowledge" : [ "Quebec legislative regulatory landscape", "Mining project approvals" ], "communicationSkills" : "Stakeholder communications", "documentationSkills" : "Regulatory submissions", "problemSolvingSkills" : "Risk analysis", "specialRequirements" : "20-30% travel, Travel to Quebec sites, Travel to Toronto office", "qualificationsBasic" : "Bachelor's degree, 7 years relevant experience, Work on mining project approvals, Bilingualism French English, Understanding Quebec legislative regulatory landscape", "qualificationsPreferred" : "Experience in Quebec mining project approvals", "remoteFriendly" : true, "workSiteFlexibility" : "Flexible", "rawDescription" : "Empowering People – Extraordinary Performance Start Your Next Opportunity with IAMGOLD IAMGOLD is seeking a Manager, External & Regulatory Affairs to champion IAMGOLD’s strategic priorities in Quebec. This is a unique opportunity to shape the future of our projects by building strong relationships with government, Indigenous communities and other key stakeholders. In this role, you will be responsible for supporting and executing strategies that influence public policy and regulatory outcomes aligned with IAMGOLD’s operations and development projects in Quebec. You will lead the coordination of project approval processes, including regulatory submissions and communications with government authorities, and serve as a key liaison between IAMGOLD and external stakeholders. You will monitor and analyze legislative developments and represent IAMGOLD in industry associations. Your insights will guide senior leadership on political and regulatory risks and opportunities, while your collaboration with internal teams will ensure alignment between policy positions and business objectives. What You Need to Succeed To excel in this role, you’ll need a bachelor’s degree in political science, social sciences, sustainability, or a related field, along with a minimum of 7 years of relevant experience, ideally including work on mining project approvals in Quebec. Bilingualism in French and English is essential, as is a strong understanding of Quebec’s legislative and regulatory landscape. You’ll bring excellent communication and relationship-building skills, along with a strategic mindset and the ability to work independently and collaboratively. We offer an attractive total rewards package that includes a competitive salary and bonus, extended health, dental and insurance benefit coverage, a health spending account, fitness & wellness subsidy, employee & family assistance program, registered pension plan with company match, employee share purchase plan with company match, TFSA & RRSP, electric vehicle subsidy, summer hours and holiday office closure. This role is based in Quebec City with travel required (20–30%) to our sites in Quebec and our Corporate office in Toronto. We can consider remote candidates, depending on their location and travel flexibility. If you are a collaborative leader with a passion for public policy and engagement, we encourage you to apply. We understand no candidate meets every qualification listed. If your experience differs but you believe you can add value to the role, we want to hear from you! We are committed to inclusivity and welcome applications from individuals of all abilities. If you need accommodation during the application process, please contact us, and we'll provide the necessary support. Canada", "summaryDescription" : "Manager, External & Regulatory Affairs at IAMGOLD. Skills: External affairs, Regulatory affairs, Stakeholder engagement. Champion strategic priorities. Build relationships with government", "createdAt" : "2026-06-14T01:34:33.175", "lastUpdated" : "2026-06-15T06:46:06.990", "ingestTimestamp" : "2026-06-14T01:34:33.175", "mongoId" : "694ae6e370f0b99d589b3729", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "Regulatory submissions", "Legislative analysis", "Risk analysis", "Leadership", "External affairs", "Regulatory affairs", "Stakeholder engagement", "Public policy", "Regulatory outcomes", "Relationship building", "Strategic mindset", "Project approval processes", "Quebec legislative regulatory landscape", "Mining project approvals" ], "skillCount" : 14, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Manager", "dataQualityScore" : 0.7777778, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Mining", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c8cf574d8ee00a0977c5c", "title" : "Regulatory Affairs Pharmacovigilance Manager", "company" : "myTomorrows", "industry" : "Operations", "salary" : { "min" : 145000.0, "max" : 210000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Manager in the Healthcare industry in the US, adjusted for remote work and experience level." }, "location" : "US, Remote ", "locations" : [ "US, Remote ", "Canada ", "United Kingdom " ], "timestamp" : "2026-06-15T06:37:01.091", "fingerprint" : "de1fa88f12e49e886cbfb59c514138967dfdc82b54862fcd9d2bd0c4f6a8fa7d", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/mytomorrows/f90bd4cd-00ad-40da-bd95-80bca7efe655/application", "externalId" : "f90bd4cd-00ad-40da-bd95-80bca7efe655", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Manager", "professionalSkills" : [ "Regulatory strategy", "Risk management", "Legal analysis", "Compliance oversight" ], "hardSkillsList" : [ "Regulatory affairs", "Pharmacovigilance", "Regulatory dossier compilation", "Regulatory documentation", "SOP maintenance", "QI maintenance", "CAPA maintenance" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Regulatory affairs", "level" : "intermediate" }, { "name" : "Pharmacovigilance", "level" : "intermediate" }, { "name" : "Regulatory dossier compilation", "level" : "intermediate" }, { "name" : "Regulatory documentation", "level" : "intermediate" }, { "name" : "SOP maintenance", "level" : "intermediate" }, { "name" : "QI maintenance", "level" : "intermediate" }, { "name" : "CAPA maintenance", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "Regulatory affairs, Pharmacovigilance, Expanded Access Programs", "majorSkillsList" : [ "Regulatory affairs", "Pharmacovigilance", "Expanded Access Programs" ], "coreResponsibilities" : "Support regulatory strategies for EAPs, Act as Regulatory Affairs expert, Act as Pharmacovigilance expert, Communicate with clients, Submit to Health Authorities, Attend cross-functional meetings, Attend audits, Prepare regulatory dossiers, Compile regulatory dossiers, Submit regulatory dossiers, Provide input for regulatory strategy, Support new EAPs, Ensure compliant handling, Handle regulatory activities, Handle pharmacovigilance activities, Stay up to date on regulations, Assist in drafting documentation, Assist in reviewing documentation, Assist in maintaining documentation, Liaise with Pharmacovigilance provider, Contribute to maintaining SOPs, Contribute to maintaining QIs, Contribute to maintaining CAPAs", "teamCollaboration" : "Collaborate with Medical Affairs; Collaborate with Program Management; Collaborate with Quality Assurance; Collaborate with Supply Chain; Collaborate across teams; Work in cross-functional environment", "domainKnowledge" : "Expanded Access Programs; Biologicals; Cell therapies; Synthetic drugs; National legislation; International legislation", "domainList" : [ "expanded-access-programs", "biologicals", "cell-therapies", "synthetic-drugs", "national-legislation", "international-legislation" ], "domainSpecificKnowledge" : [ "Expanded Access Programs", "Biologicals", "Cell therapies", "Synthetic drugs", "National legislation", "International legislation" ], "toolProficiency" : [ "Microsoft 365", "Word", "Excel", "Teams", "SharePoint" ], "communicationSkills" : "Convey complex topics", "documentationSkills" : "Drafting regulatory documentation; Reviewing regulatory documentation; Maintaining regulatory documentation", "continuousLearning" : "Learning and development budget; Internal knowledge sharing", "problemSolvingSkills" : "Proactive problem solver; Identify regulatory challenges; Identify operational challenges; Suggest practical solutions", "specialRequirements" : "Reside within EST or CST", "qualificationsBasic" : "5 years relevant experience, Expanded Access experience, Working knowledge Pharmacovigilance, Bachelor's or Master's degree, Life Sciences degree, Experience with clients, Experience with external stakeholders", "qualificationsPreferred" : "Knowledge of additional languages", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "About myTomorrows myTomorrows is a global health tech company dedicated to breaking down barriers for patients seeking treatment options.    We strive to enable earlier and better treatment access by bridging the gap between those searching for possible options, and the companies who develop them. We work closely with patients, healthcare professionals, trial sites, patient advocacy groups, and BioPharma – connecting key stakeholders in the drug development ecosystem.    We’ve developed a cutting-edge AI-powered technology platform that simplifies and streamlines access to drugs in development. To support our users and clients, we have a range of industry-expert specialized teams ready to help. Our services include clinical trial patient recruitment, Expanded Access Program management and Real-World Data collection.    With a global footprint spanning 134 countries, to date we’ve supported over 17,000 patients, 3,000 physicians and 350 sites, earning the trust of 60+ BioPharma companies. In October 2025, we closed a €25M investment with Avego Healthcare Capital to fuel our global ambitions and scale the business.   Join us in shaping the future of treatment access - making tomorrow’s therapies accessible for people who need them today. The opportunity: Regulatory Affairs & Pharmacovigilance Manager As the Regulatory Affairs and Pharmacovigilance Manager, you will be responsible for ensuring compliance of our processes with country-specific expanded access regulations globally. In this role, you'll be a key contributor to our regulatory and quality infrastructure, keeping us aligned with global legislation. You will be actively working together with Medical Affairs, Program Management, Quality Assurance, and Supply Chain and will report to the Director of Regulatory Affairs and Pharmacovigilance (Emily says hi). Geographic Requirement: For candidates in North America, to ensure seamless collaboration with our teams, applicants must reside within the EST or CST time zones. What you will do in this role: - Support the development and execution of regulatory strategies for Expanded Access Programs (EAPs) involving biologicals, cell therapies, and synthetic drugs. - Act as the Regulatory Affairs and Pharmacovigilance expert for communications with clients (pharmaceutical companies) and submissions to Health Authorities, as well as cross-functional meetings and audits. - Prepare, compile, and submit regulatory dossiers for cohort and named patient Expanded Access Programs (EAPs) on behalf of clients. - Provide input and support for the regulatory strategy for setting up and executing EAPs (e.g., where, when, and how). - Collaborate with the Commercial team to support new EAPs. - Ensure timely and compliant handling of all regulatory and pharmacovigilance activities related to EAPs. - Stay up to date on relevant global laws, regulations, and guidelines impacting EAPs. - Assist in drafting, reviewing, and maintaining regulatory documentation and templates. - Liaise with the Pharmacovigilance service provider to ensure alignment and compliance. - Contribute to maintaining department documentation such as SOPs (Standard Operating Procedures), QIs (Quality Incidents), and CAPAs (Corrective and Preventive Actions). What you bring to the table: - Approximately 5 years of relevant experience in Regulatory Affairs, including experience in Expanded Access. - Working knowledge of fundamental principles of Pharmacovigilance is required. - Solid understanding of national and international legislation and regulation relating to Expanded Access - A Bachelor’s or Master's degree in Life Sciences or a related field - Experience working directly with clients or external stakeholders in a professional setting - Strong communication skills (written and verbal) in English; able to convey complex topics clearly to both internal teams and external parties. Knowledge of additional languages is a plus - Comfortable collaborating across teams and working in a cross-functional environment - Proactive problem solver with the ability to identify potential regulatory or operational challenges early and suggest practical solutions - Familiarity with Microsoft 365 tools (e.g., Word, Excel, Teams, SharePoint) What we offer: - Impactful work that helps patients gain access to potentially lifesaving treatments. - International work environment, scale-up energy and flat organizational structure which encourages creativity and accountability. - Competitive salary, annual performance bonus and an Employee Stock Option Plan. - Great career development opportunities in a fast-growing company. - Learning and development budget alongside internal knowledge sharing sessions. - Hybrid working model if you're in the Netherlands. - Policies to support working parents. - Healthy lunch at the thriving Amsterdam office. - Unlimited access to professional guidance by certified psychologists via OpenUp - Enjoy monthly events hosted by our vibrant Culture Club as well as an annual ‘myTomorrowland’ company-wide celebration! Equal opportunities myTomorrows is an Equal Opportunity Employer and, beyond upholding discrimination-free practices, we are committed to cultivating a workplace where difference and diversity are protected and celebrated. The best work comes from our best selves, and we go to great lengths in supporting our team members to be just that. ", "summaryDescription" : "Regulatory Affairs Pharmacovigilance Manager at myTomorrows. Skills: Regulatory affairs, Pharmacovigilance, Expanded Access Programs. Support regulatory strategies for EAPs. Act as Regulatory Affairs expert", "createdAt" : "2026-06-13T21:28:47.075", "lastUpdated" : "2026-06-15T06:37:01.091", "ingestTimestamp" : "2026-06-13T21:28:47.075", "mongoId" : "6a2c8cf574d8ee00a0977c5c", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 145000, "salaryAnnualMax" : 210000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Regulatory affairs", "Pharmacovigilance", "Regulatory dossier compilation", "Regulatory documentation", "SOP maintenance", "QI maintenance", "CAPA maintenance", "Leadership", "Expanded Access Programs", "Regulatory strategy", "Risk management", "Legal analysis", "Compliance oversight", "Biologicals", "Cell therapies", "Synthetic drugs", "National legislation", "International legislation", "Microsoft 365", "Word", "Excel", "Teams", "SharePoint" ], "skillCount" : 23, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Manager", "dataQualityScore" : 0.8888889, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2e9f7474d8ee00a0e3eb69", "title" : "Associate General Counsel, Regulatory Affairs", "company" : "Jackson", "industry" : "Legal", "salary" : { "min" : 225000.0, "max" : 350000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Associate General Counsel in the Insurance industry in Lansing, United States, adjusted for company size and seniority." }, "location" : "Lansing, MI", "locations" : [ "Lansing, MI", "United States of America" ], "timestamp" : "2026-06-16T04:58:46.162", "fingerprint" : "80fa88d3eaf68222115ffe1a42c596c75a6d65c0c1556653a4ebea6a68bfcc0c", "source" : "workday", "language" : "en", "applyUrl" : "https://jackson.wd1.myworkdayjobs.com/Jackson_Careers/job/Lansing-MI/Associate-General-Counsel--Regulatory-Affairs_REQ-03814", "externalId" : "REQ-03814", "industryFunction" : { }, "locationPoint" : "42.48424,-76.47994", "structuredLocations" : [ { "city" : "Lansing", "state" : "Michigan", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "42.7338254,-84.5546295" } ], "locationText" : "Lansing, Michigan, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Juris Doctor", "experienceMinYears" : 8, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "remoteFriendly" : false, "rawDescription" : "**_If you are an internal associate, please login to Workday and apply through Jobs Hub._** ## **_Job Purpose_** ## The Associate General Counsel, Regulatory Affairs provides advice to internal departments on a wide range of legal issues. The AGC coordinates regulatory interactions and examinations for Jackson's insurance and distribution businesses; oversees regulatory filings and other regulatory submissions; facilitates remediation of exam findings; provides leadership with regulatory examinations and interactions; assists with highly confidential projects; assists with the development and implementation of corporate policies; and coordinates legal and compliance efforts related to artificial intelligence, data governance, privacy, and social media. ## **_Essential Responsibilities_** ## * Coordinates responses to regulatory inquiries and examination requests, including matters received from state, federal, and international regulators. Partners and collaborates with key stakeholders across Jackson’s actuarial, finance, operations, insurance, and distribution businesses to identify key regulatory issues impacting the Company. * Responsible for preparation and timely submission of regulatory filings, amendments, and other confidential regulatory communications associated with Jackson’s domestic and international regulatory obligations. * Prepares interpretive guidance and coordinates regulatory implementations as requested. * Supports the Government Relations department with federal and state advocacy by providing technical expertise, including provision of model legislative and regulatory language and contributing to position papers on legislative and regulatory issues. * Reviews the Company’s policies for compliance with applicable laws and regulations and industry best practices and, where necessary, creates policies and procedures where none exist or updates existing policies. * Assists in the implementation and management of remediating items identified by regulators as either formal findings or potential issues arising from exams or identified internally by the Jackson Chief Compliance Officer. * Identifies trends within the regulatory landscape that may impact Jackson, especially those arising from exams, enforcement actions, and other state guidance. * Provides regular reporting on examination and regulatory activity both within Jackson and the marketplace at large. * Researches and handles legal issues, prepares legal and risk analysis as requested by the AVP, Regulatory Affairs; Jackson Chief Compliance Officer; and Enterprise Chief Compliance Officer. ## **_Other Duties_** ## * Occasional business travel may be required. * Performs other duties and/or projects as assigned. ## **_Knowledge, Skills and Abilities_** ## * Exceptional project management skills. * Excellent organizational and prioritization skills. * Strong attention to detail, editing, and proofreading skills. * Demonstrated ability to work independently and collaboratively in a team environment. * Exceptional ability to make decisions while operating in a fast-paced and deadline-oriented environment. * Excellent verbal, written, and presentation skills with the ability to articulate important legal concerns/principles to business units. * Excellent research, analysis, and drafting skills. * Exceptional critical thinking and analytical reasoning skills with the ability to provide alternate approaches and solutions. * Strong working knowledge of Microsoft Office, including Word, Access, Excel, and Outlook. * Effective at establishing and maintaining positive working relationships with management, colleagues, and internal and external contacts. * Possession of a strong business acumen. * Demonstrated mentoring skills. * Solid working knowledge of the life insurance and annuity industry, including operations and products. * Solid working knowledge of the broker-dealer and insurance agency industry, including operations, securities products, and sales processes. * Strong knowledge of state insurance and federal securities laws, regulations, and standards. * Familiarity with the use of Lexis to conduct legal research. ## **_Qualifications_** * ## Juris Doctor from ABA accredited law school required. * ## Member in good standing of a State Bar Association required. * ## 8+ years of prior legal experience required. * ## 8+ years of insurance and/or financial securities experience preferred. Jackson is proud to be an equal opportunity workplace. The Company subscribes to and endorses federal and state laws and regulations relating to equal employment opportunity for all persons without regard to race, color, religion, gender, age, national origin, legally-recognized disability, marital status, legally-protected medical condition, citizenship, ancestry, height, weight, sexual orientation, veteran status, or any other factor not related to the needs of the job. The Company is committed to a policy of equal opportunity. Company facilities and campuses are tobacco-free environments.", "summaryDescription" : "Associate General Counsel, Regulatory Affairs at Jackson", "postedDate" : "2026-06-12T21:26:49.309", "createdAt" : "2026-06-14T21:26:49.294", "lastUpdated" : "2026-06-16T04:58:46.162", "ingestTimestamp" : "2026-06-14T21:26:49.294", "mongoId" : "6a2e9f7474d8ee00a0e3eb69", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://jackson.wd1.myworkdayjobs.com/Jackson_Careers/job/Lansing-MI/Associate-General-Counsel--Regulatory-Affairs_REQ-03814", "salaryAnnualMin" : 225000, "salaryAnnualMax" : 350000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Insurance", "llmIndustryConfidence" : 0.98 }, { "id" : "6a305085f292fd229cef15ed", "title" : "Head of Policy and Regulatory Affairs – US", "company" : "Elliptic", "industry" : "Marketing", "salary" : { "min" : 155000.0, "max" : 290000.0, "currency" : "USD", "frequency" : "Yearly" }, "location" : "New York, United States", "locations" : [ "New York, United States", "Washington Office" ], "certifications" : [ "CAMS", "CFA", "FRM" ], "timestamp" : "2026-06-16T11:04:28.417", "fingerprint" : "763481b0e8af17ce68191c15a68a45fc67bb4d6f45788e43e1546aa53e9662df", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/elliptic/b8d9dab4-3af9-453d-bd87-29e1ab710e2b/application", "externalId" : "b8d9dab4-3af9-453d-bd87-29e1ab710e2b", "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" : 10, "experienceMaxYears" : 99, "experienceLevel" : "Executive", "professionalSkills" : [ "Public policy", "Regulatory engagement", "Government affairs", "Policy advocacy", "Thought leadership", "Client advisory", "Product development", "Client success", "Compliance strategy", "Risk mitigation", "Strategic relationships", "Industry analysis" ], "hardSkillsList" : [ "Regulatory analysis", "Policy analysis", "AML/CFT requirements", "Digital asset classification", "Blockchain analytics", "Crypto asset compliance" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Regulatory analysis", "level" : "intermediate" }, { "name" : "Policy analysis", "level" : "intermediate" }, { "name" : "AML/CFT requirements", "level" : "intermediate" }, { "name" : "Digital asset classification", "level" : "intermediate" }, { "name" : "Blockchain analytics", "level" : "intermediate" }, { "name" : "Crypto asset compliance", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "Digital Assets, Government Engagement, Financial Crime Prevention", "majorSkillsList" : [ "Digital Assets", "Government Engagement", "Financial Crime Prevention" ], "coreResponsibilities" : "Lead public policy engagement strategy, Lead regulatory engagement strategy, Engage with federal regulators, Engage with state regulators, Engage with policymakers, Engage with Congressional offices, Engage with international standard setters, Shape regulatory outcomes, Respond to policy frameworks, Respond to stablecoin legislation, Respond to AML/CFT requirements, Respond to digital asset classification, Strengthen regulatory voice, Strengthen thought leadership, Create authoritative content, Prepare Congressional testimony, Represent Elliptic externally, Advise internal teams, Empower internal teams, Provide regulatory insights, Provide regulatory analysis, Drive product development, Drive client success, Drive compliance strategy, Position Elliptic as partner, Serve as subject matter expert, Provide strategic advisory services, Build and maintain relationships, Represent Elliptic at conferences, Represent Elliptic at forums, Represent Elliptic at briefings, Represent Elliptic at meetings", "teamCollaboration" : "Global cross-functional team; Strategic Advisory team; Federal agencies; Congressional committees; State regulators; Industry associations; Financial institutions; Crypto native businesses; Government agencies; Financial authorities; Congressional staff; Policy communities", "domainKnowledge" : "Digital assets; Blockchain technology; Cryptocurrency; Financial crime prevention; Money laundering; Stablecoin legislation; FinCEN guidance; SEC jurisdiction; CFTC jurisdiction; State-level licensing; Federal frameworks; Key state regimes; NY BitLicense; State MTL frameworks; Digital asset economy", "domainList" : [ "digital-assets", "blockchain-technology", "cryptocurrency", "financial-crime-prevention", "money-laundering", "stablecoin-legislation", "fincen-guidance", "sec-jurisdiction", "cftc-jurisdiction", "state-level-licensing", "federal-frameworks", "key-state-regimes", "ny-bitlicense", "state-mtl-frameworks", "digital-asset-economy" ], "domainSpecificKnowledge" : [ "Digital assets", "Blockchain technology", "Cryptocurrency", "Financial crime prevention", "Money laundering", "Stablecoin legislation", "FinCEN guidance", "SEC jurisdiction", "CFTC jurisdiction", "State-level licensing", "Federal frameworks", "Key state regimes", "NY BitLicense", "State MTL frameworks", "Digital asset economy" ], "communicationSkills" : "Policy positions; Briefings; Public commentary; External representation; Executive meetings", "documentationSkills" : "Policy analysis; Regulatory updates; Congressional testimony preparation; Industry trend reports", "outcomesObjectives" : "Shape and respond to policy frameworks; Strengthen regulatory voice; Strengthen thought leadership; Drive product development; Drive client success; Drive compliance strategy; Position Elliptic as leading partner; Build trust in digital assets", "qualificationsBasic" : "5+ years experience in policy and regulatory affairs, Experience in US policy and regulatory engagement, Experience with federal and state regulators, Experience with Congressional offices, Experience with public sector stakeholders, Experience with crypto regulation, Experience with financial crime prevention, Experience with digital innovation, Experience with digital asset economy, Experience with FinCEN, Experience with SEC, Experience with CFTC, Experience with OCC, Experience with OFAC, Experience with state regulators, Experience with industry associations, Experience with blockchain technology, Experience with digital assets, Experience with regulatory compliance, Experience with government engagement, Experience with policy analysis, Experience with regulatory updates, Experience with industry trend reports, Experience with strategic relationships, Experience with federal agencies, Experience with Congressional committees, Experience with state-level regimes, Experience with NY BitLicense, Experience with state MTL frameworks, Experience working with federal agencies, Experience working with Congressional offices, Experience working with regulatory bodies, Experience working with intergovernmental institutions, Experience crafting policy positions, Experience crafting public commentary, Experience influencing regulatory outcomes, Experience with advocacy, Experience with collaborative engagement", "qualificationsPreferred" : "Former experience in federal regulatory body, Former experience in Congressional committee staff, Former experience in Treasury/FinCEN, Experience with stablecoins, Previous consulting experience, Previous advisory experience, Technical understanding of blockchain technology, Technical understanding of digital asset infrastructure, Experience developing training sessions, Experience delivering training sessions, Experience with international standard-setting bodies, Experience with FATF, Experience with Basel Committee", "remoteFriendly" : true, "workSiteFlexibility" : "Flexible", "rawDescription" : "At Elliptic, we believe cryptocurrency will play a huge role in the future of value transfer, and we care deeply about helping to build this future. In order for cryptocurrency to flourish, it’s important to prevent criminal abuse of the technology. Elliptic is the global leader in detecting, preventing, and pursuing criminal activity in cryptocurrencies. Our clients include the world’s leading cryptocurrency exchanges, financial institutions and government agencies. Our unique platform gives us an unparalleled understanding of cryptocurrency capital flows, using a combination of network science and machine learning to aggregate and interpret vast quantities of transaction data. We provide anti-money laundering (AML) compliance software and investigative services to the leading participants in the cryptocurrency ecosystem. Customers rely on us to analyse more than $150bn of their transactions every month, and include cryptocurrency businesses, major financial institutions, and federal government agencies. The company has a presence in London, UK, New York City, Singapore and Tokyo. We are backed by SBI Group, Albion VC, Octopus Ventures, SignalFire, Paladin Capital, Santander InnoVentures, and Digital Currency Group. Are you passionate, enthusiastic, and looking for an opportunity to grow your career in sales? Are you looking for your next challenge in an emerging and exciting market? If yes then we want to hear from you! The Impact You Will Have As Head of Policy and Regulatory Affairs – US, you will lead Elliptic’s public policy and regulatory engagement strategy across the United States, the most consequential jurisdiction shaping the future of digital assets. Based in Washington D.C. or New York, you will be Elliptic’s most senior voice on policy issues across the Americas, guiding our approach to engaging with federal and state regulators, policymakers, Congressional offices, and international standard setters. You will help shape regulatory outcomes across the evolving US landscape, including the Clarity Act, stablecoin frameworks, FinCEN guidance, SEC and CFTC jurisdiction, and state-level licensing regimes, while ensuring our strategy aligns with the rapidly evolving landscape of crypto regulation, financial crime prevention, and digital innovation. You will join a global, cross-functional team of regulatory specialists and subject matter experts, working at the forefront of engagement with governments, regulators, financial institutions, and crypto native businesses. In this commercially oriented role, you’ll act as a trusted advisor to existing and prospective clients, helping them navigate regulatory complexity, adopt Elliptic’s solutions with confidence, and meet their compliance objectives. Your policy insights will influence go-to-market strategies, support business development, and directly drive customer success, product-market fit, and revenue growth across the Americas. Your leadership will be instrumental in establishing Elliptic as the most trusted advisor for regulated institutions and public agencies seeking to understand and mitigate risks in the digital asset economy. Key Outcomes - Lead Elliptic’s strategic engagement with federal and state regulators, Congressional offices, and public sector stakeholders across the United States - Shape and respond to emerging crypto and digital asset policy frameworks, including stablecoin legislation, AML/CFT requirements, and digital asset classification - Strengthen Elliptic’s regulatory voice and thought leadership through policy advocacy, content creation, testimony preparation, and external representation - Advise and empower internal teams with regulatory insights and analysis to drive product development, client success, and compliance strategy - Position Elliptic as the leading technology partner for US government agencies and financial institutions building trust in digital assets What You Will Do - Serve as the primary subject matter expert on US policy, regulation, and government affairs related to digital assets and blockchain technology - Provide strategic advisory services to internal teams and external clients on regulatory compliance and government engagement - Develop thought leadership through authoritative content creation, including policy analysis, regulatory updates, Congressional testimony preparation, and industry trend reports - Work with our Strategic Advisory team to build and maintain strategic relationships with key stakeholders across federal agencies (FinCEN, SEC, CFTC, OCC, OFAC), Congressional committees, state regulators, and industry associations - Represent Elliptic at industry conferences, regulatory forums, Congressional briefings, and executive meetings with senior government and financial services leaders - Collaborate with product and engineering teams to provide expert guidance on regulatory requirements and institutional client needs - Advise on regulatory developments and market trends affecting digital asset policy and institutional adoption strategies - Support business development and enterprise sales processes with deep policy expertise and government relationship leverage - Contribute to cross-functional initiatives that accelerate responsible adoption of digital asset solutions within government and traditional finance - Build and maintain your professional profile through speaking engagements, media commentary, social media presence, and industry networking What You Will Achieve in the First 6 Months - Supported early customer engagements that demonstrate Elliptic’s regulatory expertise and strengthen confidence in our brand, and have been cited as a key expert resource by top prospects and customers - Delivered consistent, high-quality intelligence and policy insights to global stakeholders internally and externally - Established Elliptic as a credible and proactive voice in the US regulatory community - Work with our Strategic Advisory team to build upon our trusted relationships with at key regulators, Congressional offices, or (e.g., FinCEN, Treasury,) - Contributed visible US thought leadership content (publication, panel, consultation, or testimony) tied to Elliptic’s mission - Embedded the US as a critical contributor within the global Regulatory & Industry Affairs framework You Will Be a Great Fit Here If You - 10+ years of experience in regulatory affairs, public policy, government relations, or compliance, with a focus on financial services, digital assets, or public sector engagement - Deep understanding of the US digital asset regulatory landscape, including federal frameworks (SEC, CFTC, FinCEN, OCC, OFAC) and key state-level regimes (e.g., NY BitLicense, state MTL frameworks) - Experience working within or alongside federal agencies, Congressional offices, regulatory bodies, or intergovernmental institutions - Strong existing public-sector network across US financial authorities, Congressional staff, and policy communities - Exceptional communication skills, with experience crafting policy positions, briefings, and public commentary on complex legal and regulatory topics - Comfort working at the intersection of technology, law, and finance, including the regulatory applications of blockchain analytics and crypto asset compliance - Proven record of influencing regulatory outcomes through advocacy and collaborative engagement with policymakers and institutions - Passion for shaping the future of responsible crypto innovation, financial integrity, and regulatory clarity Bonus Points For - Former experience in a federal regulatory body, Congressional committee staff, or Treasury/FinCEN - Experience with stablecoins and their role in traditional finance and payments - Previous consulting or advisory experience in financial services or government affairs - Technical understanding of blockchain technology and digital asset infrastructure - Experience developing and delivering training and knowledge-sharing sessions - Experience working with international standard-setting bodies (FATF, Basel Committee) - Advanced degree in law, public policy, finance, economics, or related field - Professional qualifications in compliance or related fields (CAMS, CFA, FRM, etc.) - Experience in fintech, digital asset advisory, or crypto policy advocacy roles We know Diversity and Inclusion is much deeper than just hiring, but it is important for us to mention it here. We welcome and embrace individuals of all backgrounds and identities at Elliptic, and this is an ongoing priority for us.", "summaryDescription" : "Head of Policy and Regulatory Affairs – US at Elliptic. Skills: Digital Assets, Government Engagement, Financial Crime Prevention. Lead public policy engagement strategy. 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With offices in Minneapolis, MN, US; Geneva, Switzerland; and Brisbane and Perth, Australia, we have a growing and inclusive team. Our mission is to forge new frontiers in cardiac care by pioneering science-driven and measurable advancements to restore heart valve patients to healthy function. Transcatheter Aortic Valve Replacement (TAVR) technologies were originally designed for older, high-risk patients. Today, younger, more active patients need a better solution that will not just open and close but restore healthy heart function. We seek to restore healthy blood flow patterns by creating the world’s first biomimetic TAVR valve, DurAVR® THV. This cutting-edge valve, incorporating our proprietary ADAPT® anti-calcification technology, is designed to mimic the natural function of a healthy heart valve. Anteris Technologies is advancing innovative structural heart technologies designed to redefine expectations in the treatment of aortic stenosis. Our Clinical and Regulatory Affairs teams play a critical role in supporting clinical research, physician engagement, global regulatory strategy, and the advancement of breakthrough therapies through development and commercialization. We are interested in connecting with professionals with the following experience: Clinical operations Clinical monitoring Physician support Field clinical education Global regulatory compliance, or Clinical trial management within the medical device industry. Roles in Clinical & Regulatory Affairs include: Clinical Project Manager Clinical Research Associate Clinical Research Scientist Clinical Specialist Regulatory Affairs Specialist Candidates with experience supporting Class III medical devices, structural heart therapies, cardiovascular technologies, or global clinical studies are especially encouraged to apply. Successful candidates are collaborative, adaptable, organized, and comfortable operating within fast-paced, cross-functional environments. This is an opportunity to contribute directly to meaningful innovation while helping bring transformative therapies to patients worldwide. What We Offer: Opportunity to make a significant impact on the healthcare industry by advancing groundbreaking therapies. Collaborative and dynamic work environment with a culture of innovation and excellence. Competitive compensation package, including salary, performance-based bonuses, and stock options. Career development opportunities and a chance to be part of a growing company that values its employees. Health and Wellness Offerings: Medical, Dental, and Vision Plans Flexible Spending Account (FSA) 401k + Company Match Life, AD&D, Short Term and Long-Term Disability Insurance Bonus Plan Eligibility Employee Equity Program Paid Holidays & Vacation Employee Assistance Program Inclusive Team Environment These evergreen postings are designed to connect us with talented individuals interested in future opportunities at Anteris Technologies. Because openings may vary over time, additional details regarding specific responsibilities, qualifications, work arrangements, and compensation will be shared as candidates move forward in the process for individual roles. Note: We may require proof of COVID-19 vaccination to comply with health institutions, state, local municipality, and/or travel regulations. Anteris Technologies recruits, employs, trains, compensates, and promotes regardless of race, religion, color, national origin, sex, disability, age, veteran status, and other protected status as required by applicable law. We have a clear vision: to be a place of belonging for all humans by promoting diversity, multiculturism and inclusion, as a goal and reflection across the organization. Diversity is more than a commitment - it is part of our mission to deliver the best structural heart products on a global scale.", "summaryDescription" : "Clinical & Regulatory Affairs at Anteris Technologies", "postedDate" : "2026-06-12T22:07:07.379", "createdAt" : "2026-06-12T22:07:07.379", "lastUpdated" : "2026-06-15T00:31:00.279", "ingestTimestamp" : "2026-06-12T22:07:07.379", "mongoId" : "6a2c5eb374d8ee00a08e6055", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 95000, "salaryAnnualMax" : 135000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Structural heart", "Cardiac care", "Transcatheter Aortic Valve Replacement", "Medical device", "Global regulatory compliance", "Clinical trial management" ], "skillCount" : 6, "jobCategory" : "other", "jobSubcategory" : "clinical", "dataQualityScore" : 0.7777778, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "id" : "6a2c5e6674d8ee00a08e3c22", "title" : "Associate Director, Regulatory Affairs Medical Writing", "company" : "Beeline Medicines", "industry" : "Biotechnology", "salary" : { "min" : 175000.0, "max" : 250000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline data for Biotech industry in the United States, adjusted for Director seniority and company size." }, "location" : "United States", "locations" : [ "United States" ], "timestamp" : "2026-06-15T00:40:22.706", "fingerprint" : "bcde5195628fbada21a4539433c8bff772bc1b2ea6d12316189f4dc4623646c3", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/beelinemedicines/jobs/4235037009", "externalId" : "4235037009", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "hybrid" } ], "locationText" : "United States", "experienceLevel" : "Director", "professionalSkills" : [ "Regulatory affairs", "Scientific messaging", "Vendor management", "Submission strategy" ], "hardSkillsList" : [ "Medical writing", "Scientific accuracy", "Regulatory compliance", "ICH guidelines", "Pharmacovigilance documentation" ], "softSkillsList" : [ "Active listening" ], "hardSkills" : [ { "name" : "Medical writing", "level" : "intermediate" }, { "name" : "Scientific accuracy", "level" : "intermediate" }, { "name" : "Regulatory compliance", "level" : "intermediate" }, { "name" : "ICH guidelines", "level" : "intermediate" }, { "name" : "Pharmacovigilance documentation", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Active listening" } ], "majorSkills" : "Medical writing, Regulatory affairs, Scientific documentation", "majorSkillsList" : [ "Medical writing", "Regulatory affairs", "Scientific documentation" ], "coreResponsibilities" : "Own medical writing execution, Author regulatory documents, Coordinate scientific documents, Review scientific documents, Contribute to submission strategy, Lead scientific messaging consistency, Represent Medical Writing, Collaborate with Clinical Development, Collaborate with Nonclinical, Collaborate with Biostatistics, Collaborate with Safety, Collaborate with Regulatory Affairs, Provide guidance to contributors, Provide oversight to writers, Manage external writers, Own document timelines, Manage integrated trackers, Align on resourcing needs, Mitigate bottlenecks, Provide status updates, Establish authoring process, Establish review process, Establish QC process, Establish approval process, Develop training materials, Evaluate AI tools, Evaluate digital tools", "teamCollaboration" : "Cross-functional forums; Cross-functional review cycles; Cross-functional teams", "projectManagementSkills" : [ "Document timelines", "Deliverable tracking" ], "domainKnowledge" : "Immunology; Inflammation; Autoimmune disease; ICH CTD format; ICH E3; ICH E6; ICH E8; ICH M4; Pharmacovigilance documentation", "domainList" : [ "immunology", "inflammation", "autoimmune-disease", "ich-ctd-format", "ich-e3", "ich-e6", "ich-e8", "ich-m4", "pharmacovigilance-documentation" ], "domainSpecificKnowledge" : [ "Immunology", "Inflammation", "Autoimmune disease", "ICH CTD format", "ICH E3", "ICH E6", "ICH E8", "ICH M4", "Pharmacovigilance documentation" ], "toolProficiency" : [ "Veeva Vault" ], "communicationSkills" : "Scientific messaging; Verbal communication; Written communication; Executive presentations; Strategic updates", "documentationSkills" : "Regulatory documents; Scientific documents; Clinical documents; Nonclinical documents; Protocols; CSRs; IBs; SAPs; ICFs; INDs/CTAs; BLA/NDA components; CTD modules; Medical writing standards; SOPs; Templates; ICH requirements; Publication planning; Journal submissions; Congress submissions", "continuousLearning" : "Evolving regulatory guidance; Industry best practices", "innovationCreativity" : "AI tools; Digital tools", "problemSolvingSkills" : "Mitigate bottlenecks; Finding creative ways", "specialRequirements" : "Periodic travel to offices", "qualificationsBasic" : "Advanced degree in life sciences, 7+ years medical writing experience, Extensive experience authoring regulatory submissions, Thorough knowledge of FDA/EMA requirements, Experience developing Medical Writing SOPs, Proficiency with document management systems", "qualificationsPreferred" : "Deep scientific expertise in immunology, Experience building Medical Writing function, Publication planning experience", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "About Beeline Medicines: Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully. Job Summary: The Associate Director, Regulatory Affairs Medical Writing is a hands-on role responsible for clear scientific messaging, the development and coordination of high-quality regulatory, nonclinical, clinical, and other scientific documents in support of the company’s I the incumbent will be expected to travel to Beeline Medicines’ offices on a periodic basis to support in-person collaboration, team engagement, and business operations. The frequency and scheduling of such visits will be determined at the company's discretion based on business need. Essential Duties and Responsibilities: Own day‑to‑day execution of medical writing activities, contributing directly to authoring and quality review while coordinating internal and external resources to ensure high‑quality, on‑time delivery of regulatory and scientific documents. Author, coordinate, and review key clinical and regulatory documents, including protocols and amendments, CSRs, IBs, SAPs, ICFs, INDs/CTAs, and selected BLA/NDA components, ensuring scientific accuracy, regulatory compliance, and consistency of content. Contribute to shaping the strategy for submission narratives and key messages, leading scientific messaging consistency across CTD modules. Represent Medical Writing in relevant cross‑functional and governance forums to support alignment on submission strategy and document readiness. Collaborate closely with Clinical Development, Nonclinical, Biostatistics, Safety, and Regulatory Affairs to plan, sequence, and execute document deliverables, coordinating cross‑functional review cycles and ensuring timely, integrated input. Provide practical guidance and oversight to internal contributors and external medical writers, including vendor management, scope definition, deliverable tracking, and consistent application of Medical Writing standards, templates, and SOPs aligned with ICH and regional requirements. Own document timelines and individually or in collaboration with project management, maintain and actively manage integrated trackers across programs, partnering with line management to align on resourcing needs, anticipate and mitigate bottlenecks, and finding creative ways to provide regular, transparent status updates to cross‑functional teams and leadership. Establish a clear process for the authoring, review, QC and approval of regulatory documents to be submitted to heath authorities. Develop training materials for the cross functional team to ensure adoption of the agreed process. Collaborate with IT, Quality, and Regulatory stakeholders to evaluate AI and digital tools that enhance medical writing efficiency and consistency, while ensuring compliance with data privacy, system validation, and regulatory expectations; remain current on evolving regulatory guidance and industry best practices. Perform other duties and responsibilities as assigned. Qualifications: Education: Advanced degree (PhD, PharmD, or master's level) in life sciences, pharmacology, biomedical sciences, or a related discipline required. Minimum of 7+ years of medical writing experience in the pharmaceutical or biotech industry, Extensive experience authoring and overseeing regulatory submissions in ICH CTD format, including CSRs, ISS/ISE, IBs, and IND/CTA packages. Deep scientific expertise in immunology, inflammation, or autoimmune disease is strongly preferred, with the ability to rapidly acquire technical knowledge in new therapeutic areas. Demonstrated ability to manage multiple concurrent document deliverables and writing teams in a high-priority regulatory environment. Thorough knowledge of FDA and EMA regulatory writing requirements, ICH E3, E6, E8, and M4 guidelines, and applicable pharmacovigilance documentation standards. Experience developing and enforcing Medical Writing SOPs, style guides, and document templates in a regulated pharmaceutical environment. Proficiency with document management systems, electronic submission tools, and publishing platforms such as Veeva Vault or equivalent. Strong publication planning experience, including familiarity with ICMJE authorship guidelines, journal submission processes, and scientific congress submission requirements. Experience building or scaling a Medical Writing function in an early-stage or rapidly growing biotech organization is highly desirable. Exceptional written and verbal communication skills with demonstrated ability to translate complex scientific, regulatory, or operational content for diverse audiences, including executive leadership, clinical teams, and external partners. Skilled at preparing and delivering compelling presentations, briefing documents, and strategic updates to cross-functional leadership teams and board-level stakeholders. Strong active listening skills and the ability to synthesize input from diverse perspectives into clear, actionable communications that build alignment and drive decision-making. Salary Range: The expected annual salary range for this position is listed below. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance. Salary Range $193,000—$215,000 USD Benefits: We offer a comprehensive benefits package including: Medical, Dental & Vision insurance (employee premiums 100% covered by company) 20 accrued days combined time off (PTO/Sick), 12 company holidays, & winter recharge Flexible work arrangements / hybrid schedule Health Savings Account (HSA) *Benefits are subject to eligibility requirements and plan terms. Additional details provided during the offer process* Equal Employment Opportunity: Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law. Reasonable Accommodation: If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates. Privacy Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at Privacy Policy - Beeline Medicines", "summaryDescription" : "Associate Director, Regulatory Affairs Medical Writing at Beeline Medicines. Skills: Medical writing, Regulatory affairs, Scientific documentation. Own medical writing execution. Author regulatory documents", "postedDate" : "2026-06-12T22:09:09.187", "createdAt" : "2026-06-12T22:09:09.187", "lastUpdated" : "2026-06-15T00:40:22.706", "ingestTimestamp" : "2026-06-12T22:09:09.187", "mongoId" : "6a2c5e6674d8ee00a08e3c22", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 175000, "salaryAnnualMax" : 250000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Medical writing", "Scientific accuracy", "Regulatory compliance", "ICH guidelines", "Pharmacovigilance documentation", "Active listening", "Regulatory affairs", "Scientific documentation", "Scientific messaging", "Vendor management", "Submission strategy", "Document timelines", "Deliverable tracking", "Immunology", "Inflammation", "Autoimmune disease", "ICH CTD format", "ICH E3", "ICH E6", "ICH E8", "ICH M4", "Veeva Vault" ], "skillCount" : 22, "jobCategory" : "other", "jobSubcategory" : "regulatory-&-quality", "dataQualityScore" : 0.8888889, "daysOld" : 2, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotechnology" }, { "id" : "69dde45b2beec4dd3d9a3ec4", "title" : "Manager, Transfusion Medicine - Quality & Regulatory Affairs", "company" : "City of Hope", "salary" : { "min" : 155000.0, "max" : 220000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Manager in Healthcare in Duarte, CA, adjusted for seniority and company size." }, "location" : "United States-California-Duarte", "locations" : [ "United States-California-Duarte", "Transfusion Medicine", "Hybrid, Days, Days" ], "timestamp" : "2026-06-15T23:52:29.836", "fingerprint" : "429c8ee2965af0a2b3bfce6e453eb8a0dbdf931bd13ecdc0574544477275a4e4", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=207464", "externalId" : "207464", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Duarte", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "34.1394513,-117.9772873" } ], "locationText" : "Duarte, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 5, "experienceLevel" : "Manager", "remoteFriendly" : false, "rawDescription" : "Manager, Quality & Regulatory Affairs Join the transformative team at City of Hope , where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. The Division of Transfusion Medicine is seeking a dynamic and experienced Manager to lead key initiatives in quality assurance, regulatory compliance, and information systems integration. This pivotal role ensures operational excellence across all areas of the division, while maintaining alignment with institutional values and strategic goals. As a successful candidate, you will: Lead and manage staff responsible for quality, compliance, and regulatory affairs Oversee the integration and compliance of Transfusion Medicine information systems and data across the division Ensure adherence to regulatory standards and maintain licensing/accreditation through direct interaction with external agencies Collaborate with the Director of Transfusion Medicine to implement strategic initiatives that support the division’s mission and vision Drive continuous improvement in operational workflows and data integrity Your qualifications should include: Bachelor of Science degree 5+ years of experience in Blood Banking and blood/cell therapy manufacturing (or equivalent regulated medical manufacturing environment) with 3 years of supervisory experience.    California license as a Clinical Laboratory Scientist or Immunohematology limited license; or will obtain either California license within 6 months from date of hire. City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . United States-California-Duarte", "summaryDescription" : "Manager, Transfusion Medicine - Quality & Regulatory Affairs at City of Hope", "createdAt" : "2026-06-14T18:54:32.989", "lastUpdated" : "2026-06-15T23:52:29.836", "ingestTimestamp" : "2026-06-14T18:54:32.989", "mongoId" : "69dde45b2beec4dd3d9a3ec4", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 155000, "salaryAnnualMax" : 220000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Manager", "dataQualityScore" : 0.7777778, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c7b5d74d8ee00a094954b", "title" : "Senior International Regulatory Affairs Specialist", "company" : "Butterfly Network", "industry" : "Healthcare", "salary" : { "min" : 110000.0, "max" : 115000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Burlington, Massachusetts, United States", "locations" : [ "Burlington", "Massachusetts", "United States", "New York", "New York", "United States" ], "timestamp" : "2026-06-15T07:45:52.304", "fingerprint" : "08e1e8f61dbbb6d7fe22168299ba7f62f6d7c6e94f6f78f99e3176a1799da48f", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://www.butterflynetwork.com/careers?gh_jid=7733539003", "externalId" : "7733539003", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Burlington", "state" : "Massachusetts", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "42.5048167,-71.1956111" } ], "locationText" : "Burlington, Massachusetts, United States", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Regulatory strategy", "Market access", "Risk management", "Compliance oversight", "Legal analysis" ], "hardSkillsList" : [ "Regulatory affairs", "Medical device submissions", "Product change assessment", "Global regulatory pathways", "Post-market surveillance", "Audit readiness" ], "hardSkills" : [ { "name" : "Regulatory affairs", "level" : "intermediate" }, { "name" : "Medical device submissions", "level" : "intermediate" }, { "name" : "Product change assessment", "level" : "intermediate" }, { "name" : "Global regulatory pathways", "level" : "intermediate" }, { "name" : "Post-market surveillance", "level" : "intermediate" }, { "name" : "Audit readiness", "level" : "intermediate" } ], "majorSkills" : "International regulatory affairs, Medical device regulations, Global market access, Regulatory submissions", "majorSkillsList" : [ "International regulatory affairs", "Medical device regulations", "Global market access", "Regulatory submissions" ], "coreResponsibilities" : "Support global regulatory strategies, Support Class II devices, Support Software in Medical Device, Coordinate international regulatory submissions, Prepare regulatory submission documentation, Integrate cross-functional inputs, Support timelines and deliverables, Maintain product registrations, Maintain renewals, Maintain amendments, Ensure compliance, Partner with cross-functional teams, Escalate issues, Escalate resource needs, Support post-market regulatory activities, Support renewals, Support variations, Support compliance maintenance, Maintain awareness of global regulations, Support audit readiness", "teamCollaboration" : "Cross-functional teams; Product development teams; Software development teams; Quality Assurance; Engineering", "domainKnowledge" : "Medical devices; Software in Medical Device; EU MDR 2017/745; MDSAP; APAC; MEA; LATAM; ISO 13485; ISO 14971; IEC 62304; Quality Management System", "domainList" : [ "medical-devices", "software-in-medical-device", "eu-mdr-2017-745", "mdsap", "apac", "mea", "latam", "iso-13485", "iso-14971", "iec-62304", "quality-management-system" ], "domainSpecificKnowledge" : [ "Medical devices", "Software in Medical Device", "EU MDR 2017/745", "MDSAP", "APAC", "MEA", "LATAM", "ISO 13485", "ISO 14971", "IEC 62304", "Quality Management System" ], "documentationSkills" : "Regulatory submission documentation", "problemSolvingSkills" : "Risk identification; Solution identification", "outcomesObjectives" : "Enable global market access; Drive high-quality submissions; Keep programs on track", "qualificationsBasic" : "Bachelor's degree, 5+ years regulatory affairs, Class II or higher devices, Software-enabled medical devices, Software in Medical Device, Software as Medical Device, International regulatory submissions, MDSAP countries, APAC, MEA, LATAM, EU MDR 2017/745, ISO 13485, ISO 14971, IEC 62304, Quality Management System, Change control, Design control, Lifecycle management", "qualificationsPreferred" : "Advanced degree preferred", "workSiteFlexibility" : "Hybrid", "rawDescription" : "Senior International Regulatory Affairs Specialist Company Description Butterfly Network, Inc. (NYSE: BFLY) is driving a digital revolution in ultrasound imaging and sensing with its proprietary Ultrasound-on-Chip™ semiconductor technology and software solutions. Butterfly first proved its technology in the point-of-care ultrasound market – commercializing the world’s first single-probe, whole-body portable ultrasound device, which is now on its best-selling, third-generation: Butterfly iQ3™. The Company combines its advanced hardware with cloud software and AI, an enterprise workflow solution (Compass AI™) and other offerings to drive adoption of affordable, accessible ultrasound. Butterfly also enables third-party development of imaging AI apps through Butterfly Garden™, its software development kit and AI partnership initiative. In addition to its medical imaging products, Butterfly Embedded™ is the Company’s Ultrasound-on-Chip™ licensing and co-development program designed to enable a new wave of ultrasound-enabled technologies across non-competitive healthcare markets and beyond. Through Butterfly Embedded™, partners can build and scale novel ultrasound applications powered by Butterfly’s proprietary semiconductor chip and software platform. Butterfly’s innovations have been recognized by Prix Galien USA, Fierce 50, TIME’s Best Inventions and Fast Company’s World Changing Ideas, among other achievements. We’re a team of bold thinkers, problem-solvers, and innovators ready to shape the future of medical imaging. Let’s build something extraordinary together! Job Description As a Senior Specialist, International Regulatory Affairs at Butterfly Network, you will play a key role in enabling global market access for innovative, hardware and software medical devices. You will support the execution of regulatory strategies and drive high-quality submissions across complex international markets, including APAC, MEA, LATAM, and MDSAP-participating countries. This role requires a strong ability to translate evolving regulatory requirements—such as EU MDR 2017/745—into clear, actionable plans, while partnering cross-functionally to align regulatory expectations with fast-paced product and software development cycles. You will assess the impact of product and software changes, navigate global regulatory pathways, and proactively identify risks and solutions to keep programs on track. Success in this role requires a highly organized, analytical, and self-driven regulatory professional who is comfortable operating in a dynamic environment, managing competing priorities, and contributing to the advancement of cutting-edge healthcare technologies on a global scale. As part of our team, your core responsibilities will be: Support execution of global regulatory strategies for Class II and higher medical devices, including Software in a Medical Device (SiMD) Contribute to and coordinate international regulatory submissions and registrations across APAC, MEA, LATAM, and MDSAP-participating countries Prepare and manage regulatory submission documentation, integrating cross-functional inputs and supporting timelines and deliverables Maintain product registrations, renewals, and amendments in accordance with country-specific requirements to support global market access Ensure compliance with global regulatory frameworks, including EU MDR 2017/745 and other applicable standards and regulations Partner with cross-functional teams (R escalate issues and resource needs as appropriate Support post-market regulatory activities, including renewals, variations, and compliance maintenance while maintaining awareness of evolving global regulations and supporting audit readiness within a QMS-driven environment Qualifications Baseline skills/experiences/attributes: Bachelor’s degree in a scientific, engineering, or related discipline (advanced degree preferred) At least 5+ years of progressive regulatory affairs experience in the medical device industry, including Class II or higher devices Demonstrated experience with software-enabled medical devices, including Software in a Medical Device (SiMD) and Software as a Medical Device (SaMD) Proven track record of supporting international regulatory submissions and market expansion, with hands-on experience across multiple regions, including: MDSAP countries, APAC, MEA and LATAM Strong working knowledge of global regulatory frameworks, including EU MDR 2017/745, and solid familiarity with international standards such as ISO 13485, ISO 14971, and IEC 62304 Experience operating within a Quality Management System (QMS), with exposure to structured regulatory processes such as change control, design control, and lifecycle management Ability to manage multiple projects and competing priorities in a fast-paced environment Strong verbal and written communication and presentation skills, with the ability to communicate clearly and effectively in English Demonstrated ability to ethical judgment within regulatory frameworks and company policies Collaborative team player with a service-oriented mindset; flexible and proactive in adapting to changing business needs Independent thinker with the ability to identify problems and develop creative, compliant solutions. Ideally, you also have these skills/experiences/attributes (but it’s ok if you don’t!): Experience in Artificial Intelligence/Machine Learning (AI/ML) Regulatory Affairs Certification (RAC). Values Innovation is what we do. Our values are how we make it happen. Butterflies are and believe in… Patient-Centric Innovators: Our mission is THE mission. Empowered to Impact: Every voice matters. One Team, One Goal: Unity fuels progress. Growth Champions: We embrace challenges. Action-Oriented Achievers: We follow through, every time. Location Butterfly offers a hybrid work model for most positions, with team members spending two or more days a week in the office. While flexibility is key, we value in-person connections that spark creativity and teamwork. Our offices are designed for collaboration, with comfortable workspaces, stocked kitchens, and opportunities to connect with peers. This is a hybrid position that can be based in Burlington, MA or New York City, NY Benefits and Perks Comprehensive health insurance, encompassing dental and vision coverage, is provided to all our employees. As a health-tech company, we prioritize the well-being of our teams. Additionally, employees have the option to buy up for enhanced health insurance coverage. We also contribute to Health Savings Account (HSA) accounts for all enrolled employees on an annual basis. Comprehensive Employee Assistance Program - we provide access to tools and resources to support your emotional health and day-to-day needs. 401k plan and match - we facilitate your retirement goals. Eligible employees will have the opportunity to participate in Employee Stock Purchase Plan (ESPP) Unlimited Paid Time Off + 10 Holiday Days a Year - recharge and come back ready to make an impact Parental Leave - we aim to provide our employees with time to bond with their growing family, along with additional support for primary caregivers to help transition back to work Competitive salaried compensation - we value our employees and show it Equity - we want every employee to be a stakeholder The opportunity to build a revolutionary healthcare product and save millions of lives! Compensation Our estimated salary for this role is $110,000 - $115,000 + bonus + equity + benefits. Actual pay is determined by multiple factors such as skills, qualifications, experience and market demand. For this role, we are only considering candidates who are legally authorized to work in the United States and who do not now or in the future require sponsorship for employment visa status. Butterfly Network does not accept agency resumes. Butterfly Network is an E-Verify Company. Butterfly Network is an equal opportunity employer. Regardless of race, traits associated with race, color, ancestry, religion, gender, national origin, sexual orientation, age, citizenship, marital status, disability or Veteran status. All your information will be kept confidential according to EEO guidelines. Butterfly requires security adherence responsibilities from all employees. These include: adhering to all company security policies and procedures, utilize provided company assets securely, and complete all required security awareness training programs. Safeguarding company data and systems from unauthorized access, modification, or destruction, contributing to the overall security posture of the organization. Immediately reporting any suspected or actual security incidents, including phishing attempts, malware infections, or unauthorized access, following the established incident response procedures. #LI-KG #KG-LI", "summaryDescription" : "Senior International Regulatory Affairs Specialist at Butterfly Network. Skills: International regulatory affairs, Medical device regulations, Global market access, Regulatory submissions. Support global regulatory strategies. Support Class II devices", "postedDate" : "2026-06-13T21:03:59.367", "createdAt" : "2026-06-13T21:03:59.367", "lastUpdated" : "2026-06-15T07:45:52.304", "ingestTimestamp" : "2026-06-13T21:03:59.367", "mongoId" : "6a2c7b5d74d8ee00a094954b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 110000, "salaryAnnualMax" : 115000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Regulatory affairs", "Medical device submissions", "Product change assessment", "Global regulatory pathways", "Post-market surveillance", "Audit readiness", "International regulatory affairs", "Medical device regulations", "Global market access", "Regulatory submissions", "Regulatory strategy", "Market access", "Risk management", "Compliance oversight", "Legal analysis", "Medical devices", "Software in Medical Device", "EU MDR 2017/745", "MDSAP", "APAC", "MEA", "LATAM", "ISO 13485", "ISO 14971", "IEC 62304", "Quality Management System" ], "skillCount" : 26, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Senior", "dataQualityScore" : 0.8888889, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a307110f292fd229cff7b12", "title" : "Staff Digital Design Engineer", "company" : "Renesas Electronics", "industry" : "Semiconductors", "salary" : { "min" : 2200000.0, "max" : 3500000.0, "currency" : "TWD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Lead Staff Digital Design Engineer in Zhubei, Taiwan, adjusted for the technology industry and company size." }, "location" : "Zhubei, TW", "locations" : [ "Zhubei", "TW" ], "timestamp" : "2026-06-16T10:03:37.490", "fingerprint" : "a329024bc84146e5337520b74503df098ca71391a9e5076b9400dadd29fe3612", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/RenesasElectronics/744000132165629-staff-digital-design-engineer", "externalId" : "744000132165629", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Zhubei", "country" : "Taiwan", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "24.8396820,121.0040779" } ], "locationText" : "Zhubei, Taiwan", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "remoteFriendly" : false, "rawDescription" : "Renesas is one of the top global semiconductor companies in the world. We strive to develop a safer, healthier, greener, and smarter world, and our goal is to make every endpoint intelligent by offering product solutions in the automotive, industrial, infrastructure and IoT markets. Our robust product portfolio includes world-leading MCUs, SoCs, analog and power products, plus Winning Combination solutions that curate these complementary products. We are a key supplier to the world’s leading manufacturers of electronics you rely on every day; you may not see our products, but they are all around you. Renesas employs roughly 21,000 people in more than 30 countries worldwide. As a global team, our employees actively embody the Renesas Culture, our guiding principles based on five key elements: Transparent, Agile, Global, Innovative, and Entrepreneurial. Renesas believes in, and has a commitment to, diversity and inclusion, with initiatives and a leadership team dedicated to its resources and values. At Renesas, we want to build a sustainable future where technology helps make our lives easier. Join us and build your future by being part of what’s next in electronics and the world. * Design optimized digital blocks meeting functional, cost and low power constraints and ensure spec compliance. * Cover digital backend design from synthesis, upf, static timing analysis and logic equivalent checking. * Interface with P&R for digital hand-off and post layout verification. * Collaboration with analog engineers and test engineers on analog testability design and debugging. * Work closely with Application/GUI team in FPGA prototype and lab debugging. * Perform physical silicon device evaluation where necessary. ## Qualifications * 7+ years of experience in ASIC/IC design with deep knowledge of whole IC design flow from RTL coding, synthesis, static timing analysis, logic equivalent checking to post-layout checking. * Experience in DFT or physical design is a plus. * Experience in FPGA prototype and lab equipment and lab debug is a plus. * Fluent in either Verilog RTL coding and ASIC design methodology. * Competence in developing design constraints for synthesis, STA and P&R handoff. * Ability to work both independently and part of a team. * Excellent interpersonal, organizational and communications skills. ## Additional Information Renesas is an embedded semiconductor solution provider driven by its Purpose ‘To Make Our Lives Easier.’ As the industry’s leading expert in embedded processing with unmatched quality and system-level know-how, we have evolved to provide scalable and comprehensive semiconductor solutions for automotive, industrial, infrastructure, and IoT industries based on the broadest product portfolio, including High Performance Computing, Embedded Processing, Analog & Connectivity, and Power. With a diverse team of over 21,000 professionals in more than 30 countries, we continue to expand our boundaries to offer enhanced user experiences through digitalization and usher into a new era of innovation. We design and develop sustainable, power-efficient solutions today that help people and communities thrive tomorrow, ‘To Make Our Lives Easier.’ At Renesas, you can: * Launch and advance your career in technical and business roles across four Product Groups and various corporate functions. You will have the opportunities to explore our hardware and software capabilities and try new things. * Make a real impact by developing innovative products and solutions to meet our global customers' evolving needs and help make people’s lives easier, safe and secure. * Maximize your performance and wellbeing in our flexible and inclusive work environment. Our people-first culture and global support system, including the remote work option and Employee Resource Groups, will help you excel from the first day. Are you ready to own your success and make your mark? Join Renesas. Let’s Shape the Future together. Renesas Electronics is an equal opportunity and affirmative action employer, committed to supporting diversity and fostering a work environment free of discrimination on the basis of sex, race, religion, national origin, gender, gender identity, gender expression, age, sexual orientation, disabilities, military status, veteran status, or any other basis protected by law. For more information, please read our [Diversity & Inclusion Statement](https://jobs.renesas.com/diversity-and-inclusion).", "summaryDescription" : "Staff Digital Design Engineer at Renesas Electronics", "postedDate" : "2026-06-15T10:28:27.000", "createdAt" : "2026-06-16T01:31:31.297", "lastUpdated" : "2026-06-16T10:03:37.490", "ingestTimestamp" : "2026-06-16T01:31:31.297", "mongoId" : "6a307110f292fd229cff7b12", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Lead", "dataQualityScore" : 0.8888889, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2b975674d8ee00a0816d18", "title" : "Regulatory Affairs Specialist", "company" : "Medtronic", "industry" : "Healthcare", "salary" : { "min" : 7500000.0, "max" : 1.2E7, "currency" : "ARS", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Regulatory Affairs Specialist in Buenos Aires, Argentina, adjusted for the Healthcare industry and Medtronic's company size." }, "location" : "Buenos Aires, Ciudad Autónoma de Buenos Aires, Argentina", "locations" : [ "Buenos Aires, Ciudad Autónoma de Buenos Aires, Argentina" ], "certifications" : [ "GMP", "GDP", "ISO 13485" ], "timestamp" : "2026-06-14T22:21:27.909", "fingerprint" : "76ff153ab5d77b0f93cca2d8520451080a8edaf4ec33ef32319db898e6274064", "source" : "workday", "language" : "es", "applyUrl" : "https://medtronic.wd1.myworkdayjobs.com/RedeploymentMedtronicCareers/job/Buenos-Aires-Ciudad-Autnoma-de-Buenos-Aires-Argentina/Regulatory-Affairs-Specialist--Argentina_R67027", "externalId" : "R67027", "industryFunction" : { }, "locationPoint" : "-5.2671,-79.96759", "structuredLocations" : [ { "city" : "Buenos Aires", "state" : "Ciudad Autónoma de Buenos Aires", "country" : "Argentina", "continent" : "sa", "source" : "llm", "workMode" : "hybrid", "geo" : "-34.6095579,-58.3887904" } ], "locationText" : "Buenos Aires, Ciudad Autónoma de Buenos Aires, Argentina", "employmentType" : "FULL_TIME", "experienceMinYears" : 2, "experienceMaxYears" : 3, "professionalSkills" : [ "Regulatory affairs", "Documentation preparation", "Regulatory submissions", "License renewal", "Annual registrations", "Labeling changes", "Manufacturing changes", "Marketing changes", "Clinical protocols", "Regulatory compliance", "Tracking systems", "Control systems", "Regulatory procedures", "Regulatory changes", "Agency interaction", "Clinical trial applications" ], "hardSkillsList" : [ "Regulatory filing", "Validation", "Modification", "Registration", "Audit", "CAPA" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Regulatory filing", "level" : "intermediate" }, { "name" : "Validation", "level" : "intermediate" }, { "name" : "Modification", "level" : "intermediate" }, { "name" : "Registration", "level" : "intermediate" }, { "name" : "Audit", "level" : "intermediate" }, { "name" : "CAPA", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "Regulatory Affairs, Medical Devices, Argentina Regulations", "majorSkillsList" : [ "Regulatory Affairs", "Medical Devices", "Argentina Regulations" ], "coreResponsibilities" : "Coordinate and prepare documentation for regulatory submissions, Prepare documentation for internal audits and inspections, Compile materials for submissions, Compile materials for license renewal, Compile materials for annual registrations, Recommend changes to labeling, Recommend changes to manufacturing, Recommend changes to marketing, Recommend changes to clinical protocols, Ensure regulatory compliance, Improve tracking systems, Improve control systems, Stay up-to-date on regulatory procedures, Stay up-to-date on regulatory changes, Interact with regulatory agencies, Recommend strategies for clinical trial approval", "teamCollaboration" : "Cross-functional teams", "domainKnowledge" : "Medical devices; Argentinian regulations; COFEPRIS; ANMAT; DIGEMID; Good Practices; ISO 13485", "domainList" : [ "medical-devices", "argentinian-regulations", "cofepris", "anmat", "digemid", "good-practices", "iso-13485" ], "domainSpecificKnowledge" : [ "Medical devices", "Argentinian regulations", "COFEPRIS", "ANMAT", "DIGEMID", "Good Practices", "ISO 13485" ], "documentationSkills" : "Regulatory filings", "continuousLearning" : "Mentoring; Networking", "qualificationsBasic" : "Carrera universitaria Químico Farmacéutico Biólogo, Ingeniería Biomédica, Medicina, Ingeniería Química o experiencia práctica en procesos regulatorios, Dos a tres años de experiencia relevante trabajando con asuntos regulatorios en empresas de dispositivos médicos en Argentina, Inglés Avanzado, Experiencia realizando/validando renovaciones y modificaciones de Registros Sanitarios, Experiencia trabajando con entidades de gobierno como COFEPRIS (México), ANMAT (Argentina) & DIGEMID (Perú)", "qualificationsPreferred" : "Experiencia en registros sanitarios de dispositivos médicos, Experiencia en Auditorías internas y externas / CAPA, Certificados de Buenas prácticas (GMP, GDP) & ISO 13485", "remoteFriendly" : false, "workSiteFlexibility" : "Hybrid", "rawDescription" : "At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. # **A Day in the Life** Somos líderes en tecnología y soluciones médicas impulsados por una misión, con un legado de integridad e innovación. Trabaja con nosotros para incentivar una mejor atención al paciente y colabora con toda la industria para que la asistencia sanitaria sea más asequible y accesible. Forma parte de una comunidad de expertos comprometidos con garantizar una asistencia sanitaria de calidad y asequible en todo el mundo. Venga a fortalecer sus habilidades especializadas y a mejorar su experiencia. Le apoyaremos con la formación, la tutoría, la orientación y las redes que necesita para avanzar, y le capacitaremos para que trabaje de la manera que más le convenga. Juntos, podemos afrontar los retos que cambiarán el panorama de la asistencia sanitaria. Únase a nosotros para desarrollar una carrera que cambia vidas. El puesto estará ubicado en Argentina CABA en un modelo híbrido. **Las responsabilidades pueden incluir las siguientes y se pueden asignar otras tareas:** * Dirige o lleva a cabo la coordinación y preparación de los expedientes de documentación para las presentaciones reglamentarias de todas las áreas de la empresa, así como para las auditorías e inspecciones internas. * Dirige o recopila todos los materiales necesarios para las presentaciones, la renovación de licencias y los registros anuales. * Recomienda cambios en el etiquetado, la fabricación, la comercialización y los protocolos clínicos para garantizar el cumplimiento normativo. * Supervisa y mejora los sistemas de seguimiento y control. * Se mantiene al día de los procedimientos y cambios normativos. * Puede dirigir la interacción con las agencias reguladoras en asuntos definidos. * Recomienda estrategias para la aprobación lo más temprana posible de las solicitudes de ensayos clínicos. **Conocimientos y experiencia requeridos:** * Carrera universitaria de Químico Farmacéutico Biólogo, Ingeniería Biomédica, Medicina, Ingeniería Química y/o experiencia práctica en procesos regulatorios. * Dos a tres años de experiencia relevante trabajando con asuntos regulatorios en empresas de dispositivos médicos en Argentina * Inglés Avanzado * Experiencia realizando/ validando, renovaciones & modificaciones de Registros Sanitarios * Experiencia trabajando con entidades de gobierno como COFEPRIS (México), ANMAT (Argentina) & DIGEMID (Perú) * Sería una ventaja contar con experiencia en registros * sanitarios de dispositivos médicos * Sería una ventaja contar con experiencia en Auditorías internas y externas / CAPA (Corrective and Preventive Actions) * Sería una ventaja contar con certificados de Buenas prácticas (GMP, GDP) & ISO 13485 * Ubicación de la vacante: Argentina CABA **Physical Job Requirements** The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. # **Benefits & Compensation** **Medtronic offers a competitive Salary and flexible Benefits Package** A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). # **About Medtronic** # We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. Learn more about our business, mission, and our commitment to diversity [here](http://www.medtronic.com)", "summaryDescription" : "Regulatory Affairs Specialist at Medtronic. Skills: Regulatory Affairs, Medical Devices, Argentina Regulations. Coordinate and prepare documentation for regulatory submissions. Prepare documentation for internal audits and inspections", "postedDate" : "2026-06-12T08:09:04.116", "createdAt" : "2026-06-12T08:09:03.870", "lastUpdated" : "2026-06-14T22:21:27.909", "ingestTimestamp" : "2026-06-12T08:09:03.870", "mongoId" : "6a2b975674d8ee00a0816d18", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://medtronic.wd1.myworkdayjobs.com/RedeploymentMedtronicCareers/job/Buenos-Aires-Ciudad-Autnoma-de-Buenos-Aires-Argentina/Regulatory-Affairs-Specialist--Argentina_R67027", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Regulatory filing", "Validation", "Modification", "Registration", "Audit", "CAPA", "Leadership", "Regulatory Affairs", "Medical Devices", "Argentina Regulations", "Regulatory affairs", "Documentation preparation", "Regulatory submissions", "License renewal", "Annual registrations", "Labeling changes", "Manufacturing changes", "Marketing changes", "Clinical protocols", "Regulatory compliance", "Tracking systems", "Control systems", "Regulatory procedures", "Regulatory changes", "Agency interaction", "Clinical trial applications", "Medical devices", "Argentinian regulations", "COFEPRIS", "ANMAT", "DIGEMID", "Good Practices", "ISO 13485", "GMP", "GDP" ], "skillCount" : 35, "jobCategory" : "other", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "id" : "6a2c937674d8ee00a09881e4", "title" : "Associate, Government Affairs", "company" : "Oscar Health", "industry" : "Insurance", "salary" : { "min" : 96876.0, "max" : 127149.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "New York, New York, United States", "locations" : [ "New York", "New York", "United States" ], "timestamp" : "2026-06-15T12:22:55.813", "fingerprint" : "faa5c3ead3546bf22ae6307e4e8b868f9796fa5489ae4d26bea4980000b949a5", "source" : "greenhouse", "language" : "en", "applyUrl" : "http://www.hioscar.com/careers/7974658?gh_jid=7974658", "externalId" : "7974658", "industryFunction" : { }, "structuredLocations" : [ { "city" : "New York", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "40.7127281,-74.0060152" } ], "locationText" : "New York, New York, United States", "employmentType" : "FULL_TIME", "professionalSkills" : [ "Regulatory analysis", "Policy analysis", "Legal analysis", "Risk management", "Compliance oversight" ], "hardSkillsList" : [ "Legislative tracking", "Regulatory tracking", "Drafting summaries", "Client-focused memoranda" ], "hardSkills" : [ { "name" : "Legislative tracking", "level" : "intermediate" }, { "name" : "Regulatory tracking", "level" : "intermediate" }, { "name" : "Drafting summaries", "level" : "intermediate" }, { "name" : "Client-focused memoranda", "level" : "intermediate" } ], "majorSkills" : "Government affairs, Regulatory guidance, Public policy", "majorSkillsList" : [ "Government affairs", "Regulatory guidance", "Public policy" ], "coreResponsibilities" : "Communicate legislation, Communicate regulations, Communicate bulletins, Communicate regulatory guidance, Track legislative developments, Track regulatory developments, Draft summaries, Communicate client-focused memoranda, Advise business impact, Support trade association relationships, Cover legislative hearings, Cover regulatory hearings, Cover legislative meetings, Cover regulatory meetings, Serve as enterprise resource, Identify laws, Track laws, Identify regulations, Track regulations, Prepare summaries, Prepare analyses, Assist company implementation, Present policy developments, Digest developments, Communicate developments, Support sustainable processes, Simplify team outputs, Ensure high quality deliverables, Deliver assignments, Adhere to deadlines, Manage competing priorities", "teamCollaboration" : "Government Affairs Counsel; PRO Counsel; Government Affairs colleagues; Cross functional business partners; Compliance team", "domainKnowledge" : "Health plan; Managed care; State policy; Public policy; Legislative trends; Regulatory trends; Affordable Care Act", "domainList" : [ "health-plan", "managed-care", "state-policy", "public-policy", "legislative-trends", "regulatory-trends", "affordable-care-act" ], "domainSpecificKnowledge" : [ "Health plan", "Managed care", "State policy", "Public policy", "Legislative trends", "Regulatory trends", "Affordable Care Act" ], "toolProficiency" : [ "Westlaw", "Google Workspace" ], "communicationSkills" : "Present to internal audiences; Communicate legislative developments; Communicate regulatory developments", "documentationSkills" : "Draft summaries; Prepare summaries; Prepare analyses; Draft memoranda", "qualificationsBasic" : "Bachelor's degree, 3+ years legal experience, 3+ years regulatory experience, 2+ years state political experience, 2+ years legislative process experience, 2+ years Westlaw experience, 2+ years legislative tracking software experience, 2+ years Google Workspace experience", "qualificationsPreferred" : "Familiarity with Affordable Care Act", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Hi, we're Oscar. We're hiring an Associate, Government Affairs to join our Government Affairs. Oscar is the first health insurance company built around a full stack technology platform and a relentless focus on serving our members. We started Oscar in 2012 to create the kind of health insurance company we would want for ourselves—one that behaves like a doctor in the family. About the role: The Associate, Government Affairs, is a major contributor and owner of mission critical workflows to communicate proposed and enacted legislation, regulations, bulletins, and other regulatory guidance to impacted business units. In assigned jurisdictions, the Associate, Government Affairs will track legislative and regulatory developments, draft summaries of high priority items, and communicate client-focused memoranda to Oscar’s compliance team advising of business impact upon passage. The Associate, Government Affairs supports the Government Affairs Counsel in trade association relationships, cover pertinent legislative and regulatory hearings and meetings as assigned, and supports the Government Affairs function by serving as an enterprise wide resource on public policy and legislative and regulatory trends. You will report into the Manager of Government and Regulatory Affairs. Work Location: This position is based in our New York City office, requiring a hybrid work schedule with 3 days of in-office work per week. Thursdays are a required in-office day for team meetings and events, while your other two office days are flexible to suit your schedule. #LI-Hybrid Pay Transparency: The base pay for this role is: $96,876.00 - $127,149.75 per year. You are also eligible for employee benefits, participation in Oscar's unlimited vacation program and annual performance bonuses. Responsibilities: Serve as the subject matter expert on assigned state policy and legislative matters, while identifying and tracking newly proposed and effective laws and regulations in assigned jurisdictions. With support from Government Affairs Counsel, prepare clear, concise, user friendly summaries and analyses based upon client needs of newly effective laws and regulations and assist with company implementation. Present to internal audiences in appropriate forums on priority legislative and regulatory policy developments. Partner with PRO Counsel, Government Affairs colleagues, and cross functional business partners to clearly digest and communicate legislative, regulatory and subregulatory developments. Support sustainable processes which simplify our growing team’s outputs while ensuring high quality deliverables. Deliver multiple, simultaneous and diverse assignments while adhering to deadlines and managing competing priorities in a fast-paced environment. Requirements: Bachelor’s degree in legal studies, political science, public policy, public administration, public health or other relevant field, or a combination of education and experience. 3+ years of legal or regulatory experience, ideally in the health plan/managed care space. 2+ years experience working with state political and legislative processes. 2+ years experience in Westlaw, legislative tracking software, and Google Workspace. Bonus points: Familiarity with the Affordable Care Act and Healthcare.gov or other State Based Exchanges. Experience with Oscar markets. Experience working with attorneys and internal stakeholders. This is an authentic Oscar Health job opportunity. Learn more about how you can safeguard yourself from recruitment fraud here. At Oscar, being an Equal Opportunity Employer means more than upholding discrimination-free hiring practices. It means that we cultivate an environment where people can be their most authentic selves and find both belonging and support. We're on a mission to change health care -- an experience made whole by our unique backgrounds and perspectives. Pay Transparency: Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education, and experience. Full-time employees are eligible for benefits including: medical, dental, and vision benefits, 11 paid holidays, paid sick time, paid parental leave, 401(k) plan participation, life and disability insurance, and paid wellness time and reimbursements. Artificial Intelligence (AI): Our AI Guidelines outline the acceptable use of artificial intelligence for candidates and detail how we use AI to support our recruiting efforts. Reasonable Accommodation: Oscar applicants are considered solely based on their qualifications, without regard to applicant’s disability or need for accommodation. Any Oscar applicant who requires reasonable accommodations during the application process should contact the Oscar Benefits Team (accommodations@hioscar.com) to make the need for an accommodation known. California Residents: For information about our collection, use, and disclosure of applicants’ personal information as well as applicants’ rights over their personal information, please see our Privacy Policy.", "summaryDescription" : "Associate, Government Affairs at Oscar Health. Skills: Government affairs, Regulatory guidance, Public policy. Communicate legislation. Communicate regulations", "postedDate" : "2026-06-14T09:12:49.848", "createdAt" : "2026-06-14T09:12:49.848", "lastUpdated" : "2026-06-15T12:22:55.813", "ingestTimestamp" : "2026-06-14T09:12:49.848", "mongoId" : "6a2c937674d8ee00a09881e4", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 96876, "salaryAnnualMax" : 127149, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Legislative tracking", "Regulatory tracking", "Drafting summaries", "Client-focused memoranda", "Government affairs", "Regulatory guidance", "Public policy", "Regulatory analysis", "Policy analysis", "Legal analysis", "Risk management", "Compliance oversight", "Health plan", "Managed care", "State policy", "Legislative trends", "Regulatory trends", "Affordable Care Act", "Westlaw", "Google Workspace" ], "skillCount" : 20, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Junior", "dataQualityScore" : 0.8888889, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c934374d8ee00a0987c0f", "title" : "Staff Digital Sculptor", "company" : "Ōura", "industry" : "Technology", "salary" : { "min" : 350000.0, "max" : 550000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimation is based on market data for a Staff Digital Sculptor in San Francisco, USA, adjusted for executive seniority and the technology industry." }, "location" : "San Francisco, CA, United States", "locations" : [ "San Francisco", "CA", "United States" ], "timestamp" : "2026-06-15T06:39:01.424", "fingerprint" : "91fbfa8fa21ec7aad138a652e80416e92f79d473f4b6cd63ecae30b9ba1c9a05", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/oura/jobs/4208422009", "externalId" : "4208422009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "San Francisco", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "37.7879363,-122.4075201" } ], "locationText" : "San Francisco, California, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 10, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "3D CAD, 3D modeling, Visualization", "professionalSkills" : [ "Design intent translation", "Surfacing techniques", "Product development workflows", "Design optimization" ], "hardSkillsList" : [ "3D surfacing", "Photorealistic rendering", "Surface development" ], "hardSkills" : [ { "name" : "3D surfacing", "level" : "intermediate" }, { "name" : "Photorealistic rendering", "level" : "intermediate" }, { "name" : "Surface development", "level" : "intermediate" } ], "majorSkills" : "3D modeling, Visualization, Surface development", "majorSkillsList" : [ "3D modeling", "Visualization", "Surface development" ], "coreResponsibilities" : "Translate design intent, Sculpt complex forms, Develop high-fidelity visualizations, Communicate product concepts, Optimize models for prototyping, Optimize models for manufacturing, Iterate based on feedback, Contribute to design language, Enhance modeling efficiency, Enhance visualization quality", "teamCollaboration" : "Industrial design teams; Engineering teams; Manufacturing teams; Cross-functional environment", "domainKnowledge" : "Industrial design principles; Product development workflows; Manufacturing processes", "domainList" : [ "industrial-design-principles", "product-development-workflows", "manufacturing-processes" ], "domainSpecificKnowledge" : [ "Industrial design principles", "Product development workflows", "Manufacturing processes" ], "toolProficiency" : [ "Autodesk Alias", "Siemens NX", "Keyshot", "Substance" ], "innovationCreativity" : "Creativity", "problemSolvingSkills" : "Solve complex design challenges", "qualificationsBasic" : "10+ years advanced 3D CAD, Expert Keyshot experience, Solid industrial design foundation, In-depth manufacturing knowledge, Highly detailed 3D models, Prepare 3D models for prototyping, Communication and collaboration skills", "qualificationsPreferred" : "Familiarity with Substance", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Our mission at Oura is to empower every person to own their inner potential. Our award-winning products help our global community gain a deeper knowledge of their readiness, activity, and sleep quality by using their Oura Ring and its connected app. We've helped millions of people understand and improve their health by providing daily insights and practical steps to inspire healthy lifestyles. Empowering the world starts with living our values and empowering our team. As a quickly growing company focused on helping people live healthier and happier lives, we ensure that our team members have what they need to do their best work — both in and out of the office. We’re looking for a talented and passionate Staff Digital Sculptor to join our forward-thinking team. In this role, you’ll play a key part in bringing next-generation hardware designs to life—bridging the gap between visionary industrial design and production-ready reality through world-class 3D modeling and visualization, and influencing the technical direction of the team. What you will do: Partner closely with industrial design, engineering, and manufacturing teams to translate design intent into precise, high-quality 3D CAD models. Apply advanced surfacing techniques to sculpt complex forms that maintain aesthetic excellence and support manufacturability. Develop high-fidelity visualizations and photorealistic renderings that clearly communicate product concepts and features. Leverage your deep understanding of design principles and production methods to ensure models are optimized for prototyping and manufacturing. Iterate quickly and thoughtfully based on feedback, with a keen eye for precision and detail. Contribute to the evolution of our design language through craftsmanship, creativity, and technical mastery. Contribute to the development and implementation of new tools, workflows, and technologies to enhance modeling and visualization efficiency and quality. This is a hybrid-remote role, with the expectation to work from our San Francisco offices at least half-time. REQUIREMENTS We would love consider you for our role if you have: 10 yrs + experience in advanced 3D CAD tools, including Autodesk Alias and Siemens NX. Expert level experience with Keyshot or similar rendering/visualization tools. Strong familiarity with Substance or other material/texture creation software is a strong plus. A solid foundation in industrial design principles and product development workflows, with an ability to anticipate and solve complex design challenges. In-depth knowledge of manufacturing processes and their impact on 3D modeling and surface development, and the ability to proactively optimize designs for production. Exceptional skill in creating highly detailed, accurate, and production-ready 3D models. A comprehensive portfolio that showcases your mastery in 3D modeling, surfacing, and visualization for product design, demonstrating significant contributions to shipped products. Strong experience preparing 3D models for rapid prototyping or tooling. Strong communication and collaboration skills—able to thrive in a fast-paced, cross-functional environment. A passion for cutting-edge technology and designing products that make a difference in people’s lives. BENEFITS At Oura, we care about you and your well-being. Everyone here at Oura has a ring of their own and we are continually looking to improve employee health and add to our benefits! What we offer: Competitive salary and equity packages Health, dental, vision insurance, and mental health resources An Oura Ring of your own plus employee discounts for friends & family 20 days of paid time off plus 13 paid holidays plus 8 days of flexible wellness time off Paid sick leave and parental leave Amazing culture of collaborative and passionate coworkers Oura takes a market-based approach to pay, which may vary depending on your location. US locations are categorized into tiers based on a cost of labor index for that geographic area. While most offers will be closer to the starting range, successful candidates' pay will be determined based on job-related skills, experience, qualifications, work location, internal peer equity, and market conditions. These ranges may be modified in the future. Region 1: $198,050 - $233,000 A recruiter can determine your zones/tiers based on your US location. We are not considering candidates residing in the following states: Alaska (AK), Arkansas (AR), Delaware (DE), Iowa (IA), Mississippi (MS), Nebraska (NE), Oklahoma (OK), Rhode Island (RI), South Dakota (SD), Vermont (VT), West Virginia (WV), and Wisconsin (WI) Oura is proud to be an equal opportunity workplace. We celebrate diversity and are committed to creating an inclusive environment for all employees. Individuals seeking employment at Oura are considered without regard to age, ancestry, color, gender (including pregnancy, childbirth, or related medical conditions), gender identity or expression, genetic information, marital status, medical condition, mental or physical disability, national origin, protected family care or medical leave status, race, religion (including beliefs and practices or the absence thereof), sexual orientation, military or veteran status, or any other characteristic protected by federal, state, or local laws. We will not tolerate discrimination or harassment based on any of these characteristics. We will work to ensure individuals with disabilities are provided reasonable accommodation to participate in the interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Disclaimer: Beware of fake job offers! We’ve been alerted to scammers posing as ŌURA recruiters, especially for remote roles. Please note: Our jobs are listed only on the ŌURA Careers page and trusted job boards. We will never ask for personal information like ID or payment for equipment upfront. Official offers are sent through Docusign after a verbal offer, not via text or email. Stay cautious and protect your personal details. To all recruitment agencies: Oura does not accept agency resumes. Please do not forward resumes to our jobs alias, Oura employees, or any other organization's location. Oura is not responsible for any fees related to unsolicited resumes.", "summaryDescription" : "Staff Digital Sculptor at Ōura. Skills: 3D modeling, Visualization, Surface development. Translate design intent. Sculpt complex forms", "postedDate" : "2026-06-13T22:19:29.159", "createdAt" : "2026-06-13T22:19:29.159", "lastUpdated" : "2026-06-15T06:39:01.424", "ingestTimestamp" : "2026-06-13T22:19:29.159", "mongoId" : "6a2c934374d8ee00a0987c0f", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 350000, "salaryAnnualMax" : 550000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "3D surfacing", "Photorealistic rendering", "Surface development", "3D modeling", "Visualization", "Design intent translation", "Surfacing techniques", "Product development workflows", "Design optimization", "Industrial design principles", "Manufacturing processes", "Autodesk Alias", "Siemens NX", "Keyshot", "Substance" ], "skillCount" : 15, "jobCategory" : "product", "jobSubcategory" : "design", "seniorityLevel" : "Executive", "dataQualityScore" : 1.0, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.95 }, { "id" : "694ae6ce70f0b99d589b27fc", "title" : "Regulatory Complaints Associate", "company" : "Hyundai Capital America", "industry" : "Banking", "salary" : { "min" : 65000.0, "max" : 95000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline data for a Mid-level Regulatory Complaints Associate in Irvine, United States, adjusted for the Financial Services industry and company size." }, "location" : "United States-California-Irvine", "locations" : [ "United States-California-Irvine", "
Headquarters 1 (HCA_HQ1)
3161 Michelson Dr. Ste 1900
Irvine, 92612

" ], "timestamp" : "2026-06-16T05:29:45.452", "fingerprint" : "3035ccd28190e3758a69a0e4fe5f0509d96ea47fc2283f34be3e5b2165b00cdf", "source" : "taleo", "language" : "en", "applyUrl" : "https://hyundaicapital.taleo.net/careersection/ex/jobdetail.ftl?job=105943", "externalId" : "105943", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Irvine", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "33.6856969,-117.8259810" } ], "locationText" : "Irvine, California, United States", "professionalSkills" : [ "Risk management", "Legal analysis", "Compliance oversight" ], "hardSkillsList" : [ "Regulatory requirements" ], "hardSkills" : [ { "name" : "Regulatory requirements", "level" : "intermediate" } ], "majorSkills" : "Regulatory requirements, Risk management, Legal analysis, Compliance oversight", "majorSkillsList" : [ "Regulatory requirements", "Risk management", "Legal analysis", "Compliance oversight" ], "coreResponsibilities" : "Oversee regulatory compliance, Manage legal risks, Analyze regulatory requirements, Ensure compliance oversight", "domainKnowledge" : "Regulatory compliance; Risk management; Legal analysis", "domainList" : [ "regulatory-compliance", "risk-management", "legal-analysis" ], "domainSpecificKnowledge" : [ "Regulatory compliance", "Risk management", "Legal analysis" ], "remoteFriendly" : false, "rawDescription" : "Who We Are Through our service brands Hyundai Motor Finance, Genesis Finance, and Kia Finance, Hyundai Capital America offers a wide range of financial products tailored to meet the needs of Hyundai, Genesis, and Kia customers and dealerships. We provide vehicle financing, leasing, subscription, and insurance solutions to over 2 million consumers and businesses. Embodying our commitment to grow, innovate, and diversify, we strive to reimagine the customer and dealer experience and launch innovative new products that broaden our market reach. We believe that success comes from within and are proud to support our team members through skill development and career advancement. Hyundai Capital America is an Equal Opportunity Employer committed to creating a diverse and inclusive culture for our workforce. We are a values-driven company dedicated to supporting both internal and external communities through volunteering, philanthropy, and the empowerment of our Employee Resource Groups. Together, we strive to be the leader in financing freedom of movement. We Take Care of Our People Along with competitive pay, as an employee of HCA, you are eligible for the following benefits: ·          Medical, Dental and Vision plans that include no-cost and low-cost plan options ·          Immediate 401(k) matching and vesting ·          Vehicle purchase and lease discounts plus monthly vehicle allowances ·          Paid Volunteer Time Off with company donation to a charity of your choice ·          Tuition reimbursement What to Expect The Regulatory Complaints Associate is responsible on a daily basis for drafting comprehensive responses to customer complaints submitted through HCA’s regulators in accordance with the applicable statutory timeline. What You Will Do 1.      Regulatory Complaint Daily Activity ·          Draft and review other responses to complaints received through the Consumer Financial Protection Bureau (CFPB) and state regulators, including working with HCA’s CARE Team to obtain research, validation of research, preparation, and submission of responses. ·          Monitor the State Examination System complaint portal on a daily basis to obtain and respond accurately, thoroughly and timely to regulator complaints. ·          Identify potential regulatory risks while responding to complaints ·          Formulate recommendations and escalate internally, as needed. ·          Serve as a point of contact for state regulators regarding complaints, working directly with state regulators to respond to complaints and resolve escalated regulatory complaint issues. ·          Document accounts and include all relevant information and documents. 2.      Complaint Analysis and Review ·          Assist in analyzing regulatory complaint data, including completing reviews of internal complaints identified as potentially being regulatory in nature, and preparing recaps of regulatory complaints where the driver is HCA Error. ·          Complete high risk complaint category reviews and provide feedback to the business on any issues or opportunities identified. Develop remediation and training plans to be presented to management for implementation by the business to reduce complaint volume. 3.      Reporting ·          Assist in analyzing regulatory complaint data ·          Assist in preparing and distributing monthly, quarterly and ad-hoc report summaries related to regulator complaints. What You Will Bring ·          Minimum 2-4 years related experience in escalated customer complaints. ·          Experience in the auto finance industry a plus. ·          Bachelor’s degree or equivalent work experience required. ·          Strong problem solving and analytical skills to successfully address regulator complaints, perform root cause analysis and identify trends. ·          Excellent communication skills, written and verbal, with the ability to effectively communicate with all levels in the organization and external state regulator personnel. ·          Strong attention to detail. ·          Knowledge of applicable federal regulations and general compliance concepts. ·          Proficient with Microsoft Office (Word, Excel, PowerPoint) ·          Demonstrated ability to learn systems and processes. Work Environment Employees in this class are subject to extended periods of sitting, standing and walking, and using a computer. Work is performed in an office environment. The posted salary range for this job takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; geographic location, and other business and organizational needs. Successful candidates may be hired anywhere in the salary range based on these factors. It is uncommon to hire candidates at or near the top of the range. California Privacy Notice This notice only applies to our applicants who reside in the State of California. The latest version of our Privacy Policy can be found here . This Privacy Policy provides you with notice, at or before the point of collection, about the categories of personal information to be collected from you, the purposes for which your personal information is collected or used, and whether that information is sold or shared, so that you can exercise meaningful control over our use of your personal information. We are providing this notice to comply with the California Consumer Privacy Act of 2018, as amended as amended by the California Privacy Rights Act of 2020 (“CCPA”). If you have any questions about CCPA regarding California residents or HCA team members, please contact the Privacy Team at Privacy2@hcs.com . United States-California-Irvine", "summaryDescription" : "Regulatory Complaints Associate at Hyundai Capital America. Skills: Regulatory requirements, Risk management, Legal analysis, Compliance oversight. Oversee regulatory compliance. Manage legal risks", "createdAt" : "2026-06-14T18:52:14.313", "lastUpdated" : "2026-06-16T05:29:45.452", "ingestTimestamp" : "2026-06-14T18:52:14.313", "mongoId" : "694ae6ce70f0b99d589b27fc", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 65000, "salaryAnnualMax" : 95000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Regulatory requirements", "Risk management", "Legal analysis", "Compliance oversight", "Regulatory compliance" ], "skillCount" : 5, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Mid", "dataQualityScore" : 0.6666667, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Financial Services", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2a5ca074d8ee00a061551f", "title" : "Regulatory Affairs Intern", "company" : "EnergyHub", "industry" : "Energy", "salary" : { "min" : 24.0, "max" : 25.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Brooklyn, New York", "locations" : [ "Brooklyn", "New York" ], "timestamp" : "2026-06-14T22:16:31.405", "fingerprint" : "a9daa04b0d1993e56837022d277622c1ee5fccc80a0d10b5abfa01dc3ef675f1", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/energyhub/jobs/8562493002", "externalId" : "8562493002", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Brooklyn", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.6526006,-73.9497211" } ], "locationText" : "Brooklyn, New York, United States", "employmentType" : "INTERNSHIP", "experienceMinYears" : 0, "experienceMaxYears" : 2, "experienceLevel" : "Entry", "professionalSkills" : [ "Policy strategy", "Regulatory strategy" ], "hardSkillsList" : [ "Research" ], "softSkillsList" : [ "Analytical thinking" ], "hardSkills" : [ { "name" : "Research", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Analytical thinking" } ], "majorSkills" : "Regulatory affairs, Clean energy policy", "majorSkillsList" : [ "Regulatory affairs", "Clean energy policy" ], "coreResponsibilities" : "Support policy work, Support regulatory strategy, Contribute to research, Contribute to strategy development, Share cross-functional information", "teamCollaboration" : "Cross-functional information sharing", "domainKnowledge" : "Distributed energy resources; Virtual power plants; Grid modernization", "domainList" : [ "distributed-energy-resources", "virtual-power-plants", "grid-modernization" ], "domainSpecificKnowledge" : [ "Distributed energy resources", "Virtual power plants", "Grid modernization" ], "remoteFriendly" : false, "rawDescription" : "About EnergyHub EnergyHub is a leading provider of distributed energy resource (DER) management solutions that help utilities unlock the full potential of virtual power plants (VPPs). By connecting and optimizing customer-owned devices like smart thermostats, EV chargers, and batteries. EnergyHub enables a cleaner, more flexible, and more reliable grid. EnergyHub empowers utilities and their customers to create a clean, distributed energy future. We help consumers turn their smart thermostats, EVs, batteries, and other products into virtual power plants that keep the grid stable and enable higher penetration of solar and wind power. Role Overview: EnergyHub is seeking a motivated and analytically minded Regulatory Affairs Intern to support our policy and regulatory strategy work. This role offers hands-on experience at the intersection of clean energy policy, grid modernization, and technology. The intern will contribute to research, strategy development, and cross-functional information sharing that supports EnergyHub’s VPP business across the U. S. Key Project Areas 401(k) or other retirement programs; paid time off; company-paid holidays; equity; bonuses; or commissions. Interns are eligible for any benefits required by applicable state or local law, including paid sick leave in jurisdictions that mandate it (such as Colorado, Washington, California, and New York City). To apply, please submit your application here or go to EnergyHub.com/careers. Hourly Rate $24—$25 USD", "summaryDescription" : "Regulatory Affairs Intern at EnergyHub. Skills: Regulatory affairs, Clean energy policy. Support policy work. Support regulatory strategy", "postedDate" : "2026-06-11T21:29:39.029", "createdAt" : "2026-06-11T21:29:39.029", "lastUpdated" : "2026-06-14T22:16:31.405", "ingestTimestamp" : "2026-06-11T21:29:39.029", "mongoId" : "6a2a5ca074d8ee00a061551f", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 49920, "salaryAnnualMax" : 52000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Research", "Analytical thinking", "Regulatory affairs", "Clean energy policy", "Policy strategy", "Regulatory strategy", "Distributed energy resources", "Virtual power plants", "Grid modernization" ], "skillCount" : 9, "jobCategory" : "sales", "jobSubcategory" : "sales", "dataQualityScore" : 1.0, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Energy" }, { "id" : "693072a570f0b99d58ffb691", "title" : "Senior Lead, Regulatory Affairs, APAC", "company" : "Amazon Kuiper", "industry" : "Public Policy, alexa and amazon devices", "salary" : { "min" : 220000.0, "max" : 315000.0, "currency" : "AUD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Senior Lead, Regulatory Affairs, APAC in Sydney, Australia, adjusted for seniority, company size, and the technology industry." }, "location" : "Sydney, New South Wales, AUS", "locations" : [ "Sydney, New South Wales, AUS" ], "timestamp" : "2026-06-15T02:36:45.003", "fingerprint" : "73fb7d1248c5e0357989800e64f7760320799cfee1d8639734145ae7e456d68a", "source" : "amazon", "language" : "en", "applyUrl" : "https://account.amazon.com/jobs/3135613/apply", "externalId" : "2bd8a393-c06e-4275-b5aa-b111fcc6a617", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Sydney", "state" : "New South Wales", "country" : "Australia", "continent" : "oc", "source" : "llm", "workMode" : "onsite", "geo" : "-33.8698439,151.2082848" } ], "locationText" : "Sydney, New South Wales, Australia", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Regulatory affairs", "Compliance strategy", "Advocacy", "Public policy", "Regulatory filings", "Communications regulation" ], "hardSkillsList" : [ "Communications regulation", "Regulatory compliance", "Export control laws", "Export Administration Regulations" ], "hardSkills" : [ { "name" : "Communications regulation", "level" : "intermediate" }, { "name" : "Regulatory compliance", "level" : "intermediate" }, { "name" : "Export control laws", "level" : "intermediate" }, { "name" : "Export Administration Regulations", "level" : "intermediate" } ], "majorSkills" : "Regulatory affairs, Compliance, APAC region, Telecommunications regulation", "majorSkillsList" : [ "Regulatory affairs", "Compliance", "APAC region", "Telecommunications regulation" ], "coreResponsibilities" : "Interface directly with regulators, Perform advocacy consistent with priorities, Develop and optimize mechanisms for filing, Ensure accurate and timely filing, Align with Regulatory, Compliance, Legal, Public Policy, and, Drive timely and accurate compliance filings, Address unique nature of operating as a CSP, Communicate with regulators on compliance matters, Shape national, regional and international regulations, Define and lead regulatory compliance agenda, Collaborate to shape rules and regulations, Enhance overall regulatory compliance strategy, Ensure alignment on country and regional basis, Anticipate bottlenecks, Communicate risks clearly to leaders, Escalate effectively, Remove blockers, Deliver results", "teamCollaboration" : "Align with Regulatory, Compliance, Legal, Public Policy; Work with business, technical and operations teams; Work with Public Policy, Public Relations and Legal teams; Work with regulatory country leads; Work with Technical Program Managers; Coordinate across Amazon Leo's entities; Coordinate across Amazon at large", "domainKnowledge" : "Communications regulation; NGSO communications systems; Satellite orbital; Radio frequency spectrum; Export control laws; Export Administration Regulations", "domainList" : [ "communications-regulation", "ngso-communications-systems", "satellite-orbital", "radio-frequency-spectrum", "export-control-laws", "export-administration-regulations" ], "domainSpecificKnowledge" : [ "Communications regulation", "NGSO communications systems", "Satellite orbital", "Radio frequency spectrum", "Export control laws", "Export Administration Regulations" ], "communicationSkills" : "External point of contact; Advocacy; Communicate risks", "documentationSkills" : "Complex compliance filings; Regulatory filings", "problemSolvingSkills" : "Anticipate bottlenecks; Remove blockers", "specialRequirements" : "Subject to export control laws, Obtain export licenses or approvals", "outcomesObjectives" : "Deliver fast, affordable and reliable internet connectivity; Advance regulatory interests; Ensure scalability; Allow service; Benefit our customers", "qualificationsBasic" : "Bachelor's degree or above, Experience in public policy and advocacy", "qualificationsPreferred" : "12+ years of working directly with government officials and regulatory bodies experience", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Amazon Leo is Amazon’s low Earth orbit (LEO) satellite network. Our mission is to deliver fast, affordable and reliable internet connectivity to customers beyond the reach of existing networks. From individual households to schools, hospitals, businesses, and government agencies, Amazon Leo will serve people and organizations operating in locations without reliable connectivity. The Senior Lead, Regulatory Affairs, APAC will be the external point of contact for Amazon Leo’s service compliance obligation deliverables in front of telecommunications regulators and other stakeholders in countries throughout the APAC region. This role will use their specific knowledge of communications regulation to advance Amazon Leo’s regulatory interests by coordinating complex compliance filings, maintaining effective lines-of-communication with relevant regulatory bodies and policy makers, and developing mechanisms to ensure scalability. This position may require access to information, technology, or hardware that is subject to export control laws and regulations, including the Export Administration Regulations (EAR) and the International Traffic in Arms Regulations (ITAR). Employment in this position is contingent upon obtaining any required export licenses or other approvals from the United States government. As such, the successful candidate must be eligible to obtain any necessary export licenses or approvals based on their nationality, citizenship, and any other factors considered by the applicable export control regulations. Key job responsibilities Key job responsibilities include: * Interface directly with regulators and policy makers in countries throughout the APAC region to drive Amazon Leo's compliance strategy and perform advocacy consistent with Amazon Leo’s priorities. * Develop and optimize mechanisms to ensure accurate and timely filing of complex Communications Service Provider (CSP) compliance filings. * Align with Regulatory, Compliance, Legal, Public Policy, and Global Expansions on strategy for CSP compliance matters. * Drive timely and accurate compliance filings related to regulatory obligations that arise as a result of Amazon Leo’s status as a CSP (e.g., revenue reporting, subscriber reports, outage reporting, customer complaints, etc.). * Coordinate across Amazon Leo's entities, and across Amazon at large, to address the unique nature of Amazon Leo's operating as a CSP. A day in the life You will be responsible for communicating with regulators and other stakeholders on regulatory compliance matters, shaping national, regional and international regulations affecting NGSO communications systems. You will define and lead the regulatory compliance agenda to allow service, and collaborate with trade associations, government agencies, multilateral organizations, and other operators to shape rules and regulations in the best interest of our customers. You will work with business, technical and operations teams, as well as with Public Policy, Public Relations and Legal teams, to enhance the overall regulatory compliance strategy in priority countries, and work closely with regulatory country leads, Technical Program Managers (TPMs), and other teams to ensure alignment on a country and regional basis. You will anticipate bottlenecks and communicate risks clearly to leaders, escalating effectively, removing blockers, and delivering results. About the team The Regulatory team enables and protects Amazon Leo’s use of radio frequency spectrum and satellite orbital worldwide, defining and leading the regulatory agenda to benefit our customers. We operate globally, engaging with international, regional/sub-regional regulatory organizations, regulatory authorities, and governments. We obtain and maintain the required ITU filings and licenses for Amazon Leo's operations, coordinate spectrum use with other operators, and shape/promote space safety and sustainability. We are responsible for the licensing of facilities and services, and advocate for rules and regulations in the best interest of our customers, working with governments, trade associations, and operators. We work with the design, operational, and business teams to promote alignment between business objectives, the Program of Record, and regulatory and compliance requirements for delivery of service. Basic Qualifications: - Bachelor's degree or above in a relevant discipline (e.g. Law, Political Science, Public Policy, Public Affairs, Economic Development) - Experience in relevant public policy and advocacy on payments and financial services issues Preferred Qualifications: - 12+ years of working directly with government officials and regulatory bodies experience Acknowledgement of country: In the spirit of reconciliation Amazon acknowledges the Traditional Custodians of country throughout Australia and their connections to land, sea and community. We pay our respect to their elders past and present and extend that respect to all Aboriginal and Torres Strait Islander peoples today. IDE statement: Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status. 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" : "Senior Lead, Regulatory Affairs, APAC at Amazon Kuiper. Skills: Regulatory affairs, Compliance, APAC region, Telecommunications regulation. Interface directly with regulators. Perform advocacy consistent with priorities", "postedDate" : "2026-06-13T06:36:16.768", "createdAt" : "2026-06-13T06:36:16.768", "lastUpdated" : "2026-06-15T02:36:45.003", "ingestTimestamp" : "2026-06-13T06:36:16.768", "mongoId" : "693072a570f0b99d58ffb691", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.com/jobs/3135613/apply", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Communications regulation", "Regulatory compliance", "Export control laws", "Export Administration Regulations", "Regulatory affairs", "Compliance", "APAC region", "Telecommunications regulation", "Compliance strategy", "Advocacy", "Public policy", "Regulatory filings", "NGSO communications systems", "Satellite orbital", "Radio frequency spectrum" ], "skillCount" : 15, "jobCategory" : "other", "dataQualityScore" : 1.0, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Telecommunications" }, { "id" : "6a191e7658b93c861e39f679", "title" : "Digital Twin AI", "company" : "Mercedes-Benz Research and Development India", "industry" : "Manufacturing", "salary" : { "min" : 1850000.0, "max" : 2750000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Digital Twin AI role in Bangalore, India, adjusted for the manufacturing industry and company size." }, "location" : "India-Karnataka-Bangalore", "locations" : [ "India-Karnataka-Bangalore", "'Embassy Crest' Plot No 5, , EPIP Zone, Phase 1, " ], "certifications" : [ "AI certifications", "Machine Learning certifications", "Cloud Computing certifications", "Digital Twin certifications", "NVIDIA Omniverse certifications" ], "timestamp" : "2026-06-16T03:12:43.875", "fingerprint" : "47e7c1e68e9457e4af764101938b97310fd699d25191f943bd67d26a619e8bfe", "source" : "taleo", "language" : "en", "applyUrl" : "https://tas-daimler.taleo.net/careersection/ex/jobdetail.ftl?job=897846", "externalId" : "897846", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Bangalore", "state" : "Karnataka", "country" : "India", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "12.9767936,77.5900820" } ], "locationText" : "Bangalore, Karnataka, India", "minimumEducation" : "Bachelor's", "technicalSkills" : "Python, C#, C++, Java, IoT, Data analytics, Cloud computing, Hybrid cloud, Machine learning, Deep learning, Generative AI, NVIDIA Omniverse, 3D content creation, 3ds Max, Maya, Revit, Blender, Substance, 3D geometry, Animation, Materials, GPU", "professionalSkills" : [ "Software development", "Design", "Re-engineering", "Simulation technologies", "AI-driven modeling", "3D workflows", "3D pipelines", "Content creation", "Software technology architecture", "Datacenter architecture" ], "hardSkillsList" : [ "Digital twin development", "Process simulation", "Product development", "SDK development", "Full-stack datacenter architecture" ], "hardSkills" : [ { "name" : "Digital twin development", "level" : "intermediate" }, { "name" : "Process simulation", "level" : "intermediate" }, { "name" : "Product development", "level" : "intermediate" }, { "name" : "SDK development", "level" : "intermediate" }, { "name" : "Full-stack datacenter architecture", "level" : "intermediate" } ], "majorSkills" : "Digital Twin, AI, NVIDIA Omniverse, 3D simulation", "majorSkillsList" : [ "Digital Twin", "AI", "NVIDIA Omniverse", "3D simulation" ], "coreResponsibilities" : "Design digital twin models, Develop digital twin models, Maintain digital twin models, Collaborate with engineering teams, Collaborate with manufacturing teams, Collaborate with product teams, Integrate digital twins, Analyze digital twin data, Identify actionable insights, Optimize manufacturing processes, Improve planning efficiency, Enhance decision-making, Develop 3D workflows, Demonstrate 3D workflows, Design software technology architecture, Develop software technology architecture, Utilize GPUs, Develop SDKs, Develop full-stack datacenter architecture, Monitor emerging trends", "teamCollaboration" : "Cross-functional engineering teams; Cross-functional manufacturing teams; Cross-functional product teams; Global teams; International engineering projects", "domainKnowledge" : "Automotive systems; Manufacturing processes; Real-world simulations; Interactive 3D pipeline; Manufacturing industries; Automotive manufacturing; Process simulation; Product development; Digital transformation; Cloud computing; Generative AI", "domainList" : [ "automotive-systems", "manufacturing-processes", "real-world-simulations", "interactive-3d-pipeline", "manufacturing-industries", "automotive-manufacturing", "process-simulation", "product-development", "digital-transformation", "cloud-computing", "generative-ai" ], "domainSpecificKnowledge" : [ "Automotive systems", "Manufacturing processes", "Real-world simulations", "Interactive 3D pipeline", "Manufacturing industries", "Automotive manufacturing", "Process simulation", "Product development", "Digital transformation", "Cloud computing", "Generative AI" ], "toolProficiency" : [ "NVIDIA Omniverse", "3ds Max", "Maya", "Revit", "Blender", "Substance" ], "continuousLearning" : "Learning opportunities; Global exposure", "innovationCreativity" : "Drive innovation; R&D center", "problemSolvingSkills" : "Problem-solving skills", "qualificationsBasic" : "Proven experience in digital twin development, Proficiency in Python, C#, C++, or Java, Understanding of IoT, data analytics, Hands-on experience with machine learning, Experience with NVIDIA Omniverse, Knowledge of DCC tools, Understanding of full interactive 3D pipeline, Broad technical knowledge across infrastructure, Problem-solving skills, Attention to detail, Communication skills, Ability to work effectively in a team environment, Bachelor’s or Master’s degree", "qualificationsPreferred" : "Experience in automotive manufacturing, Exposure to digital transformation initiatives, Experience developing software solutions across cloud, Knowledge of GPU-based development, Experience working with global teams, Familiarity with advanced visualization tools", "remoteFriendly" : false, "workSiteFlexibility" : "Hybrid", "rawDescription" : "About MBRDI: Mercedes-Benz Research and Development India (MBRDI), headquartered in Bengaluru with a satellite office in Pune, is the largest R&D center for Mercedes-Benz Group AG outside of Germany. Our mission is to drive innovation and excellence in automotive engineering, digitalization, and sustainable mobility solutions, shaping the future of mobility. Key Responsibilities: • Design, develop, and maintain scalable and reliable digital twin models for automotive systems, manufacturing processes, and real-world simulations. • Collaborate with cross-functional engineering, manufacturing, and product teams to integrate digital twins into product development and core manufacturing processes. • Analyze digital twin data to identify actionable insights for optimizing manufacturing processes, improving planning efficiency, and enhancing decision-making. • Develop and demonstrate advanced 3D workflows using NVIDIA Omniverse, including complex 3D pipelines and content creation workflows. • Design and develop software technology architecture tailored to business and client requirements across hybrid cloud and on-premise environments. • Utilize GPUs for developing SDKs and full-stack datacenter architecture to support digital twin and AI-based applications. • Monitor emerging trends and technologies in digital twin development, AI, generative AI, cloud computing, and interactive 3D solutions. Required Skills and Experience: • Proven experience in digital twin development, simulation technologies, or similar AI-driven modeling solutions. • Proficiency in programming languages such as Python, C#, C++, or Java. • Strong understanding of IoT, data analytics, cloud computing, and hybrid cloud environments. • Hands-on experience with machine learning, deep learning, conventional AI, and generative AI technologies. • Experience with NVIDIA Omniverse and 3D content creation workflows. • Knowledge of DCC tools such as 3ds Max, Maya, Revit, Blender, and Substance. • Understanding of the full interactive 3D pipeline, from modeling to application, preferably within manufacturing industries. • Strong passion for manipulating and translating 3D geometry, animation, and materials into code. • Broad technical knowledge across infrastructure requirements, software development, design, and re-engineering. • Strong problem-solving skills, attention to detail, communication skills, and ability to work effectively in a team environment. Educational Qualifications: • Bachelor’s or Master’s degree in Computer Science, Engineering, or a related field. • Additional certifications in AI, Machine Learning, Cloud Computing, Digital Twin, NVIDIA Omniverse, or related technologies would be an added advantage. Preferred Qualifications – Good to Have: • Experience in automotive manufacturing, process simulation, or product development environments. • Exposure to digital transformation initiatives in manufacturing or engineering domains. • Experience in developing software solutions across cloud and on-premise platforms. • Knowledge of GPU-based development, SDK development, and full-stack datacenter architecture. • Experience working with global teams, cross-functional stakeholders, and international engineering projects. • Familiarity with advanced visualization, 3D simulation, and manufacturing process optimization tools. Why Join Us? • Be part of a purpose-driven organization that’s shaping the future of mobility. • Work on cutting-edge technologies such as Digital Twin, AI, Generative AI, NVIDIA Omniverse, and advanced 3D simulations. • Contribute to global automotive engineering and manufacturing transformation projects. • Thrive in a collaborative, diverse, and inclusive environment. • Access world-class infrastructure, learning opportunities, and global exposure. Equal Opportunity Statement: At MBRDI, we are committed to diversity and inclusion. We welcome applications from all qualified individuals, regardless of gender, background, or ability Mercedes-Benz Research and Development India Private Limited", "summaryDescription" : "Digital Twin AI at Mercedes-Benz Research and Development India. Skills: Digital Twin, AI, NVIDIA Omniverse, 3D simulation. Design digital twin models. Develop digital twin models", "createdAt" : "2026-06-14T20:44:02.008", "lastUpdated" : "2026-06-16T03:12:43.875", "ingestTimestamp" : "2026-06-14T20:44:02.008", "mongoId" : "6a191e7658b93c861e39f679", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Digital twin development", "Process simulation", "Product development", "SDK development", "Full-stack datacenter architecture", "Digital Twin", "AI", "NVIDIA Omniverse", "3D simulation", "Software development", "Design", "Re-engineering", "Simulation technologies", "AI-driven modeling", "3D workflows", "3D pipelines", "Content creation", "Software technology architecture", "Datacenter architecture", "Automotive systems", "Manufacturing processes", "Real-world simulations", "Interactive 3D pipeline", "Manufacturing industries", "Automotive manufacturing", "Digital transformation", "Cloud computing", "Generative AI", "AI certifications", "Machine Learning certifications", "Cloud Computing certifications", "Digital Twin certifications", "NVIDIA Omniverse certifications", "3ds Max", "Maya", "Revit", "Blender", "Substance" ], "skillCount" : 38, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 0.6666667, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Manufacturing", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c937674d8ee00a09881e3", "title" : "Associate, Government Affairs", "company" : "Oscar Health", "industry" : "Insurance", "salary" : { "min" : 87188.0, "max" : 114434.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "New York, New York, United States", "locations" : [ "New York", "New York", "United States" ], "timestamp" : "2026-06-15T11:54:54.258", "fingerprint" : "e5ce163681195153ef65dde477f18403e5e4fc70e6aaefdbd88b22346cd7eda8", "source" : "greenhouse", "language" : "en", "applyUrl" : "http://www.hioscar.com/careers/7993044?gh_jid=7993044", "externalId" : "7993044", "industryFunction" : { }, "structuredLocations" : [ { "workMode" : "remote" } ], "locationText" : "", "employmentType" : "FULL_TIME", "professionalSkills" : [ "Regulatory analysis", "Policy analysis", "Legislative tracking" ], "hardSkillsList" : [ "Legislative research", "Regulatory research" ], "hardSkills" : [ { "name" : "Legislative research", "level" : "intermediate" }, { "name" : "Regulatory research", "level" : "intermediate" } ], "majorSkills" : "Government affairs, Regulatory guidance, Public policy", "majorSkillsList" : [ "Government affairs", "Regulatory guidance", "Public policy" ], "coreResponsibilities" : "Track legislative and regulatory developments, Draft summaries of high priority items, Communicate client-focused memoranda, Advise of business impact upon passage, Support trade association relationships, Cover legislative and regulatory hearings, Serve as enterprise resource, Identify and track laws, Prepare summaries and analyses, Assist with company implementation, Present to internal audiences, Digest and communicate developments, Support sustainable processes, Deliver multiple assignments, Adhere to deadlines, Manage competing priorities", "teamCollaboration" : "Partner with PRO Counsel; Partner with Government Affairs colleagues; Partner with cross functional business partners", "domainKnowledge" : "Health plan; Managed care; Public policy; Legislative trends; Regulatory trends", "domainList" : [ "health-plan", "managed-care", "public-policy", "legislative-trends", "regulatory-trends" ], "domainSpecificKnowledge" : [ "Health plan", "Managed care", "Public policy", "Legislative trends", "Regulatory trends" ], "toolProficiency" : [ "Westlaw", "Google Workspace" ], "communicationSkills" : "Client-focused memoranda; Internal presentations", "documentationSkills" : "Draft summaries; Prepare analyses", "qualificationsBasic" : "Bachelor's degree or experience, 3+ years legal/regulatory experience, 2+ years state political/legislative experience, 2+ years Westlaw/tracking software experience", "qualificationsPreferred" : "Familiarity with Affordable Care Act", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Hi, we're Oscar. We're hiring an Associate, Government Affairs to join our Government Affairs. Oscar is the first health insurance company built around a full stack technology platform and a relentless focus on serving our members. We started Oscar in 2012 to create the kind of health insurance company we would want for ourselves—one that behaves like a doctor in the family. About the role: The Associate, Government Affairs, is a major contributor and owner of mission critical workflows to communicate proposed and enacted legislation, regulations, bulletins, and other regulatory guidance to impacted business units. In assigned jurisdictions, the Associate, Government Affairs will track legislative and regulatory developments, draft summaries of high priority items, and communicate client-focused memoranda to Oscar’s compliance team advising of business impact upon passage. The Associate, Government Affairs supports the Government Affairs Counsel in trade association relationships, cover pertinent legislative and regulatory hearings and meetings as assigned, and supports the Government Affairs function by serving as an enterprise wide resource on public policy and legislative and regulatory trends. You will report into the Manager of Government and Regulatory Affairs. Work Location: This position is remote in Washington D. C. #LI-Remote Pay Transparency: The base pay for this role is: $87,188.40 - $114,434.78 per year. You are also eligible for employee benefits, participation in Oscar's unlimited vacation program and annual performance bonuses. Responsibilities: Serve as the subject matter expert on assigned state policy and legislative matters, while identifying and tracking newly proposed and effective laws and regulations in assigned jurisdictions. With support from Government Affairs Counsel, prepare clear, concise, user friendly summaries and analyses based upon client needs of newly effective laws and regulations and assist with company implementation. Present to internal audiences in appropriate forums on priority legislative and regulatory policy developments. Partner with PRO Counsel, Government Affairs colleagues, and cross functional business partners to clearly digest and communicate legislative, regulatory and subregulatory developments. Support sustainable processes which simplify our growing team’s outputs while ensuring high quality deliverables. Deliver multiple, simultaneous and diverse assignments while adhering to deadlines and managing competing priorities in a fast-paced environment. Requirements: Bachelor’s degree in legal studies, political science, public policy, public administration, public health or other relevant field, or a combination of education and experience. 3+ years of legal or regulatory experience, ideally in the health plan/managed care space. 2+ years experience working with state political and legislative processes. 2+ years experience in Westlaw, legislative tracking software, and Google Workspace. Bonus points: Familiarity with the Affordable Care Act and Healthcare.gov or other State Based Exchanges. Experience with Oscar markets. Experience working with attorneys and internal stakeholders. This is an authentic Oscar Health job opportunity. Learn more about how you can safeguard yourself from recruitment fraud here. At Oscar, being an Equal Opportunity Employer means more than upholding discrimination-free hiring practices. It means that we cultivate an environment where people can be their most authentic selves and find both belonging and support. We're on a mission to change health care -- an experience made whole by our unique backgrounds and perspectives. Pay Transparency: Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education, and experience. Full-time employees are eligible for benefits including: medical, dental, and vision benefits, 11 paid holidays, paid sick time, paid parental leave, 401(k) plan participation, life and disability insurance, and paid wellness time and reimbursements. Artificial Intelligence (AI): Our AI Guidelines outline the acceptable use of artificial intelligence for candidates and detail how we use AI to support our recruiting efforts. Reasonable Accommodation: Oscar applicants are considered solely based on their qualifications, without regard to applicant’s disability or need for accommodation. Any Oscar applicant who requires reasonable accommodations during the application process should contact the Oscar Benefits Team (accommodations@hioscar.com) to make the need for an accommodation known. California Residents: For information about our collection, use, and disclosure of applicants’ personal information as well as applicants’ rights over their personal information, please see our Privacy Policy.", "summaryDescription" : "Associate, Government Affairs at Oscar Health. Skills: Government affairs, Regulatory guidance, Public policy. Track legislative and regulatory developments. Draft summaries of high priority items", "postedDate" : "2026-06-14T03:24:13.232", "createdAt" : "2026-06-14T03:24:13.232", "lastUpdated" : "2026-06-15T11:54:54.258", "ingestTimestamp" : "2026-06-14T03:24:13.232", "mongoId" : "6a2c937674d8ee00a09881e3", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 87188, "salaryAnnualMax" : 114434, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Legislative research", "Regulatory research", "Government affairs", "Regulatory guidance", "Public policy", "Regulatory analysis", "Policy analysis", "Legislative tracking", "Health plan", "Managed care", "Legislative trends", "Regulatory trends", "Westlaw", "Google Workspace" ], "skillCount" : 14, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Junior", "dataQualityScore" : 0.8888889, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a19719858b93c861e516d26", "title" : "Digital Twin AI", "company" : "Mercedes-Benz Research and Development India", "industry" : "Manufacturing", "salary" : { "min" : 1850000.0, "max" : 2750000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Digital Twin AI role in Bangalore, India, adjusted for the technology industry and a large company size." }, "location" : "India-Karnataka-Bangalore", "locations" : [ "India-Karnataka-Bangalore", "'Embassy Crest' Plot No 5, , EPIP Zone, Phase 1, " ], "certifications" : [ "AI certifications", "Machine Learning certifications", "Cloud Computing certifications", "Digital Twin certifications", "NVIDIA Omniverse certifications" ], "timestamp" : "2026-06-15T22:32:39.340", "fingerprint" : "8bce43e5980fc2e2568d2665c756dffa59da43c95f7d3bcb17339199b6e05612", "source" : "taleo", "language" : "en", "applyUrl" : "https://daimler.taleo.net/careersection/ex/jobdetail.ftl?job=897846", "externalId" : "897846", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Bangalore", "state" : "Karnataka", "country" : "India", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "12.9767936,77.5900820" } ], "locationText" : "Bangalore, Karnataka, India", "minimumEducation" : "Bachelor's", "technicalSkills" : "Python, C#, C++, Java, IoT, Data analytics, Cloud computing, Hybrid cloud, Machine learning, Deep learning, Generative AI, NVIDIA Omniverse, 3D content creation, 3ds Max, Maya, Revit, Blender, Substance, 3D geometry, Animation, Materials, GPU", "professionalSkills" : [ "Software development", "Design", "Re-engineering", "Simulation technologies", "AI-driven modeling" ], "hardSkillsList" : [ "Digital twin development", "3D workflows", "Datacenter architecture", "SDK development" ], "hardSkills" : [ { "name" : "Digital twin development", "level" : "intermediate" }, { "name" : "3D workflows", "level" : "intermediate" }, { "name" : "Datacenter architecture", "level" : "intermediate" }, { "name" : "SDK development", "level" : "intermediate" } ], "majorSkills" : "Digital Twin, AI, 3D simulations, NVIDIA Omniverse", "majorSkillsList" : [ "Digital Twin", "AI", "3D simulations", "NVIDIA Omniverse" ], "coreResponsibilities" : "Design digital twin models, Develop digital twin models, Maintain digital twin models, Integrate digital twins, Analyze digital twin data, Identify actionable insights, Develop 3D workflows, Demonstrate 3D workflows, Design software technology architecture, Develop software technology architecture, Utilize GPUs for developing SDKs, Develop full-stack datacenter architecture, Monitor emerging trends", "teamCollaboration" : "Cross-functional engineering teams; Manufacturing teams; Product teams; Global teams; Cross-functional stakeholders", "domainKnowledge" : "Automotive systems; Manufacturing processes; Real-world simulations; Interactive 3D pipeline; Automotive manufacturing; Process simulation; Product development; Digital transformation", "domainList" : [ "automotive-systems", "manufacturing-processes", "real-world-simulations", "interactive-3d-pipeline", "automotive-manufacturing", "process-simulation", "product-development", "digital-transformation" ], "domainSpecificKnowledge" : [ "Automotive systems", "Manufacturing processes", "Real-world simulations", "Interactive 3D pipeline", "Automotive manufacturing", "Process simulation", "Product development", "Digital transformation" ], "toolProficiency" : [ "NVIDIA Omniverse", "3ds Max", "Maya", "Revit", "Blender", "Substance" ], "communicationSkills" : "Communication skills", "continuousLearning" : "Learning opportunities", "innovationCreativity" : "Drive innovation", "problemSolvingSkills" : "Problem-solving skills", "outcomesObjectives" : "Optimizing manufacturing processes; Improving planning efficiency; Enhancing decision-making", "qualificationsBasic" : "Proven experience in digital twin development, Proficiency in Python, C#, C++, or Java, Understanding of IoT, data analytics, Hands-on experience with machine learning, Experience with NVIDIA Omniverse, Knowledge of DCC tools, Understanding of full interactive 3D pipeline, Broad technical knowledge across infrastructure, Problem-solving skills, Attention to detail, Communication skills, Ability to work effectively in a team environment, Bachelor’s or Master’s degree", "qualificationsPreferred" : "Experience in automotive manufacturing, Exposure to digital transformation initiatives, Experience developing software solutions across cloud, Knowledge of GPU-based development, Experience working with global teams, Familiarity with advanced visualization tools", "remoteFriendly" : false, "workSiteFlexibility" : "Hybrid", "rawDescription" : "About MBRDI: Mercedes-Benz Research and Development India (MBRDI), headquartered in Bengaluru with a satellite office in Pune, is the largest R&D center for Mercedes-Benz Group AG outside of Germany. Our mission is to drive innovation and excellence in automotive engineering, digitalization, and sustainable mobility solutions, shaping the future of mobility. Key Responsibilities: • Design, develop, and maintain scalable and reliable digital twin models for automotive systems, manufacturing processes, and real-world simulations. • Collaborate with cross-functional engineering, manufacturing, and product teams to integrate digital twins into product development and core manufacturing processes. • Analyze digital twin data to identify actionable insights for optimizing manufacturing processes, improving planning efficiency, and enhancing decision-making. • Develop and demonstrate advanced 3D workflows using NVIDIA Omniverse, including complex 3D pipelines and content creation workflows. • Design and develop software technology architecture tailored to business and client requirements across hybrid cloud and on-premise environments. • Utilize GPUs for developing SDKs and full-stack datacenter architecture to support digital twin and AI-based applications. • Monitor emerging trends and technologies in digital twin development, AI, generative AI, cloud computing, and interactive 3D solutions. Required Skills and Experience: • Proven experience in digital twin development, simulation technologies, or similar AI-driven modeling solutions. • Proficiency in programming languages such as Python, C#, C++, or Java. • Strong understanding of IoT, data analytics, cloud computing, and hybrid cloud environments. • Hands-on experience with machine learning, deep learning, conventional AI, and generative AI technologies. • Experience with NVIDIA Omniverse and 3D content creation workflows. • Knowledge of DCC tools such as 3ds Max, Maya, Revit, Blender, and Substance. • Understanding of the full interactive 3D pipeline, from modeling to application, preferably within manufacturing industries. • Strong passion for manipulating and translating 3D geometry, animation, and materials into code. • Broad technical knowledge across infrastructure requirements, software development, design, and re-engineering. • Strong problem-solving skills, attention to detail, communication skills, and ability to work effectively in a team environment. Educational Qualifications: • Bachelor’s or Master’s degree in Computer Science, Engineering, or a related field. • Additional certifications in AI, Machine Learning, Cloud Computing, Digital Twin, NVIDIA Omniverse, or related technologies would be an added advantage. Preferred Qualifications – Good to Have: • Experience in automotive manufacturing, process simulation, or product development environments. • Exposure to digital transformation initiatives in manufacturing or engineering domains. • Experience in developing software solutions across cloud and on-premise platforms. • Knowledge of GPU-based development, SDK development, and full-stack datacenter architecture. • Experience working with global teams, cross-functional stakeholders, and international engineering projects. • Familiarity with advanced visualization, 3D simulation, and manufacturing process optimization tools. Why Join Us? • Be part of a purpose-driven organization that’s shaping the future of mobility. • Work on cutting-edge technologies such as Digital Twin, AI, Generative AI, NVIDIA Omniverse, and advanced 3D simulations. • Contribute to global automotive engineering and manufacturing transformation projects. • Thrive in a collaborative, diverse, and inclusive environment. • Access world-class infrastructure, learning opportunities, and global exposure. Equal Opportunity Statement: At MBRDI, we are committed to diversity and inclusion. We welcome applications from all qualified individuals, regardless of gender, background, or ability Mercedes-Benz Research and Development India Private Limited", "summaryDescription" : "Digital Twin AI at Mercedes-Benz Research and Development India. Skills: Digital Twin, AI, 3D simulations, NVIDIA Omniverse. Design digital twin models. Develop digital twin models", "createdAt" : "2026-06-14T17:53:44.834", "lastUpdated" : "2026-06-15T22:32:39.340", "ingestTimestamp" : "2026-06-14T17:53:44.834", "mongoId" : "6a19719858b93c861e516d26", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Digital twin development", "3D workflows", "Datacenter architecture", "SDK development", "Digital Twin", "AI", "3D simulations", "NVIDIA Omniverse", "Software development", "Design", "Re-engineering", "Simulation technologies", "AI-driven modeling", "Automotive systems", "Manufacturing processes", "Real-world simulations", "Interactive 3D pipeline", "Automotive manufacturing", "Process simulation", "Product development", "Digital transformation", "AI certifications", "Machine Learning certifications", "Cloud Computing certifications", "Digital Twin certifications", "NVIDIA Omniverse certifications", "3ds Max", "Maya", "Revit", "Blender", "Substance" ], 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"structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 5, "experienceLevel" : "Manager", "professionalSkills" : [ "Regulatory strategy", "Client communication", "Health authority interaction", "Cross-functional project management", "Regulatory dossier preparation", "Regulatory approach design", "Program delivery", "Regulatory documentation", "Quality systems", "Safety reporting processes" ], "hardSkillsList" : [ "Regulatory affairs", "Pharmacovigilance", "Expanded Access Programs", "Biologics", "Synthetic drugs", "Regulatory dossiers", "Global regulations", "SOPs", "CAPAs", "Safety reporting" ], "softSkillsList" : [ "Leadership", "Solution-oriented" ], "hardSkills" : [ { "name" : "Regulatory affairs", "level" : "intermediate" }, { "name" : "Pharmacovigilance", "level" : "intermediate" }, { "name" : "Expanded Access 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SME in health authority interactions, Serve as regulatory SME in audits, Serve as pharmacovigilance SME in audits, Serve as regulatory SME in project meetings, Serve as pharmacovigilance SME in project meetings, Prepare regulatory dossiers for EAPs, Compile regulatory dossiers for EAPs, Submit regulatory dossiers for EAPs, Contribute to regulatory approach design for EAP setup, Contribute to regulatory approach execution for EAP setup, Ensure timely execution of regulatory activities, Ensure accurate execution of regulatory activities, Ensure compliant execution of regulatory activities, Ensure timely execution of pharmacovigilance activities, Ensure accurate execution of pharmacovigilance activities, Ensure compliant execution of pharmacovigilance activities, Collaborate with Medical Affairs, Collaborate with Quality Assurance, Collaborate with Program Management, Collaborate with Supply Chain, Collaborate with Commercial teams, Maintain knowledge of global regulations, Maintain 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experience in Regulatory Affairs, Foundational knowledge of Pharmacovigilance principles, Knowledge of global safety reporting requirements, Understanding of national regulations governing Expanded Access, Understanding of international regulations governing Expanded Access, Bachelor’s or Master’s degree, Experience working with external stakeholders, Excellent written communication skills, Excellent verbal communication skills, Proficiency with Microsoft 365 tools", "qualificationsPreferred" : "Direct exposure to Expanded Access Programs", "remoteFriendly" : true, "workSiteFlexibility" : "Flexible", "rawDescription" : "## Accountabilities Lead and support regulatory strategy development for Expanded Access Programs (EAPs), including programs involving biologics, cell and gene therapies, and synthetic drugs. Serve as a regulatory and pharmacovigilance subject matter expert in client communications, health authority interactions, audits, and cross-functional project meetings. Prepare, compile, and submit complete regulatory dossiers for both cohort-based and named-patient EAPs on behalf of clients. Contribute to the design and execution of regulatory approaches for EAP setup, including geographic and operational considerations. Ensure timely, accurate, and compliant execution of all regulatory and pharmacovigilance activities related to EAP operations. Collaborate closely with Medical Affairs, Quality Assurance, Program Management, Supply Chain, and Commercial teams to ensure seamless program delivery. Maintain up-to-date knowledge of global regulations and guidelines impacting Expanded Access and ensure internal alignment with evolving requirements. Support the development, review, and maintenance of regulatory documentation, templates, SOPs, CAPAs, and quality systems. Liaise with pharmacovigilance service providers to ensure end-to-end compliance and alignment of safety reporting processes. Requirements: Approximately 5 years of experience in Regulatory Affairs, with direct exposure to Expanded Access Programs strongly preferred. Solid foundational knowledge of Pharmacovigilance principles and global safety reporting requirements. Strong understanding of national and international regulations governing Expanded Access and related regulatory frameworks. Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine, or a related scientific discipline. Proven experience working with external stakeholders, including pharmaceutical clients or regulatory authorities. Excellent written and verbal communication skills in English, with the ability to translate complex regulatory concepts into clear guidance. Strong collaboration skills and ability to work effectively in cross-functional, international environments. Proactive, solution-oriented mindset with the ability to anticipate regulatory risks and propose practical solutions. Proficiency with Microsoft 365 tools (Word, Excel, Teams, SharePoint) and comfort working in digital, process-driven environments. Benefits: Competitive salary with annual performance-based bonus Employee Stock Option Plan (ESOP) Learning and development budget and continuous internal knowledge-sharing opportunities Hybrid working flexibility (for eligible regions) and support for work-life balance Policies supporting working parents and caregivers Access to confidential mental health and psychological support services International, mission-driven work environment focused on improving patient access to therapies Regular team events, culture initiatives, and company-wide celebrations Opportunity to contribute directly to impactful work enabling access to potentially life-saving treatments Career growth opportunities within a fast-scaling global organization. ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Regulatory Affairs Pharmacovigilance Manager. Skills: Regulatory Affairs, Pharmacovigilance, Expanded Access Programs. Lead regulatory strategy development for EAPs. 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Pawtucket, Rhode Island, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 10, "experienceLevel" : "Director", "professionalSkills" : [ "Regulatory strategy", "Risk management", "Legal analysis", "Compliance oversight", "Problem-solving" ], "hardSkillsList" : [ "Regulatory affairs", "Promotional material review", "Clinical trial design", "Clinical data interpretation" ], "softSkillsList" : [ "Leadership", "Interpersonal skills" ], "hardSkills" : [ { "name" : "Regulatory affairs", "level" : "intermediate" }, { "name" : "Promotional material review", "level" : "intermediate" }, { "name" : "Clinical trial design", "level" : "intermediate" }, { "name" : "Clinical data interpretation", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Interpersonal skills" } ], "majorSkills" : "Regulatory affairs, Advertising promotion, FDA regulations", "majorSkillsList" : [ "Regulatory affairs", "Advertising promotion", "FDA regulations" ], "coreResponsibilities" : "Provide strategic regulatory advice, Review product promotion materials, Review disease state education materials, Review pipeline materials, Review Medical materials, Provide strategic regulatory support, Generate innovative solutions, Develop internal cross-functional relationships, Monitor regulatory environment, Interpret new regulations, Interpret guidance documents, Interpret enforcement activities, Maintain in-depth understanding, Communicate complex issues, Establish relationship with OPDP, Provide oversight of promotional material review, Ensure on-time submission, Ensure accurate submission, Assist with training employees, Develop process efficiencies, Improve process efficiencies, Act in accordance with Company policies, Ensure policies are understood, Ensure policies are followed", "teamCollaboration" : "Cross-functional relationships; Commercial team; Medical Affairs team; Legal team; Compliance team; Corporate Affairs team; Development team", "domainKnowledge" : "Biopharmaceutical industry; Neuroscience; Ion channel biology; FDA regulations; Prescription drug promotion", "domainList" : [ "biopharmaceutical-industry", "neuroscience", "ion-channel-biology", "fda-regulations", "prescription-drug-promotion" ], "domainSpecificKnowledge" : [ "Biopharmaceutical industry", "Neuroscience", "Ion channel biology", "FDA regulations", "Prescription drug promotion" ], "communicationSkills" : "Verbal communication; Written communication; Interpersonal communication; Listening skills; Clear communication; Concise communication", "documentationSkills" : "Regulatory filings", "continuousLearning" : "Training; Learning and Development program; Tuition Assistance program", "problemSolvingSkills" : "Effective problem-solving", "outcomesObjectives" : "Meet goals and objectives", "qualificationsBasic" : "Bachelor's degree, 10+ years experience, 8+ years Advertising Promotion, FDA laws regulations guidances, Manage complex matrixed environment", "qualificationsPreferred" : "Advanced degree preferred", "remoteFriendly" : false, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Who We Are: Xenon Pharmaceuticals (NASDAQ:XENE https://www.nasdaq.com/market-activity/stocks/xene) is a neuroscience-focused biopharmaceutical company dedicated to drug discovery, clinical development, and commercialization of life-changing therapeutics for patients in need. We are looking for great people who thrive in a respectful, collaborative, inclusive, and productive culture to join the Xenon team. What We Do: We are advancing an exciting product pipeline https://xenon-pharma.com/pipeline to address indications with high unmet medical need, including epilepsy, depression and pain. Our Phase 3 azetukalner program represents the most advanced, clinically validated potassium channel modulator in late-stage clinical development for multiple indications. In March 2026, we announced positive topline data from our Phase 3 X-TOLE2 study of azetukalner in focal onset seizures (FOS), and we anticipate submitting a New Drug Application to the Food and Drug Administration in the third quarter of 2026. Our Phase 3 epilepsy program also includes a second FOS study, X-TOLE3, which would support regulatory submissions outside the U.S., and the X-ACKT study in primary generalized tonic-clonic seizures, which would support regulatory submissions for an additional epilepsy indication. We also have multiple Phase 3 azetukalner clinical trials underway in major depressive disorder (MDD) and bipolar depression (BPD), based on topline data from our Phase 2 X-NOVA clinical trial. In addition, we are proud of our strong heritage in human genetics, deep understanding of ion channel biology, and expertise in novel chemistries to enable potent, selective ion channel targeting. We continue to advance an early-stage pipeline of novel therapeutic candidates, including Phase 1 studies for XEN1701 (targeting Nav1.7) and XEN1120 (targeting Kv7), which are important pain targets. Backed by a strong balance sheet to support our growth plans, we continue to build a fully integrated, premier neuroscience company with strong discovery, clinical development, corporate, and commercial operations. About the Role: We are seeking a Director, Regulatory affairs, Commercial (Advertising & Promotion), to join our Regulatory Affairs team. The Director will be responsible for strategic regulatory advice and direction for marketed products and development compounds in alignment with the overarching regulatory and brand strategy. The Director will have oversight of day-to-day activities for their assigned role, department activities, and direct reports (if applicable) in order to meet goals and objectives. The Director will report to the VP of Commercial Regulatory Affairs. This position reports to the Vice President, Regulatory Affairs, Commercial and will be based out of Boston, MA, USA in our Needham office. This is a Hybrid position requiring a minimum of two onsite days per week. RESPONSIBILITIES: - Provide strategic regulatory advice, review, and decisions for product promotion, disease state education, pipeline, and Medical materials for alignment with applicable FDA regulations and guidance documents - Provide strategic regulatory support to the business by generating innovative solutions and effective problem-solving aligned with the company’s guiding principles in order to achieve desired outcomes - Develop and establish strong internal cross-functional relationships with the Commercial, Medical Affairs, Legal, Compliance, Corporate Affairs, and Development to foster open communication, collaboration, and teamwork - Continually monitors and evaluates the regulatory environment, interprets new regulations, guidance documents, enforcement activities and trends for potential impact on the business and company - Maintain in-depth understanding of clinical trial design and interpretation of clinical data and communicate complex issues clearly and concisely - Establishes and maintains a relationship with the Office of Prescription Drug Promotion (OPDP) at FDA - Provide appropriate oversight of promotional material review and ensure on-time and accurate submission of applicable materials to FDA - Assist with training employees at Xenon and in developing and improving process efficiencies - Act in accordance with Company policies, including, for example, the Code of Business Conduct and Ethics and ensure policies are understood and followed by direct reports, if any - Other duties as assigned QUALIFICATIONS: - At minimum, a relevant four-year undergraduate degree; An advanced degree is preferred - 10+ years of experience in progressive Regulatory Affairs management positions in the biotech or pharmaceutical industry; A minimum of 8 years of experience focused on Regulatory Advertising and Promotion - Strong verbal and written communication skills; interpersonal and listening skills implemented in a positive and effective manner - Expertise in applicable FDA laws, regulations, guidances, and industry standards - Ability to manage a complex matrixed environment with multiple competing priorities and tasks appropriately and with autonomy - Strong communication, leadership and interpersonal skills required 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, Regulatory Affairs, Commercial (Advertising & Promotion) at Xenon Pharmaceuticals. Skills: Regulatory affairs, Advertising promotion, FDA regulations. Provide strategic regulatory advice. 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Program Management; Medical Affairs; Quality Assurance; Supply Chain", "projectManagementSkills" : [ "Program management" ], "domainKnowledge" : "Expanded Access Programs; Clinical trials; Real-World Data", "domainList" : [ "expanded-access-programs", "clinical-trials", "real-world-data" ], "domainSpecificKnowledge" : [ "Expanded Access Programs", "Clinical trials", "Real-World Data" ], "communicationSkills" : "Stakeholder management", "qualificationsBasic" : "Significant experience in Regulatory Affairs, Experience in pharma, biotech, or CRO, Proven experience managing multiple programs, Proven experience managing complex regulatory portfolios, Knowledge of global regulatory frameworks, Demonstrated leadership experience managing teams, Demonstrated experience developing talent", "remoteFriendly" : true, "rawDescription" : "About myTomorrows myTomorrows is a global health tech company dedicated to breaking down barriers for patients seeking treatment options.    We strive to enable earlier and better treatment access by bridging the gap between those searching for possible options, and the companies who develop them. We work closely with patients, healthcare professionals, trial sites, patient advocacy groups, and BioPharma – connecting key stakeholders in the drug development ecosystem.    We’ve developed a cutting-edge AI-powered technology platform that simplifies and streamlines access to drugs in development. To support our users and clients, we have a range of industry-expert specialized teams ready to help. Our services include clinical trial patient recruitment, Expanded Access Program management and Real-World Data collection.    With a global footprint spanning 134 countries, to date we’ve supported over 17,000 patients, 3,000 physicians and 350 sites, earning the trust of 60+ BioPharma companies. In October 2025, we closed a €25M investment with Avego Healthcare Capital to fuel our global ambitions and scale the business.   Join us in shaping the future of treatment access - making tomorrow’s therapies accessible for people who need them today. THE OPPORTUNITY: REGULATORY AFFAIRS DIRECTOR As Regulatory Affairs Director, you will play a critical leadership role in translating our global regulatory strategy into execution across programs, regions, and service lines. You will oversee a portfolio of regulatory activities, ensuring high-quality, compliant, and timely delivery while leading and developing a team of Regulatory Affairs professionals. You’ll work closely with cross-functional teams and act as a senior point of contact for both internal stakeholders and external partners. This role sits at the intersection of strategy, delivery, and leadership, and is key to scaling our Regulatory Affairs capabilities globally. WHAT YOU'LL DO IN THIS ROLE: DRIVE REGULATORY STRATEGY EXECUTION - Translate company and RA/PV strategy into clear regulatory plans across programs and regions - Drive implementation across Expanded Access Programs (EAPs), Clinical Trials, and Real-World Data initiatives OVERSEE PROGRAM AND PORTFOLIO DELIVERY - Oversee multiple regulatory programs simultaneously, ensuring delivery against timelines, quality standards, and client expectations - Identify and proactively manage cross-program risks, dependencies, and resource constraints LEAD AND DEVELOP THE TEAM - Lead, coach, and develop Regulatory Affairs Managers and senior team members - Set clear expectations and drive accountability for performance, quality, and delivery COLLABORATE CROSS-FUNCTIONALLY - Partner closely with Program Management, Medical Affairs, Quality Assurance, and Supply Chain - Ensure regulatory input is embedded into end-to-end program delivery DRIVE OPERATIONAL EXCELLENCE AND PERFORMANCE - Drive standardization, consistency, and scalability of regulatory processes - Identify improvement opportunities and implement data-driven solutions ENGAGE WITH CLIENTS AND STAKEHOLDERS - Act as a senior point of contact for clients on regulatory matters - Support client discussions, audits, and regulatory interactions with Health Authorities ENSURE QUALITY, COMPLIANCE, AND RISK MANAGEMENT - Ensure adherence to global regulatory requirements and internal processes - Support inspection readiness and audit preparedness WHAT YOU BRING TO THE TABLE: - Advanced degree in life sciences, pharmacy, or a related field - Significant experience in Regulatory Affairs within pharma, biotech, or CRO environments - Proven experience managing multiple programs and complex regulatory portfolios - Strong knowledge of global regulatory frameworks (EAP, clinical trials, or similar environments) - Demonstrated leadership experience managing teams and developing talent - Excellent stakeholder management and communication skills Equal opportunities myTomorrows is an Equal Opportunity Employer and, beyond upholding discrimination-free practices, we are committed to cultivating a workplace where difference and diversity are protected and celebrated. The best work comes from our best selves, and we go to great lengths in supporting our team members to be just that. ", "summaryDescription" : "Regulatory Affairs Director at myTomorrows. Translate company and RA/PV strategy into regulatory plans. Drive implementation across EAPs", "postedDate" : "2026-06-11T16:58:12.288", "createdAt" : "2026-06-11T16:58:12.288", "lastUpdated" : "2026-06-13T08:55:22.340", "ingestTimestamp" : "2026-06-11T16:58:12.288", "mongoId" : "6a2a7bcf74d8ee00a06646d4", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "Regulatory affairs", "Global regulatory frameworks", "EAP", "Clinical trials", "Real-world data", "Leadership", "Regulatory strategy", "Program delivery", "Portfolio management", "Risk management", "Quality assurance", "Client engagement", "Program management", "Expanded Access Programs", "Real-World Data" ], "skillCount" : 15, "jobCategory" : "operations", "jobSubcategory" : "regulatory-affairs-and-pharmacovigilance-management", "dataQualityScore" : 1.0, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Health Tech" }, { "id" : "6a2cc30874d8ee00a0a0828e", "title" : "Senior Staff Research Scientist, Speech Technologies", "company" : "Hippocratic AI", "industry" : "Product and Engineering", "salary" : { "min" : 350000.0, "max" : 550000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Senior Staff Research Scientist, Speech Technologies in Bellevue, United States, adjusted for executive seniority and the healthcare industry." }, "location" : "Bellevue, WA", "locations" : [ "Bellevue, WA" ], "timestamp" : "2026-06-15T08:17:16.565", "fingerprint" : "eaa0560dc4f1421cc9e890465d81bf191ea9979e60a29e103a76ff0981c3216a", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/hippocratic%20ai/8154a8c9-8204-464c-9b39-88a75e0201d6/application", "externalId" : "8154a8c9-8204-464c-9b39-88a75e0201d6", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Bellevue", "state" : "Washington", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "47.6144219,-122.1923370" } ], "locationText" : "Bellevue, Washington, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Speech recognition, ASR models, Python, C++, LLMs", "professionalSkills" : [ "Research engineering", "Data infrastructure", "Model validation", "Resource efficiency" ], "hardSkillsList" : [ "Streaming speech recognition", "Non-streaming speech recognition", "End-to-end architectures", "Model optimization", "Dataset curation", "GPU-accelerated training", "Inference" ], "softSkillsList" : [ "Clear communicator" ], "hardSkills" : [ { "name" : "Streaming speech recognition", "level" : "intermediate" }, { "name" : "Non-streaming speech recognition", "level" : "intermediate" }, { "name" : "End-to-end architectures", "level" : "intermediate" }, { "name" : "Model optimization", "level" : "intermediate" }, { "name" : "Dataset curation", "level" : "intermediate" }, { "name" : "GPU-accelerated training", "level" : "intermediate" }, { "name" : "Inference", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Clear communicator" } ], "majorSkills" : "ASR foundation, Speech recognition, Data pipelines", "majorSkillsList" : [ "ASR foundation", "Speech recognition", "Data pipelines" ], "coreResponsibilities" : "Design ASR models, Develop ASR models, Iterate on ASR models, Research end-to-end architectures, Implement end-to-end architectures, Train ASR models, Evaluate ASR models, Optimize ASR models, Preprocess speech datasets, Curate speech datasets, Collaborate with LLM teams, Collaborate with product teams, Collaborate with clinical teams, Integrate speech technologies, Contribute to research culture, Experimentation, Documentation, Knowledge sharing", "teamCollaboration" : "Cross-functional partners; LLM teams; Product teams; Clinical teams", "domainKnowledge" : "Medical terminology; Clinical accuracy; Healthcare LLM; Conversational AI; Medical speech datasets", "domainList" : [ "medical-terminology", "clinical-accuracy", "healthcare-llm", "conversational-ai", "medical-speech-datasets" ], "domainSpecificKnowledge" : [ "Medical terminology", "Clinical accuracy", "Healthcare LLM", "Conversational AI", "Medical speech datasets" ], "toolProficiency" : [ "ESPnet", "Kaldi", "PyTorch", "CUDA" ], "communicationSkills" : "Translate technical work", "documentationSkills" : "Documentation", "innovationCreativity" : "Research culture", "problemSolvingSkills" : "Solve speech recognition problems", "specialRequirements" : "Quarterly trips to Menlo Park", "qualificationsBasic" : "PhD with 7+ years ASR research, Master's with 10+ years speech recognition, Designing algorithms for speech recognition, Training and optimizing ASR models, Preprocessing and curating speech datasets, Python and C++ programming, Linux/Unix command-line environments", "qualificationsPreferred" : "Building ASR systems from 0 to 1, Practical experience with ESPnet, Practical experience with Kaldi, Practical experience with PyTorch, Experience with CUDA, Familiarity with leveraging LLMs, Experience with neural endpointer modeling, Experience with end-to-end endpointer modeling, Publications in tier-1 venues", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "THE OPPORTUNITY Healthcare has a access problem — not enough clinicians, too many patients, and critical gaps that technology hasn't meaningfully closed. Hippocratic AI is changing that. Our safety-focused, healthcare-only LLM platform enables autonomous, clinical-grade conversations with patients at a scale no human workforce could achieve. With over $404M in funding, a $3.5B valuation, and partnerships with leading health systems, we're not iterating on existing tools — we're building a new category. At the center of that platform is voice. As a Senior Staff Research Scientist in Speech Technologies, you'll lead the research and engineering that makes our AI not just intelligent, but genuinely conversational — accurate, fast, and trustworthy in the highest-stakes environments imaginable. WHAT YOU'LL ACCOMPLISH - You'll define the ASR foundation for healthcare's most advanced conversational AI. From architecture selection to production deployment, you'll shape a speech recognition system built from the ground up for clinical accuracy — one that sets the standard for what's possible when safety and performance aren't trade-offs. - You'll solve speech recognition problems that don't have off-the-shelf answers. Medical terminology, diverse patient populations, real-world acoustic conditions — you'll design and validate models that perform where general-purpose ASR falls short, pushing the frontier of what conversational AI can reliably understand. - You'll build the data infrastructure that makes breakthrough models possible. You'll architect the pipelines and curation processes for large-scale medical speech datasets, creating the training foundation that gives Hippocratic AI a durable, compounding advantage in clinical speech recognition. - You'll bring research into the real world at meaningful scale. You'll close the gap between state-of-the-art methods and production systems — optimizing for latency, accuracy, and resource efficiency so that patients and clinicians experience the results of your work in every conversation. LOCATION REQUIREMENTS We believe the best ideas happen together. We're on the hunt for a great space in the Bellevue area — and when we find it, this role will be in office five days a week. In the meantime, you'll work fully remote with quarterly trips to our Menlo Park, CA headquarters to connect and collaborate with the team. RESPONSIBILITIES - Design, develop, and iterate on data-driven ASR models for streaming and non-streaming conversational speech applications - Research and implement state-of-the-art end-to-end speech recognition architectures tailored to the medical domain - Train, evaluate, and optimize ASR models across accuracy, latency, and resource utilization dimensions - Preprocess and curate large-scale speech datasets to support robust model training - Collaborate closely with LLM, product, and clinical teams to integrate speech technologies into the broader Hippocratic AI platform - Contribute to the team's research culture through experimentation, documentation, and knowledge sharing BASIC QUALIFICATIONS - PhD with 7+ years of hands-on ASR research and engineering experience, or a Master's degree with 10+ years of industry experience in speech recognition - Deep experience designing and developing algorithms for accurate, efficient speech recognition in both streaming and non-streaming contexts - Proven track record training and optimizing ASR models for production — balancing accuracy, latency, and compute constraints - Experience preprocessing and curating large speech datasets for model training - Strong Python and C++ programming skills - Comfortable working in Linux/Unix command-line environments - Clear communicator — you can translate complex technical work for cross-functional partners PREFERRED QUALIFICATIONS - Hands-on experience building ASR systems from 0 to 1, including data pipelines, model architecture selection, and evaluation frameworks - Practical experience with ESPnet, Kaldi, and PyTorch - Experience with CUDA for GPU-accelerated training and inference - Familiarity with leveraging LLMs to enhance speech recognition quality - Experience with neural and end-to-end endpointer modeling - Publications in tier-1 venues in speech recognition or NLP (Interspeech, ICASSP, ACL, etc.) WHAT YOU'LL LOVE ABOUT HIPPOCRATIC AI - The mission is real. Every improvement you make to speech recognition translates directly into better patient experiences — more accurate conversations, fewer errors, broader access to care for people who currently have none. - The team is exceptional. You'll work alongside researchers and engineers from Google, Meta, Microsoft, NVIDIA, and Stanford, as well as clinicians and health system leaders who keep the work grounded in what actually matters to patients. - The technical problems are genuinely hard. This isn't fine-tuning an existing API. It's building a purpose-built, safety-critical speech stack for one of the most complex and consequential domains in the world. - The strategic moment is now. With $404M raised, a $3.5B valuation, and real deployments across leading health systems, Hippocratic AI has both the resources and the momentum to define this category — and the equity upside to match. --- READY TO APPLY? If you've spent your career pushing what speech recognition can do and you want that work to matter in ways that reach millions of patients — we'd like to talk. Apply with your resume and, if you have relevant publications or projects you're proud of, share those too. We review every application and move quickly with candidates who are a strong fit.", "summaryDescription" : "Senior Staff Research Scientist, Speech Technologies at Hippocratic AI. Skills: ASR foundation, Speech recognition, Data pipelines. Design ASR models. Develop ASR models", "createdAt" : "2026-06-13T22:01:25.207", "lastUpdated" : "2026-06-15T08:17:16.565", "ingestTimestamp" : "2026-06-13T22:01:25.207", "mongoId" : "6a2cc30874d8ee00a0a0828e", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 350000, "salaryAnnualMax" : 550000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Streaming speech recognition", "Non-streaming speech recognition", "End-to-end architectures", "Model optimization", "Dataset curation", "GPU-accelerated training", "Inference", "Clear communicator", "ASR foundation", "Speech recognition", "Data pipelines", "Research engineering", "Data infrastructure", "Model validation", "Resource efficiency", "Medical terminology", "Clinical accuracy", "Healthcare LLM", "Conversational AI", "Medical speech datasets", "ESPnet", "Kaldi", "PyTorch", "CUDA" ], "skillCount" : 24, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Executive", "dataQualityScore" : 0.8888889, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2c6af174d8ee00a090f510", "title" : "Digital Designer (AI & Figma)", "company" : "Bybit", "industry" : "FinTech", "salary" : { "min" : 60000.0, "max" : 90000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Digital Designer in Bulgaria, adjusted for the FinTech industry and remote work." }, "location" : "Remote General (Non-EU)", "locations" : [ "Remote General (Non-EU)" ], "timestamp" : "2026-06-16T00:15:17.189", "fingerprint" : "d4fa4b68df8e5b52a19feba9f85244f0883664fbd485a9ef6dae886d32a85148", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.eu.greenhouse.io/bybit/jobs/4870590101", "externalId" : "4870590101", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Bulgaria", "continent" : "eu", "workMode" : "remote" } ], "locationText" : "Bulgaria", "employmentType" : "CONTRACT", "experienceMinYears" : 3, "experienceMaxYears" : 5, "experienceLevel" : "Mid-level", "technicalSkills" : "Figma, AI", "professionalSkills" : [ "Task management", "Creative thinking", "Technical execution" ], "hardSkillsList" : [ "Graphic design", "Visual creation", "Print production", "File preparation" ], "hardSkills" : [ { "name" : "Graphic design", "level" : "intermediate" }, { "name" : "Visual creation", "level" : "intermediate" }, { "name" : "Print production", "level" : "intermediate" }, { "name" : "File preparation", "level" : "intermediate" } ], "coreResponsibilities" : "Create visual assets, Develop AI-generated graphics, Build design systems, Manage Figma components, Maintain Figma libraries, Collaborate with teams, Deliver creative solutions, Prepare files for print", "teamCollaboration" : "Internal teams", "domainKnowledge" : "Digital finance; Cryptocurrency exchange; Web3", "domainList" : [ "digital-finance", "cryptocurrency-exchange", "web3" ], "domainSpecificKnowledge" : [ "Digital finance", "Cryptocurrency exchange", "Web3" ], "toolProficiency" : [ "Figma", "AI tools" ], "continuousLearning" : "Study Growth Fund", "innovationCreativity" : "AI tools", "qualificationsBasic" : "3-5 years graphic design, Proficiency in English, Advanced AI tools experience, High proficiency in Figma", "qualificationsPreferred" : "Knowledge of print production, Experience in crypto/Web3, Experience in fintech, Experience in neo-banking, Experience with marketing creative, Experience with performance creative, Familiarity with motion design, Familiarity with video editing", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "About Us Established in 2018, Bybit is one of the world’s leading cryptocurrency exchanges and digital financial platforms, serving over 80 million users across more than 200 countries and regions. Powered by world-class technology and a user-first mindset, Bybit delivers a seamless ecosystem across trading, payments, wealth management, custody, institutional services, and Web3 — connecting users to the future of digital finance. Our core values define how we build. We listen, care and improve to create products and experiences that put users first. Backed by a global team of ambitious builders, problem-solvers, and innovators, we foster a high-performance and fast-moving environment where talent is empowered to drive real impact at the global scale. Supported by 24/7 multilingual customer service and a strong commitment to innovation, we are shaping the future of finance through technology, collaboration, and bold execution. Today, Bybit is recognized as one of the most trusted and transparent platforms in the digital asset industry, continuing to expand its global presence while building the infrastructure for the next generation of financial services. Digital Designer Location: Remote (Freelance) Experience Level: Mid-level (3–5 years) About the Role We are looking for a freelance mid-level graphic designer to support ongoing creative needs across digital and print channels. This role requires a strong balance between creative thinking and technical execution, with a particular focus on leveraging AI tools to generate high-quality visuals and scalable design assets. The ideal candidate is highly autonomous, with a strong sense of ownership and task management, and is comfortable working in a fast-paced environment with tight deadlines. Key Responsibilities Create high-quality visual assets for digital campaigns, social media, and marketing materials Develop AI-generated graphics and visuals, including 3D, lifestyle and illustrations Work within and expand existing design systems and libraries using Figma Build, manage, and maintain components and libraries in Figma Collaborate with internal teams to deliver creative solutions aligned with brand guidelines Prepare files for print production when required Ensure consistency and quality across all deliverables Required Skills & Qualifications 3–5 years of experience in graphic design (agency or in-house) Strong proficiency in written and spoken English Advanced experience using AI tools for visual creation High proficiency in Figma, including: Components and variants Design systems management Plugin usage and workflow optimization Strong understanding of layout, typography, and visual hierarchy Ability to work independently and manage deadlines in a freelance setup Nice to Have Knowledge of print production and file preparation Experience in crypto/Web3, exchanges, fintech, neo-banking, or similar industries Experience working with marketing or performance-driven creative Familiarity with motion design or Video editing Why Join Us At Bybit, we are committed to fostering a supportive and enriching work environment. Our benefits include: - Study Growth Fund: We support your professional development and continuous learning. - Internal Events: Participate in regular team-building activities, workshops, and events designed to promote collaboration and innovation. - Global Collaboration: Be part of a diverse, international team, working alongside colleagues from around the world. - Career Advancement: Access opportunities for growth and advancement within a rapidly expanding global company. - Internal Mobility: Grow with us- Your long-term development is important to us. We offer internal job opportunities to help build your career path.", "summaryDescription" : "Digital Designer (AI & Figma) at Bybit. Create visual assets. Develop AI-generated graphics", "postedDate" : "2026-06-14T20:06:39.525", "createdAt" : "2026-06-14T20:06:39.525", "lastUpdated" : "2026-06-16T00:15:17.189", "ingestTimestamp" : "2026-06-14T20:06:39.525", "mongoId" : "6a2c6af174d8ee00a090f510", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "50k-75k", "hasSalary" : false, "allSkills" : [ "Graphic design", "Visual creation", "Print production", "File preparation", "Task management", "Creative thinking", "Technical execution", "Digital finance", "Cryptocurrency exchange", "Web3", "Figma", "AI tools" ], "skillCount" : 12, "jobCategory" : "product", "jobSubcategory" : "design", "seniorityLevel" : "Mid", "dataQualityScore" : 1.0, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "FinTech", "llmIndustryConfidence" : 0.98 }, { "id" : "6a30511af292fd229cefa70e", "title" : "Staff AI Execution Engineer", "industry" : "IT", "salary" : { "min" : 200000.0, "max" : 220000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "US", "locations" : [ "US" ], "timestamp" : "2026-06-16T12:33:21.952", "fingerprint" : "ec92f56b7428371f7b0ad40951f92f52337309cba90735446e1d3786c2ca76fd", "source" : "lever", "language" : "en", "applyUrl" : "https://jobs.lever.co/jobgether/77cefa92-09a4-42be-8617-17667fc2502b/apply", "externalId" : "77cefa92-09a4-42be-8617-17667fc2502b", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Bulgaria", "continent" : "eu", "workMode" : "remote" } ], "locationText" : "Bulgaria", "employmentType" : "FULL_TIME", "experienceMinYears" : 8, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "AI, Machine learning, Agent orchestration, Memory systems, Evaluation frameworks, Distributed systems, LangChain, LangGraph, GraphQL, MCP, Cursor, Claude Code, Devin, SQL, Python, Snowflake, Dbt, Kafka, CDC pipelines, APIs", "professionalSkills" : [ "System design", "AI system design", "Delivery management" ], "hardSkillsList" : [ "Prompt design", "Multi-agent orchestration", "Context optimization", "Data engineering", "Data analysis", "Performance measurement" ], "softSkillsList" : [ "Leadership", "Communication skills" ], "hardSkills" : [ { "name" : "Prompt design", "level" : "intermediate" }, { "name" : "Multi-agent orchestration", "level" : "intermediate" }, { "name" : "Context optimization", "level" : "intermediate" }, { "name" : "Data engineering", "level" : "intermediate" }, { "name" : "Data analysis", "level" : "intermediate" }, { "name" : "Performance measurement", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Communication skills" } ], "majorSkills" : "AI Execution, Agentic AI, Production systems", "majorSkillsList" : [ "AI Execution", "Agentic AI", "Production systems" ], "coreResponsibilities" : "Design production-grade AI systems, Build production-grade AI systems, Deploy production-grade AI systems, Own end-to-end AI delivery, Deliver agent orchestration, Deliver memory systems, Deliver evaluation frameworks, Deliver production hardening, Architect scalable AI workflows, Ensure reliability, Ensure observability, Ensure performance, Develop evaluation frameworks, Implement evaluation frameworks, Measure agent behavior, Improve agent behavior, Optimize agent behavior, Leverage agentic AI tools, Leverage agentic AI frameworks, Accelerate development velocity, Improve engineering productivity, Drive AI-native best practices, Drive prompt design, Drive multi-agent orchestration, Drive context optimization, Collaborate with data teams, Collaborate with product teams, Translate financial datasets, Mentor engineers, Raise technical bar", "teamCollaboration" : "Data teams; Product teams", "domainKnowledge" : "Financial intelligence; Financial datasets; AI-native engineering", "domainList" : [ "financial-intelligence", "financial-datasets", "ai-native-engineering" ], "domainSpecificKnowledge" : [ "Financial intelligence", "Financial datasets", "AI-native engineering" ], "toolProficiency" : [ "LangChain", "LangGraph", "GraphQL", "MCP", "Cursor", "Claude Code", "Devin", "Snowflake", "Dbt", "Kafka" ], "communicationSkills" : "Technical direction", "continuousLearning" : "Mentorship; Professional development", "problemSolvingSkills" : "Root cause analysis", "qualificationsBasic" : "8+ years software engineering, Build production-scale systems, Design and ship AI systems, Hands-on agentic AI workflows, Expertise with modern AI tooling, Fluency in AI-native development, Understanding of AI evaluation, Advanced SQL proficiency, Advanced Python proficiency", "qualificationsPreferred" : "Familiarity with distributed systems, Familiarity with event-driven systems, Familiarity with Kafka, Familiarity with CDC pipelines, Familiarity with APIs, Technical leadership, Mentoring engineers, Driving technical direction", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "## Accountabilities Design, build, and deploy production-grade agentic AI systems that power advisor-facing financial intelligence products. Own end-to-end delivery of AI features, including agent orchestration, memory systems, evaluation frameworks, and production hardening. Architect scalable AI workflows that ensure reliability, observability, and performance across distributed systems. Develop and implement evaluation frameworks to measure, improve, and optimize agent behavior at scale. Leverage agentic AI tools and frameworks to accelerate development velocity and improve engineering productivity. Drive best practices for AI-native engineering, including prompt design, multi-agent orchestration, and context optimization. Collaborate with data and product teams to translate complex financial datasets into meaningful AI-driven insights. Mentor engineers and contribute to raising the technical bar across AI system design and delivery. Requirements: 8+ years of software engineering experience, with deep expertise in building production-scale systems. Proven experience designing and shipping AI or machine learning systems into production environments. Strong hands-on experience with agentic AI workflows, including orchestration, memory systems, and evaluation design. Expertise with modern AI tooling and frameworks such as LangChain, LangGraph, GraphQL, and MCP. Fluency in AI-native development environments and tools (e.g., Cursor, Claude Code, Devin or similar). Strong understanding of evaluation methodologies for AI systems and performance measurement at scale. Advanced proficiency in data engineering and analysis using SQL and Python, with experience in platforms like Snowflake and dbt. Familiarity with distributed data and event-driven systems (e.g., Kafka, CDC pipelines, APIs) is highly desirable. Strong technical leadership, communication skills, and a track record of mentoring engineers and driving technical direction. Benefits: Competitive compensation range: $200,000 – $220,000 base salary plus annual bonus target 4% 401(k) employer match to support long-term financial planning Comprehensive medical, dental, and vision insurance for employees and families Health Savings Account (HSA) or Flexible Spending Account (FSA) options Generous paid time off including 3 weeks vacation, sick leave, and 11 company holidays Remote-friendly culture with opportunities for in-person collaboration and team events Free financial planning services and employee financial wellness support Parental leave and pet insurance options to support family well-being Strong focus on learning, mentorship, and continuous professional development. ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Staff AI Execution Engineer. Skills: AI Execution, Agentic AI, Production systems. Design production-grade AI systems. Build production-grade AI systems", "postedDate" : "2026-06-15T06:48:16.015", "createdAt" : "2026-06-15T06:48:16.015", "lastUpdated" : "2026-06-16T12:33:21.952", "ingestTimestamp" : "2026-06-16T03:22:31.904", "mongoId" : "6a30511af292fd229cefa70e", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 200000, "salaryAnnualMax" : 220000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Prompt design", "Multi-agent orchestration", "Context optimization", "Data engineering", "Data analysis", "Performance measurement", "Leadership", "Communication skills", "AI Execution", "Agentic AI", "Production systems", "System design", "AI system design", "Delivery management", "Financial intelligence", "Financial datasets", "AI-native engineering", "LangChain", "LangGraph", "GraphQL", "MCP", "Cursor", "Claude Code", "Devin", "Snowflake", "Dbt", "Kafka" ], "skillCount" : 27, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Lead", "dataQualityScore" : 0.8888889, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "FinTech", "llmIndustryConfidence" : 0.98 }, { "id" : "69f8687c4c40e2acd1f7f46b", "title" : "AI & Digital Research Librarian", "company" : "SMU", "salary" : { "min" : 54581.0, "max" : 85496.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "TX-Dallas", "locations" : [ "TX-Dallas" ], "certifications" : [ "GCP Professional Data Engineer", "AWS Data Analytics", "Databricks Certified", "Dbt Certified" ], "timestamp" : "2026-06-16T01:56:46.970", "fingerprint" : "9e89c314d9b2579231e260ceaa6144ea413cf18e477ef18f8c4dd3bd53878f09", "source" : "taleo", "language" : "en", "applyUrl" : "https://smu.taleo.net/careersection/ex/jobdetail.ftl?job=76272", "externalId" : "76272", "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", "technicalSkills" : "SQL, Python, R, Tableau, Power BI, Snowflake, BigQuery, Redshift, Databricks, Dbt, Fivetran, Airflow, Delta Lake, Scikit-learn, TensorFlow, PyTorch, XGBoost, LightGBM, Hugging Face, MLflow, AWS, GCP, Azure", "professionalSkills" : [ "Quantitative analysis", "Data engineering", "Machine learning", "Business intelligence", "Analytics engineering" ], "hardSkillsList" : [ "Statistical methods", "Modelling skills" ], "hardSkills" : [ { "name" : "Statistical methods", "level" : "intermediate" }, { "name" : "Modelling skills", "level" : "intermediate" } ], "majorSkills" : "Data science, Data engineering, ML/AI, Business intelligence", "majorSkillsList" : [ "Data science", "Data engineering", "ML/AI", "Business intelligence" ], "coreResponsibilities" : "Develop and implement data models, Build and maintain data pipelines, Perform statistical analysis, Develop machine learning models, Create business intelligence dashboards, Collaborate with stakeholders, Ensure data quality, Optimize data infrastructure", "teamCollaboration" : "Cross-functional teams; Stakeholders", "toolProficiency" : [ "Dbt Cloud" ], "qualificationsBasic" : "5+ years of experience, Bachelor's degree, Proficiency in SQL, Proficiency in Python or R", "qualificationsPreferred" : "Master's degree or PhD, Experience with cloud platforms, Experience with ML frameworks, Experience with data warehousing", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Salary Range: $54,581.40 – $60,646.00 Commensurate with the Rank of Librarian 1 $66,193.20 – $73,548.00 Commensurate with the Rank of Librarian 2 $76,946.40 – $85,496.00 Commensurate with the Rank of Librarian 3 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: This role is an on-campus, in-person position. SMU Libraries seeks a collaborative and forward-thinking AI & Digital Research Librarian to lead and expand support for artificial intelligence-enabled research and digital scholarship initiatives. The ideal candidate is comfortable working in partnership with faculty, students, and campus colleagues and thrives in the iterative nature of the research process, where exploration, experimentation, and refinement are essential to discovery. This position is situated within the Research & Digital Strategy unit of SMU Libraries, which brings together the Norwick Center for Digital Solutions (nCDS) and the Research & Scholarly Initiatives (RSI) team to support AI-enabled and digitally driven research. The unit collaborates with faculty, students, and staff on artificial intelligence and machine learning, research data management, open access publishing, scholarly repositories, and digital scholarship, while connecting researchers with SMU Libraries’ distinctive special collections through digitization and digital preservation to advance innovative, technology-informed research. Building on the success of SMU Libraries’ 2025-2026 AI for Research cohorts of faculty and graduate students, this position will support new and ongoing projects that incorporate AI to advance innovative solutions in research and teaching. Working in partnership with faculty, students, librarians, and Office of Information Technology (OIT) staff, the librarian will support prompt engineering, prototype research workflows, and advise on AI-enabled research environments. This role will further solidify the Libraries’ position as a trusted research partner while ensuring alignment with SMU’s new strategic framework that will launch in fall 2026. This is an exciting time to join SMU Libraries as it continues to invest in innovative spaces and partnerships that support scholarship. The AI & Digital Research Librarian will be housed in the Research Lab within the Rees-Jones Library of the American West, a dynamic hub where researchers will engage with SMU Libraries’ special collections and develop projects that integrate rare and archival materials with emerging technologies, including AI and machine learning. In this role, the AI & Digital Research Librarian will design and lead programming, workshops, and research support services within the lab, fostering interdisciplinary collaboration and enabling researchers to explore new methods of discovery, analysis, and creative expression. SMU is a nationally ranked private research university in Dallas, TX, with eight degree-granting schools. SMU Libraries includes six libraries on the main campus and one library at our satellite location in Taos, NM. SMU Libraries and the SMU campus is dedicated to diversity and inclusion. We seek to hire a person who shares our values of a diverse and equitable workplace based on teamwork with a proactive and positive approach in all that we do. Essential Functions: AI Research Strategy and Service Design Assist researchers with prompt engineering to enable AI-assisted workflows. Evaluate commercial and open-source AI tools for research applicability, usability, and risk. Test retrieval-augmented and generative approaches. Translate researcher needs into clearly defined use cases and service models. Digital Scholarship Initiatives Collaborate on digital research projects by contributing expertise on AI, data management, and project management. Advise researchers on tools for data-driven scholarship and emerging scholarly formats. Support text analysis, data visualization, and digital mapping research methods. Support research projects that engage SMU Libraries’ digital collections. AI Infrastructure and Research Systems Collaborate with OIT and library systems teams to define requirements and use cases for AI-enabled research environments. Work with digital collections staff to identify, evaluate, and potentially develop AI tools for metadata and description workflows. Serve as liaison between researchers and technical teams to ensure infrastructure decisions align with research needs. Instruction and AI Literacy In collaboration with subject librarians, design and deliver workshops and instruction materials for AI literacy in research. Educate users on limitations and biases of AI systems. Support the integration of AI awareness and AI literacy within research and information literacy programming. Collaborate with library colleagues to develop internal guidance on the evaluation, adoption, and use of AI tools. Professional Development Continue professional growth through publishing, presentations, or participation and leadership in professional organizations. Serves on or chairs library, university and professional organization committees as appropriate. Engage with and contribute to national conversations relating to AI and digital research, demonstrating a thorough understanding of trends. Education and Experience: Required Qualifications: Master’s degree in Library and Information Science or advanced degree in other relevant or related field. Demonstrated experience in engaging with evolving AI/ML tools in teaching and/or research. Demonstrated experience collaborating on digital scholarship or digital research initiatives. Demonstrated experience providing instruction, consultations, or workshops in an academic setting. Demonstrated ability to evaluate and explain complex technical concepts to diverse audiences. Strong verbal and written communication. Preferred Qualifications: PhD, Ed.D., D.L.S., or other terminal doctoral degree in a relevant field Preferred. Project management experience. Strong knowledge of AI platforms and concepts such as vibe coding and bot construction as they apply to academic research, teaching, and/or libraries. Experience working collaboratively across library and IT environments. Knowledge of programming languages such as Python and R and frameworks such as Hugging Face and TensorFlow. Experience working with Special Collections, archives, or primary source materials in digital contexts. Knowledge of copyright, intellectual property, and other ethical considerations in digital and AI-enabled scholarship. Experience with digital scholarship tools that support text analysis, data visualization, and/or GIS/digital mapping. Candidates hired at the rank of Librarian 2 will require at least 2 years of work experience in an academic setting or research library. Candidates hired at the rank of Librarian 3 will require at least 5 years of experience in an academic setting or a research library. Knowledge, Skills and Abilities: Candidate must demonstrate strong interpersonal and verbal communication skills, with the ability to communicate broadly across the University and develop and maintain effective relationships with a wide range of constituencies. Must also demonstrate strong written communication skills. Candidate must possess strong problem-solving skills with the ability to identify and analyze problems, as well as devise solutions. Must also have strong organizational, planning and time management skills. Physical and Environmental Demands: Sit for long periods of time Deadline to Apply: Open until filled. Applications submitted by May 27, 2026 will receive priority consideration. To be considered for this position, applicants are required to submit: A resume or CV, A cover letter that addresses the education and experience required and preferred for this position. EEO Statement SMU is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, age, disability, genetic information, veteran status, sexual orientation, or gender identity and expression. 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" : "AI & Digital Research Librarian at SMU. Skills: Data science, Data engineering, ML/AI, Business intelligence. Develop and implement data models. Build and maintain data pipelines", "createdAt" : "2026-06-14T20:43:03.626", "lastUpdated" : "2026-06-16T01:56:46.970", "ingestTimestamp" : "2026-06-14T20:43:03.626", "mongoId" : "69f8687c4c40e2acd1f7f46b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 54581, "salaryAnnualMax" : 85496, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Statistical methods", "Modelling skills", "Data science", "Data engineering", "ML/AI", "Business intelligence", "Quantitative analysis", "Machine learning", "Analytics engineering", "GCP Professional Data Engineer", "AWS Data Analytics", "Databricks Certified", "Dbt Certified", "Dbt Cloud" ], "skillCount" : 14, "jobCategory" : "engineering", "jobSubcategory" : "data", "seniorityLevel" : "Mid", "dataQualityScore" : 0.6666667, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Education", "llmIndustryConfidence" : 0.95 }, { "id" : "6a3079f6f292fd229c0367c3", "title" : "Senior/Staff AI Research Engineer", "company" : "Hume AI", "industry" : "Technology", "salary" : { "min" : 180000.0, "max" : 350000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "New York, New York, United States", "locations" : [ "New York", "New York", "United States", "Remote", "San Jose", "California", "United States" ], "timestamp" : "2026-06-16T10:12:55.552", "fingerprint" : "0316c807b4e2300d094e4b29fd4e1cd02a1e32ee4ea30abe2cf9494ac020be04", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/humeai/jobs/4003488008", "externalId" : "4003488008", "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" : 2, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Python, PyTorch", "professionalSkills" : [ "System design", "Model training", "Data collection", "Data preprocessing", "Data analysis", "Inference", "Benchmarking" ], "hardSkillsList" : [ "Speech-language models", "Transformer models", "Large-scale datasets" ], "hardSkills" : [ { "name" : "Speech-language models", "level" : "intermediate" }, { "name" : "Transformer models", "level" : "intermediate" }, { "name" : "Large-scale datasets", "level" : "intermediate" } ], "majorSkills" : "AI research, Speech-language models, Model training", "majorSkillsList" : [ "AI research", "Speech-language models", "Model training" ], "coreResponsibilities" : "Build software systems, Support distributed model training, Support inference, Support benchmarking, Support data collection, Support data storage, Support data preprocessing, Support data analysis, Solve AI research problems", "teamCollaboration" : "AI research team", "domainKnowledge" : "Speech-language models; Human values in AI; Empathic AI", "domainList" : [ "speech-language-models", "human-values-in-ai", "empathic-ai" ], "domainSpecificKnowledge" : [ "Speech-language models", "Human values in AI", "Empathic AI" ], "innovationCreativity" : "R&D projects", "problemSolvingSkills" : "AI research problems", "qualificationsBasic" : "Python ecosystem expertise, Production-ready code experience, 2+ years transformer model training", "qualificationsPreferred" : "PhD preferred, Specific ML framework experience, Cloud platform certs", "remoteFriendly" : true, "rawDescription" : "Hume AI is seeking talented researchers and engineers interested in working with our AI research team to build state-of-the-art speech-language models (SLMs). Our new SLM training method—reinforcement learning from human expression (RLHE)—learns human preferences from behavior in millions of audio and video recordings, making SLMs superhumanly helpful, interesting, funny, eloquent, honest, and altruistic. Join us in the heart of New York City and contribute to our endeavor to ensure that AI is guided by human values, the most pivotal challenge (and opportunity) of the 21st century. About Us Hume AI is a Series B startup dedicated to building artificial intelligence that is directly optimized for human well-being. As the first company to release speech language models, we’re focused on expanding our research to encompass audio understanding models and evaluation platforms for enterprises. Our goal is to enable a future in which technology draws on an understanding of human emotional expression to better serve human goals. As part of our mission, we also conduct groundbreaking scientific research, publish in leading scientific journals like Nature, and support a non-profit, The Hume Initiative, that has released the first concrete ethical guidelines for empathic AI (www.thehumeinitiative.org). You can learn more about us on our website (https://hume.ai/) and read about us in WIRED, Forbes, and Venturebeat. About the Role We are looking for talented researchers and engineers interested in working with our team to build state-of-the-art audio models and evaluation tools. In this role, you will build out software systems that support distributed model training, inference, and benchmarking as well as massive-scale data collection, storage, preprocessing, and analysis. You will be working to solve some of today’s most exciting AI research problems at industry scale. Requirements Expertise in the Python ecosystem and popular ML libraries and tools (e. g. PyTorch) Experience writing robust and maintainable production-ready code Comfort iterating quickly on new and uncertain research directions 2+ years of experience training and/or fine-tuning transformer models with large-scale datasets of text, audio, image, and/or video data Application Note Please apply only to the position that best aligns with your qualifications. If you submit multiple applications or have applied within the past 6 months, only your initial submission will be considered. Annual Salary $180,000—$350,000 USD", "summaryDescription" : "Senior/Staff AI Research Engineer at Hume AI. Skills: AI research, Speech-language models, Model training. Build software systems. Support distributed model training", "postedDate" : "2026-06-16T01:19:33.752", "createdAt" : "2026-06-16T01:19:33.752", "lastUpdated" : "2026-06-16T10:12:55.552", "ingestTimestamp" : "2026-06-16T01:19:33.752", "mongoId" : "6a3079f6f292fd229c0367c3", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 180000, "salaryAnnualMax" : 350000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Speech-language models", "Transformer models", "Large-scale datasets", "AI research", "Model training", "System design", "Data collection", "Data preprocessing", "Data analysis", "Inference", "Benchmarking", "Human values in AI", "Empathic AI" ], "skillCount" : 13, "jobCategory" : "engineering", "jobSubcategory" : "data", "seniorityLevel" : "Senior", "dataQualityScore" : 1.0, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.98 }, { "id" : "6a307727f292fd229c022d75", "title" : "Staff Platform Engineer, AI Enablement", "company" : "Zocdoc", "industry" : "Healthcare", "salary" : { "min" : 250000.0, "max" : 400000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Staff Platform Engineer, AI Enablement in the US, adjusted for executive seniority and the technology industry." }, "location" : "USA Remote", "locations" : [ "USA Remote" ], "timestamp" : "2026-06-16T12:13:28.509", "fingerprint" : "bab76a6574bd2f4e868487e11509ff498b0d19dcd1837d29f9313308f0358bf0", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/zocdoc/jobs/7994223", "externalId" : "7994223", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Python, Java, Go, Kubernetes, Docker, AWS, GCP, Terraform, SQL, NoSQL, CI/CD, Git", "professionalSkills" : [ "System design", "Architecture design", "API design" ], "hardSkillsList" : [ "Distributed systems", "Scalability", "Reliability", "Performance tuning" ], "hardSkills" : [ { "name" : "Distributed systems", "level" : "intermediate" }, { "name" : "Scalability", "level" : "intermediate" }, { "name" : "Reliability", "level" : "intermediate" }, { "name" : "Performance tuning", "level" : "intermediate" } ], "majorSkills" : "Platform engineering, AI enablement, Cloud infrastructure", "majorSkillsList" : [ "Platform engineering", "AI enablement", "Cloud infrastructure" ], "coreResponsibilities" : "Design and build scalable infrastructure, Develop and maintain CI/CD pipelines, Implement monitoring and alerting solutions, Automate operational tasks, Collaborate with AI/ML teams, Improve system reliability and performance, Troubleshoot production issues, Contribute to platform architecture decisions", "teamCollaboration" : "Cross-functional teams; AI/ML engineers; Software engineers", "projectManagementSkills" : [ "Agile methodologies" ], "domainKnowledge" : "AI/ML platforms; Cloud-native architecture; Distributed systems", "domainList" : [ "ai-ml-platforms", "cloud-native-architecture", "distributed-systems" ], "domainSpecificKnowledge" : [ "AI/ML platforms", "Cloud-native architecture", "Distributed systems" ], "toolProficiency" : [ "Kubernetes", "Docker", "AWS", "GCP", "Terraform", "Prometheus", "Grafana", "GitLab CI", "Jenkins" ], "documentationSkills" : "Technical documentation", "problemSolvingSkills" : "Root cause analysis; Troubleshooting", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Our Mission Healthcare should work for patients, but it doesn’ t. In their time of need, they call down outdated insurance directories. Then wait on hold. Then wait weeks for the privilege of a visit. Then wait in a room solely designed for waiting. Then wait for a surprise bill. In any other consumer industry, the companies delivering such a poor customer experience would not survive. But in healthcare, patients lack market power. Which means they are expected to accept the unacceptable. Zocdoc’s mission is to give power to the patient. To do that, we’ve built the leading healthcare marketplace that makes it easy to find and book in-person or virtual care in all 50 states, across +200 specialties and +12k insurance plans. By giving patients the ability to see and choose, we give them power. In doing so, we can make healthcare work like every other consumer sector, where businesses compete for customers, not the other way around. In time, this will drive quality up and prices down. We’re 18 years old and the leader in our space, but we are still just getting started. If you like solving important, complex problems alongside deeply thoughtful, driven, and collaborative teammates, read on. Your Impact on Our Mission At Zocdoc, we're on a mission to give power to the patient -- and that starts with enabling our engineering teams to build and ship software safely, efficiently, and with confidence. As a Staff Platform Engineer, you will design, build, and improve the foundational systems, tooling, and paved roads that create leverage across our engineering organization; accelerating delivery while improving reliability, consistency, and developer experience. This role sits within the Infrastructure organization. You will collaborate across the business to turn platform strategy into practical, adoptable solutions. The role emphasizes hands-on technical leadership with meaningful input into platform direction, with the goal of reducing friction across the development lifecycle and enabling teams to focus on improving healthcare access rather than infrastructure scaffolding. You will play a key role in how developers at Zocdoc build, test, and deploy software. You'll do this through agentic AI, self-service capabilities, composable platform patterns, and opinionated but flexible paved roads. Your work will abstract operational complexity, improve testability and safety, and streamline the developer journey across frontend, backend, and mobile surfaces. You'll Enjoy This Role If You... Enjoy building platforms that enable productivity, consistency, and autonomy Are motivated by making other engineers more effective, not just shipping your own features Like designing cohesive developer experiences that teams actually want to adopt Care deeply about developer empathy, usability, and reducing cognitive load Prefer solving real problems through thoughtful design, iteration, and collaboration Are comfortable influencing peers and adjacent teams through clear communication and working code Find satisfaction in building systems that scale predictably and help other engineers succeed Enjoy learning and teaching others about leveraging AI-based technologies to achieve real-world results Your Day to Day Design and build platform services and solutions that are secure, scalable, and intentionally easy to use -- including CI/CD pipelines, developer tooling, and shared infrastructure patterns Contribute to the technical direction of Zocdoc's internal developer platform, including paved roads, tooling, and shared workflows Collaborate across teams to understand real developer pain points, validate platform bets, and drive adoption of platform capabilities Own and deliver high-impact platform investments end to end -- from problem framing through implementation and rollout Improve measurable developer outcomes such as build times, deployment safety, feedback loops, and operational simplicity Champion platform-as-product thinking by treating internal engineers as users and continuously refining the developer experience based on their feedback Advance platform capabilities in AI-assisted development, helping shape how engineers use AI in their daily workflows with the right guardrails for safety, quality, and testability Mentor engineers and technologies across the business and raise the bar for technical design and code quality Ensure platform patterns align with security, compliance, and reliability expectations without becoming a bottleneck You'll Be Successful in This Role If You... Have 7+ years of experience building or evolving internal developer platforms, productivity tooling, or CI/CD systems used by multiple teams Have designed and operated distributed systems in AWS or similar cloud environments Bring strong judgment around platform abstractions and APIs; knowing when to standardize and when to stay flexible Can take ambiguous problems, break them into deliverable pieces, and drive them to measurable outcomes Communicate technical trade-offs clearly and build consensus with peers and stakeholders Treat adoption as a first-class engineering problem, not an afterthought Are motivated by enabling other engineers to build reliable, scalable, and secure systems with confidence Value learning, curiosity, and operational excellence, and model those qualities for the team Strategy vs. Execution Split ~20% Strategy and Influence (contributing to platform direction, participating in cross-team alignment, surfacing trade-offs and priorities) ~80% Hands-On Technical Leadership (designing and building platform capabilities, reviewing architecture and code, partnering with teams on adoption and iteration) Benefits: Flexible work environment for those based in NYC (Role is open to remote) Unlimited Vacation 100% paid employee health benefit options (including medical, dental, and vision) 401(k) with employer funded match Corporate wellness program with Wellhub Sabbatical leave (for employees with 5+ years of service) Competitive paid parental leave and fertility/family planning reimbursement Cell phone reimbursement Employee Resource Groups and ZocClubs to promote shared community and belonging Great Place to Work Certified Zocdoc is committed to fair and equitable compensation practices. Salary ranges are determined through alignment with market data. Base salary offered is determined by a number of factors including the candidate’s experience, qualifications, and skills. Certain positions are also eligible for variable pay and/or equity; your recruiter will discuss the full compensation package details. NYC Base Salary Range $210,000—$270,000 USD About us Zocdoc is the country’s leading digital health marketplace that helps patients easily find and book the care they need. Each month, millions of patients use our free service to find nearby, in-network providers, compare choices based on verified patient reviews, and instantly book in-person or video visits online. Providers participate in Zocdoc’s Marketplace to reach new patients to grow their practice, fill their last-minute openings, and deliver a better healthcare experience. Founded in 2007 with a mission to give power to the patient, our work each day in pursuit of that mission is guided by our six core values. Zocdoc is a private company backed by some of the world’s leading investors, and we believe we’re still only scratching the surface of what we plan to accomplish. Zocdoc is a mission-driven organization dedicated to building teams as diverse as the patients and providers we aim to serve. In the spirit of one of our core values - Together, Not Alone, we are a company that prides itself on being highly collaborative, and we believe that diverse perspectives, experiences and contributors make our community and our platform better. We’re an equal opportunity employer committed to providing employees with a work environment free of discrimination and harassment. Applicants are considered for employment regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity, gender expression, sexual orientation, age, citizenship, marital or parental status, disability, veteran status, or any other class protected by applicable laws. Job Applicant Privacy Notice", "summaryDescription" : "Staff Platform Engineer, AI Enablement at Zocdoc. Skills: Platform engineering, AI enablement, Cloud infrastructure. Design and build scalable infrastructure. Develop and maintain CI/CD pipelines", "postedDate" : "2026-06-16T01:17:16.656", "createdAt" : "2026-06-16T01:17:16.656", "lastUpdated" : "2026-06-16T12:13:28.509", "ingestTimestamp" : "2026-06-16T01:17:16.656", "mongoId" : "6a307727f292fd229c022d75", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 250000, "salaryAnnualMax" : 400000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Distributed systems", "Scalability", "Reliability", "Performance tuning", "Platform engineering", "AI enablement", "Cloud infrastructure", "System design", "Architecture design", "API design", "Agile methodologies", "AI/ML platforms", "Cloud-native architecture", "Kubernetes", "Docker", "AWS", "GCP", "Terraform", "Prometheus", "Grafana", "GitLab CI", "Jenkins" ], "skillCount" : 22, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Executive", "dataQualityScore" : 1.0, "daysOld" : 0, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2b975774d8ee00a0816d87", "title" : "Regulatory Affairs Specialist", "company" : "Medtronic", "industry" : "Healthcare Technology", "salary" : { "min" : 74400.0, "max" : 111600.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "Lafayette, Colorado, United States of America", "locations" : [ "Lafayette, Colorado, United States of America" ], "timestamp" : "2026-06-14T22:31:35.949", "fingerprint" : "51e99d8de79e647776ac98b5952486577e1eb3993a91a092b65faec11e75290b", "source" : "workday", "language" : "en", "applyUrl" : "https://medtronic.wd1.myworkdayjobs.com/RedeploymentMedtronicCareers/job/Lafayette-Colorado-United-States-of-America/Regulatory-Affairs-Specialist---On-site_R68155", "externalId" : "R68155", "industryFunction" : { }, "locationPoint" : "36.18589,-85.71609", "structuredLocations" : [ { "city" : "Lafayette", "state" : "Colorado", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "39.9935959,-105.0897050" } ], "locationText" : "Lafayette, Colorado, United States", "employmentType" : "FULL_TIME", "professionalSkills" : [ "Regulatory affairs", "Market access", "Compliance oversight", "Risk management", "Legal analysis" ], "hardSkillsList" : [ "Regulatory submissions", "Electronic submissions", "Document management", "Data analysis" ], "softSkillsList" : [ "Mentoring" ], "hardSkills" : [ { "name" : "Regulatory submissions", "level" : "intermediate" }, { "name" : "Electronic submissions", "level" : "intermediate" }, { "name" : "Document management", "level" : "intermediate" }, { "name" : "Data analysis", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Mentoring" } ], "majorSkills" : "Regulatory affairs, Regulatory submissions, Compliance", "majorSkillsList" : [ "Regulatory affairs", "Regulatory submissions", "Compliance" ], "coreResponsibilities" : "Prepare regulatory submissions, Publish regulatory submissions, Perform quality control on submissions, Deliver regulatory submissions, Produce submissions using electronic publishing tools, Manage enterprise-wide regulatory management systems, Coordinate regulatory systems, Support regulatory system users, Maintain regulatory system data, Develop training for colleagues, Deliver training for colleagues, Contribute to regulatory systems development, Contribute to regulatory systems implementation, Contribute to regulatory systems improvement, Provide input to system design, Provide input to system enhancements, Prepare paper submissions, Prepare electronic submissions, Submit supplements, Submit amendments, Submit annual reports, Submit general correspondence, Submit adverse event reports, Submit promotional material filings, Track submissions, Index submissions, Archive paper submissions, Archive electronic submissions, Collaborate cross-functionally, Collect required information, Resolve issues, Provide regulatory status updates, Report regulatory status to leadership", "teamCollaboration" : "Cross-functional teams; Diverse stakeholder groups", "projectManagementSkills" : [ "Project delivery" ], "domainKnowledge" : "Regulatory requirements; Electronic document systems; Regulatory management systems; Marketing authorization applications; Electronic common technical documents; Document management standards; Quality requirements; Spinal implants; Navigation systems; Robotic guidance systems; Advanced imaging; Data-driven planning tools; Surgical procedures; Neurological conditions; Spinal conditions", "domainList" : [ "regulatory-requirements", "electronic-document-systems", "regulatory-management-systems", "marketing-authorization-applications", "electronic-common-technical-documents", "document-management-standards", "quality-requirements", "spinal-implants", "navigation-systems", "robotic-guidance-systems", "advanced-imaging", "data-driven-planning-tools", "surgical-procedures", "neurological-conditions", "spinal-conditions" ], "domainSpecificKnowledge" : [ "Regulatory requirements", "Electronic document systems", "Regulatory management systems", "Marketing authorization applications", "Electronic common technical documents", "Document management standards", "Quality requirements", "Spinal implants", "Navigation systems", "Robotic guidance systems", "Advanced imaging", "Data-driven planning tools", "Surgical procedures", "Neurological conditions", "Spinal conditions" ], "toolProficiency" : [ "Electronic publishing tools", "Electronic document systems" ], "communicationSkills" : "Report-outs to leadership", "documentationSkills" : "Regulatory documentation", "problemSolvingSkills" : "Troubleshooting", "specialRequirements" : "Minimum 4 days a week onsite", "outcomesObjectives" : "Support timely market access; Support ongoing compliance; Ensure work alignment with policies; Ensure work alignment with procedures; Ensure work alignment with quality standards; Enhance surgical precision; Streamline workflows; Support improved patient outcomes", "qualificationsBasic" : "Baccalaureate degree, 2 years of relevant experience", "qualificationsPreferred" : "Experience with regulatory data systems, Experience preparing regulatory submissions, Attention to detail, Organizational skills, Ability to manage multiple projects, Ability to meet deadlines, Effective written communication skills, Effective verbal communication skills", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "We anticipate the application window for this opening will close on - 20 Jun 2026 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. # **A Day in the Life** Across our global Neuroscience organization, we advance care for some of medicine’s most complex neurological and spinal conditions. By combining innovative technology, data-driven insights, and deep clinical expertise, we partner with physicians and health systems to improve how patients are treated and supported throughout their care journey. Our Cranial & Spinal Technologies (CST) Operating Unit develops and delivers an integrated ecosystem of spinal implants, navigation and robotic guidance systems, advanced imaging, and data-driven planning tools for complex spine and cranial procedures. Platforms such as AiBLE™ connect these technologies to enhance surgical precision, streamline workflows, and support improved patient outcomes worldwide. Check us out on LinkedIn: [Medtronic CST](https://www.linkedin.com/company/medtronic-brain-and-spine-therapies/posts/?feedView=all) The Regulatory Affairs Specialist is an individual contributor role within the Cranial & Spinal Technologies Operating Unit, responsible for planning and delivering regulatory projects that support timely market access and ongoing compliance. This position works cross‑functionally to prepare, publish, and manage high‑quality regulatory submissions and related documentation, leveraging specialized knowledge of regulatory requirements and electronic document systems. The role may mentor colleagues or provide direction to lower‑level professionals while ensuring work is delivered in alignment with Medtronic policies, procedures, and quality standards. At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary. Responsibilities may include the following and other duties may be assigned. Key Responsibilities * Prepare, publish, perform quality control, and deliver paper and electronic components of regulatory submissions, including initial large marketing authorization applications and electronic common technical documents (eCTD). * Produce submissions using electronic publishing tools in compliance with document management standards and applicable regulatory/quality requirements. * Manage activities related to enterprise-wide regulatory management systems, including systems coordination, user support, and data maintenance. * Develop and deliver training for colleagues on regulatory systems, tools, and related processes. * Contribute to the development, implementation, and continuous improvement of regulatory systems and processes, including input to system design and enhancements. * Prepare, submit, track, index, and archive paper and electronic submissions such as supplements, amendments, annual reports, general correspondence, adverse event reports, and promotional material filings. * Collaborate cross‑functionally (e.g., with R&D, Quality, Clinical, Marketing) to collect required information, resolve issues, and provide clear regulatory status updates, including report‑outs to leadership. Minimum Qualifications * Baccalaureate degree * Minimum of 2 years of relevant experience in a regulated industry Preferred Qualifications * Experience with regulatory or other complex data systems, including data entry, reporting, and troubleshooting. * Demonstrated ability to analyze data and metrics to inform decision‑making and process improvements. * Strong cross‑functional collaboration skills and experience working with diverse stakeholder groups. * Experience preparing or contributing to regulatory submissions (e.g., eCTD, marketing applications, annual reports, amendments, or adverse event reporting). * Strong attention to detail, organizational skills, and ability to manage multiple projects and deadlines. * Effective written and verbal communication skills, including clear report‑outs to leadership. For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required. **Physical Job Requirements** The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. **U.S. Work Authorization & Sponsorship ** At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment. Join us in our mission to alleviate pain, restore health, and extend life—where your unique background and perspective are valued. # **Benefits & Compensation** **Medtronic offers a competitive Salary and flexible Benefits Package** A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Salary ranges for U.S (excl. PR) locations (USD):$74,400.00 - $111,600.00 This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). ## ## The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others). The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums). Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico. Further details are available at the link below: [Medtronic benefits and compensation plans](https://www3.benefitsolver.com/benefits/BenefitSolverView?page_name=signon&co_num=30601&co_affid=medtronic) # **About Medtronic** # We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. Learn more about our business, mission, and our commitment to diversity [here](http://www.medtronic.com). It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities. If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find [here](https://www.medtronic.com/content/dam/medtronic-wide/public/united-states/employee-support-services/careers/la-county-legal-notice.pdf) a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.", "summaryDescription" : "Regulatory Affairs Specialist at Medtronic. Skills: Regulatory affairs, Regulatory submissions, Compliance. Prepare regulatory submissions. Publish regulatory submissions", "postedDate" : "2026-06-11T08:15:05.156", "createdAt" : "2026-06-12T08:15:05.054", "lastUpdated" : "2026-06-14T22:31:35.949", "ingestTimestamp" : "2026-06-12T08:15:05.054", "mongoId" : "6a2b975774d8ee00a0816d87", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://medtronic.wd1.myworkdayjobs.com/RedeploymentMedtronicCareers/job/Lafayette-Colorado-United-States-of-America/Regulatory-Affairs-Specialist---On-site_R68155", "salaryAnnualMin" : 74400, "salaryAnnualMax" : 111600, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Regulatory submissions", "Electronic submissions", "Document management", "Data analysis", "Mentoring", "Regulatory affairs", "Compliance", "Market access", "Compliance oversight", "Risk management", "Legal analysis", "Project delivery", "Regulatory requirements", "Electronic document systems", "Regulatory management systems", "Marketing authorization applications", "Electronic common technical documents", "Document management standards", "Quality requirements", "Spinal implants", "Navigation systems", "Robotic guidance systems", "Advanced imaging", "Data-driven planning tools", "Surgical procedures", "Neurological conditions", "Spinal conditions", "Electronic publishing tools" ], "skillCount" : 28, "jobCategory" : "engineering", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare Technology" }, { "id" : "6a2b975774d8ee00a0816dc2", "title" : "Regulatory Affairs Specialist", "company" : "Medtronic", "industry" : "Healthcare", "salary" : { "min" : 48400.0, "max" : 72600.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : false }, "location" : "Galway, County Galway, Ireland", "locations" : [ "Galway, County Galway, Ireland" ], "timestamp" : "2026-06-14T23:54:36.471", "fingerprint" : "fac813e9e6d9ffe167e859bbec88b01444f4069a2a1b94ff6fe0385364b7ae5c", "source" : "workday", "language" : "en", "applyUrl" : "https://medtronic.wd1.myworkdayjobs.com/RedeploymentMedtronicCareers/job/Galway-County-Galway-Ireland/Regulatory-Affairs-Specialist_R68241", "externalId" : "R68241", "industryFunction" : { }, "locationPoint" : "53.27245,-9.05095", "structuredLocations" : [ { "city" : "Galway", "state" : "County Galway", "country" : "Ireland", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "53.2744122,-9.0490601" } ], "locationText" : "Galway, County Galway, Ireland", "employmentType" : "FULL_TIME", "professionalSkills" : [ "Regulatory affairs", "Risk management", "Legal analysis", "Compliance oversight" ], "hardSkillsList" : [ "Regulatory requirements", "Device change assessment", "Regulatory submissions", "License renewal", "Annual registrations", "Product changes", "Process changes", "Supportive documentation", "International submissions" ], "softSkillsList" : [ "Negotiation", "Interpersonal skills", "Organizational skills", "Time management skills" ], "hardSkills" : [ { "name" : "Regulatory requirements", "level" : "intermediate" }, { "name" : "Device change assessment", "level" : "intermediate" }, { "name" : "Regulatory submissions", "level" : "intermediate" }, { "name" : "License renewal", "level" : "intermediate" }, { "name" : "Annual registrations", "level" : "intermediate" }, { "name" : "Product changes", "level" : "intermediate" }, { "name" : "Process changes", "level" : "intermediate" }, { "name" : "Supportive documentation", "level" : "intermediate" }, { "name" : "International submissions", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Negotiation" }, { "name" : "Interpersonal skills" }, { "name" : "Organizational skills" }, { "name" : "Time management skills" } ], "majorSkills" : "Regulatory affairs, Medical devices, Global regulatory requirements", "majorSkillsList" : [ "Regulatory affairs", "Medical devices", "Global regulatory requirements" ], "coreResponsibilities" : "Lead submissions, Compile submission materials, Compile license renewal materials, Compile annual registration materials, Address agency questions, Provide support to marketed products, Review labeling, Review product changes, Review process changes, Review supportive documentation, Prepare submissions for FDA, Prepare reports for FDA, Provide support for international submissions, Maintain worldwide regulatory requirements proficiency, Establish RA department relationships, Maintain RA department relationships, Establish cross functional team relationships, Maintain cross functional team relationships, Develop positive relationships with device reviewers, Maintain positive relationships with device reviewers, Assist in negotiations with FDA, Assist in negotiations with regulatory agencies", "teamCollaboration" : "Cross functional teams; RA department; Device reviewers", "domainKnowledge" : "Class II devices; Class III devices; Medical Device Directive; Medical Device Regulation", "domainList" : [ "class-ii-devices", "class-iii-devices", "medical-device-directive", "medical-device-regulation" ], "domainSpecificKnowledge" : [ "Class II devices", "Class III devices", "Medical Device Directive", "Medical Device Regulation" ], "communicationSkills" : "Written communication; Verbal communication", "documentationSkills" : "Regulatory filings", "qualificationsBasic" : "NFQ Level 8 Bachelor’s degree, 2 years relevant experience, Master’s degree no experience", "qualificationsPreferred" : "Experience with Class II/III devices, Experience with FDA requirements, Experience with MDD, Experience with MDR, Experience with medicinal consultations, Experience with global regulatory requirements, Experience with quality standards", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. # **A Day in the Life** **Medtronic** At Medtronic, we value what makes you unique. Be part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations. **Our Purpose** Peripheral Vascular Health therapies are a critical part of the Medtronic vascular portfolio, treating patients with a broad range of conditions, including Peripheral and Carotid Disease, End Stage Renal Disease, Peripheral Embolization, and Superficial and Deep Venous Disease. This position will reside in the Peripheral Vascular Health organization that cares for millions of patients globally with life-enhancing therapies. The Regulatory Affairs Specialist is responsible for worldwide regulatory activities for new and existing Class II and Class III devices and provide advice on regulatory requirements. The Regulatory Affairs Specialist is responsible for assessing device changes for regulatory implications and for performing relevant regulatory actions in support of the implementation of these changes. This role focuses on a wide variety of regulatory tasks to allow the Regulatory Affairs Specialist to make the most of his/her existing knowledge base while growing his RA skill set daily working within a collaborative team environment. **_Come for a job, stay for a career!_** **A Day in The Life Of:** Responsibilities may include the following and other duties may be assigned. * Lead or compile all materials required in submissions, license renewal and annual registrations. Work with engineers and technical experts to address questions from regulatory agencies. * Provide support to currently marketed products as necessary. This includes reviewing labeling, product or process changes as well as supportive documentation for changes requiring RA agency review. Prepare submissions and reports for FDA or provide support and documentation for international submissions. * Maintain proficiency in worldwide regulatory requirements. * Establish and maintain good relationships within the RA department, cross functional teams and assist in developing and maintaining positive relationships with device reviewers through verbal and written communications. * May assist in negotiations with the FDA or other regulatory agencies for defined projects. * Other tasks, as assigned. **Key Skills & Experience** * Minimum NFQ Level 8 Bachelor’s degree in Regulatory Science, Pharmaceutical, Biomedical or related medical/scientific field with minimum 2 years of relevant experience in medical device industry. * Or Master’s degree in Regulatory Science, Pharmaceutical, Biomedical or related medical/scientific field with no prior experience. Nice to have: * Experience working with Class II/III medical devices. * Experience with FDA requirements, guidance documents, Medical Device Directive (MDD), Medical Device Regulation (MDR), medicinal consultations and/or other global regulatory requirements and quality standards. * Effective negotiation and written/oral communication skills. * Effective interpersonal, organizational and time management skills. * Effective team member. * Detail-oriented **Medtronic offer a competitive salary and flexible Benefits Package** #INDJ #LI-Onsite **Physical Job Requirements** The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. # **Benefits & Compensation** **Medtronic offers a competitive Salary and flexible Benefits Package** A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik: Ireland: 48,400.00 EUR - 72,600.00 EUR | This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). # **About Medtronic** # We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. Learn more about our business, mission, and our commitment to diversity [here](http://www.medtronic.com)", "summaryDescription" : "Regulatory Affairs Specialist at Medtronic. Skills: Regulatory affairs, Medical devices, Global regulatory requirements. Lead submissions. Compile submission materials", "postedDate" : "2026-06-11T08:11:52.704", "createdAt" : "2026-06-12T08:11:52.519", "lastUpdated" : "2026-06-14T23:54:36.471", "ingestTimestamp" : "2026-06-12T08:11:52.519", "mongoId" : "6a2b975774d8ee00a0816dc2", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://medtronic.wd1.myworkdayjobs.com/RedeploymentMedtronicCareers/job/Galway-County-Galway-Ireland/Regulatory-Affairs-Specialist_R68241", "salaryBand" : "30k-50k", "hasSalary" : false, "allSkills" : [ "Regulatory requirements", "Device change assessment", "Regulatory submissions", "License renewal", "Annual registrations", "Product changes", "Process changes", "Supportive documentation", "International submissions", "Negotiation", "Interpersonal skills", "Organizational skills", "Time management skills", "Regulatory affairs", "Medical devices", "Global regulatory requirements", "Risk management", "Legal analysis", "Compliance oversight", "Class II devices", "Class III devices", "Medical Device Directive", "Medical Device Regulation" ], "skillCount" : 23, "jobCategory" : "other", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "id" : "6a2cc3ad74d8ee00a0a0a1e7", "title" : "Corporate Counsel, AI & Digital Health", "company" : "Amazon.com Services LLC", "industry" : "Legal, legal", "salary" : { "min" : 208200.0, "max" : 900000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Seattle, Washington, USA", "locations" : [ "Seattle, Washington, USA" ], "timestamp" : "2026-06-15T09:10:10.779", "fingerprint" : "27f9047e91904274adfe7c908a33e025e9b09b060242c2d7180e6c7e94ab1c1d", "source" : "amazon", "language" : "en", "applyUrl" : "https://account.amazon.jobs/jobs/10447967/apply", "externalId" : "59a3e530-8e08-49b6-aef2-132032afef43", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Seattle", "state" : "Washington", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "47.6038321,-122.3300620" } ], "locationText" : "Seattle, Washington, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Legal guidance", "Risk management", "Compliance oversight", "Legal analysis" ], "hardSkillsList" : [ "Data use", "AI legislation", "Industry standards" ], "hardSkills" : [ { "name" : "Data use", "level" : "intermediate" }, { "name" : "AI legislation", "level" : "intermediate" }, { "name" : "Industry standards", "level" : "intermediate" } ], "majorSkills" : "AI legal, Digital health, Healthcare AI", "majorSkillsList" : [ "AI legal", "Digital health", "Healthcare AI" ], "coreResponsibilities" : "Provide legal support, Counsel on data use, Counsel on treatment, Counsel on compliance, Develop governance frameworks, Implement governance frameworks, Partner with product teams, Partner with engineering teams, Partner with clinical teams, Monitor AI legislation, Advise on AI legislation, Advise on industry standards", "teamCollaboration" : "Product teams; Engineering teams; Clinical teams", "domainKnowledge" : "Artificial intelligence; Emerging technology; Healthcare; AI/ML technologies; NIST rules; ONC rules", "domainList" : [ "artificial-intelligence", "emerging-technology", "healthcare", "ai-ml-technologies", "nist-rules", "onc-rules" ], "domainSpecificKnowledge" : [ "Artificial intelligence", "Emerging technology", "Healthcare", "AI/ML technologies", "NIST rules", "ONC rules" ], "qualificationsBasic" : "5+ years legal experience, Juris Doctor, Membership in one state bar", "qualificationsPreferred" : "Corporate law firm experience, In-house legal experience, AI/ML legal experience, Healthcare regulatory experience, Digital health legal experience", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Amazon Health Services Legal is seeking an experienced attorney to serve as legal counsel supporting Health AI products and services. This role will provide strategic legal guidance on the development, deployment, and scaling of AI/ML technologies within Amazon's health businesses, including One Medical and Amazon Pharmacy. You will need to combine deep artificial intelligence and emerging technology with a passion for reinventing healthcare. You will operate at the intersection of innovation and compliance, enabling teams to move fast while maintaining compliance in one of the most highly regulated industries. Key job responsibilities - Provide day-to-day legal support for Health AI and other AI-related clinical and product efforts. - Counsel on data use, treatment, and compliance obligations - Develop and implement responsible AI governance frameworks - Partner with product, engineering, and clinical teams throughout the product lifecycle - Monitor and advise on evolving AI legislation (state and federal) and industry standards (e.g., NIST, ONC rules), helping to develop AI policy for healthcare in the US Basic Qualifications: - 5+ years of post bar admission legal experience - Juris Doctor and membership in one state bar or equivalent Preferred Qualifications: - Experience of a mix of corporate law firm and in-house work - Experience in Artificial Intelligence/Machine Learning (AI/ML) Standards Law - Experience advising on healthcare regulatory matters - Experience counseling product and engineering teams - Experience navigating regulatory frameworks - Experience drafting and negotiating agreements Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status. 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. The base salary range for this position is listed below. Your Amazon package will include sign-on payments and restricted stock units (RSUs). Final compensation will be determined based on factors including experience, qualifications, and location. Amazon also offers comprehensive benefits including health insurance (medical, dental, vision, prescription, Basic Life & AD&D insurance and option for Supplemental life plans, EAP, Mental Health Support, Medical Advice Line, Flexible Spending Accounts, Adoption and Surrogacy Reimbursement coverage), 401(k) matching, paid time off, and parental leave. Learn more about our benefits at https://amazon.jobs/en/benefits . USA, WA, SEATTLE - 153,900.00 - 208,200.00 USD annually", "summaryDescription" : "Corporate Counsel, AI & Digital Health at Amazon.com Services LLC. Skills: AI legal, Digital health, Healthcare AI. Provide legal support. Counsel on data use", "postedDate" : "2026-06-12T00:00:00.000", "createdAt" : "2026-06-14T05:24:48.761", "lastUpdated" : "2026-06-15T09:10:10.779", "ingestTimestamp" : "2026-06-14T05:24:48.761", "mongoId" : "6a2cc3ad74d8ee00a0a0a1e7", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.jobs/jobs/10447967/apply", "salaryAnnualMin" : 208200, "salaryAnnualMax" : 900000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Data use", "AI legislation", "Industry standards", "AI legal", "Digital health", "Healthcare AI", "Legal guidance", "Risk management", "Compliance oversight", "Legal analysis", "Artificial intelligence", "Emerging technology", "Healthcare", "AI/ML technologies", "NIST rules", "ONC rules" ], "skillCount" : 16, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Senior", "dataQualityScore" : 1.0, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2af78274d8ee00a073d614", "title" : "Regulatory Affairs Manager", "company" : "AstraZeneca", "industry" : "Healthcare", "salary" : { "min" : 1000000.0, "max" : 1800000.0, "currency" : "EGP", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Manager in the Pharma industry in Egypt, adjusted for seniority and company size." }, "location" : "Egypt", "locations" : [ "Egypt" ], "timestamp" : "2026-06-14T22:43:26.705", "fingerprint" : "30bf7bd4001e469bf25bccf02bbe126ff8ef263b558f8ae5481c7401de5aed97", "source" : "workday", "language" : "en", "applyUrl" : "https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/Egypt/Regulatory-Affairs-Manager_R-254239-1", "externalId" : "R-254239", "industryFunction" : { }, "locationPoint" : "26.8206,30.8025", "structuredLocations" : [ { "country" : "Egypt", "continent" : "af", "workMode" : "onsite" } ], "locationText" : "Egypt", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceLevel" : "Manager", "professionalSkills" : [ "Regulatory strategy", "Lifecycle management", "Product registration", "Labeling", "Post-approval changes", "Regulatory dossiers", "Health authority interactions", "Agency communications", "Compliance", "Quality culture", "Change control", "Market continuity", "Product compliance", "Risk assessments", "Transparent decision-making", "Business planning" ], "hardSkillsList" : [ "Regulatory filing", "Dossier preparation", "Response writing", "Submission management", "Labeling development", "Change assessment" ], "hardSkills" : [ { "name" : "Regulatory filing", "level" : "intermediate" }, { "name" : "Dossier preparation", "level" : "intermediate" }, { "name" : "Response writing", "level" : "intermediate" }, { "name" : "Submission management", "level" : "intermediate" }, { "name" : "Labeling development", "level" : "intermediate" }, { "name" : "Change assessment", "level" : "intermediate" } ], "majorSkills" : "Regulatory strategy, Submission management, Health authority engagement, Compliance", "majorSkillsList" : [ "Regulatory strategy", "Submission management", "Health authority engagement", "Compliance" ], "coreResponsibilities" : "Develop regulatory strategies, Implement regulatory strategies, Lead dossier preparation, Coordinate dossier preparation, Review regulatory dossiers, Submit regulatory dossiers, Manage variations, Manage renewals, Respond to questions, Ensure activities align with regulations, Ensure activities align with company policies, Maintain inspection readiness, Partner with internal teams, Gather required documentation, Align regulatory plans, Resolve issues quickly, Contribute to labeling development, Review product labeling, Maintain product labeling, Assess regulatory impact, Define required submissions, Deliver required submissions, Build submission timelines, Maintain submission timelines, Build regulatory risk assessments, Maintain regulatory risk assessments, Enable transparent decision-making, Inform business planning", "teamCollaboration" : "Cross-functional collaboration; Partner with internal teams", "projectManagementSkills" : [ "Project management", "Manage multiple deadlines", "Coordinate contributors", "Escalate risks" ], "domainKnowledge" : "Global regulations; Product registration; Labeling regulations; Post-approval changes; Lifecycle management; Regulatory frameworks; Health authority guidelines; Manufacturing regulations; Quality regulations; Safety regulations", "domainList" : [ "global-regulations", "product-registration", "labeling-regulations", "post-approval-changes", "lifecycle-management", "regulatory-frameworks", "health-authority-guidelines", "manufacturing-regulations", "quality-regulations", "safety-regulations" ], "domainSpecificKnowledge" : [ "Global regulations", "Product registration", "Labeling regulations", "Post-approval changes", "Lifecycle management", "Regulatory frameworks", "Health authority guidelines", "Manufacturing regulations", "Quality regulations", "Safety regulations" ], "communicationSkills" : "Written communication; Verbal communication; Clear documentation; Influence stakeholders; Agency communications; Rapid responses", "documentationSkills" : "Regulatory documentation; Dossier preparation; Labeling text; Submission timelines; Risk assessments", "continuousLearning" : "Keep learning; Deepen expertise; Explore new areas; Coaching; Mentorship", "problemSolvingSkills" : "Resolve issues; Problem solving", "outcomesObjectives" : "Faster approvals; Secure timely registrations; Optimize product value; Deliver right-first-time quality; Maintain market continuity; Accelerate patient access", "qualificationsBasic" : "Bachelor’s degree in pharmacy, Experience in regulatory affairs, Understanding of regulatory frameworks, Written and verbal communication skills, Project management skills, Focus on details, accuracy, documentation quality, and compliance", "qualificationsPreferred" : "Strategic thinking, Regulatory judgment, Stakeholder management, Planning and prioritization, Risk assessment, Problem solving, Cross functional collaboration, Decision making", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Job title: Regulatory Affairs Manager** **Introduction to role:** Are you ready to turn complex global regulations into faster approvals that put life-changing medicines in patients’ hands? In this role, you will lead regulatory strategy and execution across development and lifecycle, guiding submissions and health authority interactions to secure timely registrations. You will translate evolving requirements into decisive plans that align teams, reduce risk, and enable confident, on-time delivery. Can you see yourself shaping the path from first dossier outline to final approval while building capability around you? **Accountabilities:** * **Regulatory Strategy:** Develop and implement regulatory strategies for product registration, labeling, post-approval changes, and lifecycle management to accelerate approvals and optimize product value. * **Submission Management:** Lead or coordinate the preparation, review, and submission of regulatory dossiers, variations, renewals, and responses to questions, delivering right-first-time quality and region-specific compliance. * **Health Authority Engagement:** Plan, support, or lead agency communications, including meeting requests, briefing documents, and rapid, clear responses and follow-up that build credibility and trust. * **Compliance and Standards:** Ensure all activities align with regulations, guidance, company policies, and submission standards; champion inspection readiness and a culture of quality. * **Cross-Functional Collaboration:** Partner with internal teams to gather required documentation, align regulatory plans with project milestones, and resolve issues quickly to protect timelines. * **Labeling Support:** Contribute to the development, review, and maintenance of product labeling, artwork, and regulatory text to ensure accuracy and alignment with scientific and commercial objectives. * **Change Control and Lifecycle Management:** Assess regulatory impact of manufacturing, quality, safety, or labeling changes; define and deliver required submissions to maintain market continuity and product compliance. * **Planning and tracking:** Build and maintain submission timelines, regulatory risk assessments, and documentation that enable transparent decision-making and inform business planning. **Essential Skills/Experience:** * Bachelor’s degree in pharmacy. * Strong experience in regulatory affairs * Strong understanding of relevant regulatory frameworks and other applicable requirements. * Strong written and verbal communication skills, including the ability to prepare clear regulatory documentation and influence stakeholders. * Strong Project management skills with the ability to manage multiple deadlines, coordinate contributors, and escalate risks appropriately. * Strong focus on details, accuracy, documentation quality, and compliance. **Desirable Skills/Experience:** * Strategic thinking * Regulatory judgment * Stakeholder management * Planning and prioritization * Risk assessment * Problem solving * Cross functional collaboration * Decision making **Why AstraZeneca?** Here you will work with specialists who are empowered to influence decisions across the enterprise, combining bold ideas with disciplined delivery to move fast without compromising on quality. We bring unexpected teams together—policy shapers, scientists, technologists, and regulatory experts—to challenge assumptions and spark better solutions. You will be encouraged to keep learning, deepen your expertise, and explore new areas with coaching and mentorship that match your ambition. We value kindness alongside ambition, and we balance a dynamic, change-driven environment with the rigour required by government procedures—so your work directly accelerates patient access while advancing your career. If you are ready to lead regulatory strategy that turns science into approvals and measurable patient impact, take the next step and shape what comes next with us today! **Date Posted** 10-يونيو-2026 **Closing Date** 29-يونيو-2026 AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.", "summaryDescription" : "Regulatory Affairs Manager at AstraZeneca. Skills: Regulatory strategy, Submission management, Health authority engagement, Compliance. Develop regulatory strategies. Implement regulatory strategies", "postedDate" : "2026-06-11T02:23:58.366", "createdAt" : "2026-06-12T02:23:58.319", "lastUpdated" : "2026-06-14T22:43:26.705", "ingestTimestamp" : "2026-06-12T02:23:58.319", "mongoId" : "6a2af78274d8ee00a073d614", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/Egypt/Regulatory-Affairs-Manager_R-254239-1", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Regulatory filing", "Dossier preparation", "Response writing", "Submission management", "Labeling development", "Change assessment", "Regulatory strategy", "Health authority engagement", "Compliance", "Lifecycle management", "Product registration", "Labeling", "Post-approval changes", "Regulatory dossiers", "Health authority interactions", "Agency communications", "Quality culture", "Change control", "Market continuity", "Product compliance", "Risk assessments", "Transparent decision-making", "Business planning", "Project management", "Manage multiple deadlines", "Coordinate contributors", "Escalate risks", "Global regulations", "Labeling regulations", "Regulatory frameworks", "Health authority guidelines", "Manufacturing regulations", "Quality regulations", "Safety regulations" ], "skillCount" : 34, "jobCategory" : "other", "seniorityLevel" : "manager", "dataQualityScore" : 1.0, "daysOld" : 3, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare" }, { "id" : "6a3055d9f292fd229cf223c5", "title" : "Staff Product Manager (AI Agents)", "company" : "Traba", "industry" : "EPD", "salary" : { "min" : 210000.0, "max" : 250000.0, "currency" : "USD", "frequency" : "Yearly" }, "location" : "New York City, NY", "locations" : [ "New York City, NY", "San Francisco" ], "timestamp" : "2026-06-16T12:08:32.880", "fingerprint" : "f1b1124f8d499e113e657ed7969bbbe049196ca0c400349a2cfd823b27f4549e", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/traba/c2cb9715-573b-4519-b210-6176165db638/application", "externalId" : "c2cb9715-573b-4519-b210-6176165db638", "industryFunction" : { }, "structuredLocations" : [ { "city" : "New York City", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.7127281,-74.0060152" }, { "city" : "San Francisco", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "37.7879363,-122.4075201" } ], "locationText" : "New York City, New York, United States; San Francisco, California, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "coreResponsibilities" : "Define product strategy, Develop product roadmap, Write user stories, Collaborate with cross-functional teams", "teamCollaboration" : "Cross-functional teams", "projectManagementSkills" : [ "Roadmap planning" ], "rawDescription" : "ABOUT TRABA Traba is building the AI operating layer for the industrial supply chain. We started in the workforce space because contingent labor is the biggest operational pain point our manufacturing and logistics customers face. We used it to embed ourselves inside their daily operations and create a far better customer experience through technology. Now those same customers are pulling us beyond staffing into the broader operational workflows that run their facilities. That foundation gave us proprietary data from millions of shifts and deep enterprise relationships. But our edge is more than data. By connecting to the systems running across every facility and activating the workers already on our platform to execute against them, we are building applied AI that drives real productivity gains and transforms how the global supply chain operates at scale. We are backed by Founders Fund, Khosla Ventures, and General Catalyst. THE ROLE We are looking for an entrepreneurial and experienced Product Manager to join as a founding member of the Agents team and help us build the next layer of Traba's product, an agentic platform that synthesizes the data flowing through our marketplace and operates autonomously inside our customers' supply chain workflows. Think Claude, but for Light Industrial businesses. You'll embed deeply in our customers' operations, design and ship production agents that understand context, reason through ambiguity, make decisions, and execute work on behalf of users. This is a true 0-to-1 product role operating at the frontier of applied AI. You will work directly with founders, product engineers, ML teams, and early design partners to define workflows, shape product strategy, and build products while the underlying model ecosystem continues changing beneath us. The assumptions, capabilities, and constraints will evolve rapidly and the product will evolve with them. This role reports directly to our VP of Product. WHAT YOU’LL DO - Architect and steward product strategy for Traba’s AI agent platform - Solve complex customer problems by balancing user needs, technical constraints, and evolving AI capabilities - Write detailed product requirements and partner deeply with product engineers and ML teams - Rapidly validate and prototype ideas alongside customers and design partners - Design agent systems that reason through workflows, orchestrate tools, maintain context, and execute meaningful work - Define product behavior, evaluation systems, and quality frameworks that improve reliability and performance - Use data to uncover patterns and answer key product and system questions - Evolve our AI product portfolio with a deep understanding of model capabilities and system architecture - Visualize and communicate complex concepts from system behavior and evaluations to user experiences and business impact - Socialize your work across all levels and departments while synthesizing diverse stakeholder feedback WHAT WE’RE LOOKING FOR Real agent builder. You have launched customer-facing AI products where the system took meaningful actions on behalf of users. We are intentionally setting a high bar here. Shipping AI features, copilots, chat interfaces, wrappers, or lightweight LLM integrations alone is not enough. You understand agents that execute workflows, orchestrate systems, use tools, maintain context, and perform work autonomously. 0-to-1 operator. You have built products from scratch with real customers and understand the realities of finding product market fit. You have launched, rebuilt, changed direction, killed ideas, and iterated toward signals. You are comfortable creating structures where no playbook exists. AI-native problem solver. You move quickly in environments where models evolve constantly and assumptions regularly break. You understand that building AI products often means navigating prompt rewrites, model shifts, reliability tradeoffs, and capability cliffs. First-principles thinker. You spend equal time thinking about why, how, and what. You understand that strong product judgment often comes from deeply understanding systems and constraints rather than applying generic playbooks. Customer-embedded builder. You believe the best products are built shoulder-to-shoulder with customers. You have experience deeply embedding with early customers, understanding workflows firsthand, and rapidly shipping based on direct feedback loops. Experience with forward deployed environments or customer-embedded product development models is highly valued. Technical depth. You are comfortable operating alongside ML engineers and highly technical teams as peers. You can understand evaluations, reason through system tradeoffs, prototype ideas, and participate deeply in technical conversations. You do not need to be an ex-engineer, but you should have strong technical instincts and enjoy getting into the details. Builder mentality. Inventive and scrappy problem solver. You move quickly, embrace ambiguity, and know how to create meaningful outcomes without relying on giant teams or excessive process. Deeply collaborative. You work seamlessly across engineering, ML, operations, design, leadership, and customers to bring new products to life. WHAT YOU’LL BRING - 7 – 10 years of experience as a Product Manager - Evidence of launching products from scratch and driving meaningful customer outcomes - Experience building AI-native products or customer-facing agent systems - Strong technical abilities with the ability to work deeply with engineering and ML teams - Ability to read evaluations, reason through system performance, and prototype ideas - Experience operating in highly ambiguous startup environments with fast iteration cycles - Deep familiarity with AI tools and hands-on experience building with modern AI systems - Desire to work at a startup and cover an exceptionally wide surface area - A strong work ethic and desire to build a category-defining company BENEFITS - \uD83D\uDCC8 Start-up equity - \uD83D\uDCB0 Competitive Salary - \uD83E\uDE7A 100% Paid health, dental & vision coverage - \uD83C\uDF7D️ Dinner Provided via Grubhub & stocked kitchen for NY employees - \uD83D\uDE8D Commuter benefit - \uD83C\uDFA4 Team building events - \uD83C\uDFCB\uD83C\uDFFD Gympass Benefit - \uD83C\uDF34 Flexible PTO - ✚✚ Additional: One Medical Membership, Gympass, HSA via Optum, Talkspace, Health Advocate, Teledoc Health SALARY RANGE DETAILS The compensation range for this position is set between $180,000 and $210,000, reflecting our market analysis and other relevant considerations. However, exceptions may be made for candidates with qualifications that significantly differ from those outlined in the job description.We also offer a highly competitive equity package designed to ensure you share meaningfully in the long-term success and upside of the business. The position is based onsite in New York City or San Francisco, five days per week, giving you the opportunity to collaborate closely with a high-performing team in a fast-paced, energetic environment. Being in person supports real-time decision-making, stronger teamwork, and the kind of creative problem-solving that drives meaningful impact. EQUAL OPPORTUNITY EMPLOYER Traba is dedicated to promoting Equal Opportunity employment practices. We evaluate all applicants without discrimination based on race, color, religion, creed, national origin, age, sex, gender, marital status, sexual orientation and identity, genetic information, veteran status, citizenship, or any other characteristics that are legally protected by local, state, or federal regulations. We encourage applicants from a variety of backgrounds, experiences, and skill sets. OUR VALUES Dream Big - We are on a path to change the world for the better. We create and communicate a bold direction that inspires a life-changing vision. We don’t sacrifice long-term value for short-term results. Olympian’s Work Ethic - Changing the world never comes easy. We work harder, longer, and smarter, not just two out of three. We put everything we have on the field. Growth Mindset - We confront the toughest challenges head-on and persevere. Sometimes we fail, but we brush ourselves off, adapt, learn, and push forward with resilience. Customer Obsession - We go the extra mile for our workers and businesses. We remain focused on delivering high-quality products and services that solve this massive and overlooked industries’ problems WHAT IS LIGHT INDUSTRIAL LABOR? Light industrial flexible staffing is a $50B labor market that encompasses entry-level jobs in warehouses & distribution centers. These workers pack boxes, load trucks, and manage warehouse operations to keep supply chains running at peak efficiency. Privacy Notice for CA Applicants https://traba.work/privacy-notice-ca-applicants", "summaryDescription" : "Staff Product Manager (AI Agents) at Traba. Define product strategy. Develop product roadmap", "createdAt" : "2026-06-16T00:26:38.658", "lastUpdated" : "2026-06-16T12:08:32.880", "ingestTimestamp" : "2026-06-16T00:26:38.658", "mongoId" : "6a3055d9f292fd229cf223c5", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 210000, "salaryAnnualMax" : 250000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Roadmap planning" ], "skillCount" : 1, "jobCategory" : "product", "jobSubcategory" : "product_management", "seniorityLevel" : "Senior", "dataQualityScore" : 0.8888889, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2a7bcf74d8ee00a06646d5", "title" : "Regulatory Affairs Pharmacovigilance Manager", "company" : "myTomorrows", "industry" : "Operations", "salary" : { "min" : 150000.0, "max" : 210000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Manager in Regulatory Affairs Pharmacovigilance in the US Biotech industry, adjusted for remote work and manager seniority." }, "location" : "US, Remote ", "locations" : [ "US, Remote ", "Canada ", "United Kingdom " ], "timestamp" : "2026-06-12T21:09:59.500", "fingerprint" : "fa17ff3265ab175b2775203bc20d283ce45e4fc14eb759a025c91522d4c5455b", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/myTomorrows/f90bd4cd-00ad-40da-bd95-80bca7efe655/application", "externalId" : "f90bd4cd-00ad-40da-bd95-80bca7efe655", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Manager", "professionalSkills" : [ "Regulatory strategy", "Regulatory affairs", "Pharmacovigilance", "Expanded Access Programs" ], "hardSkillsList" : [ "Regulatory submissions", "Dossier preparation", "Regulatory documentation" ], "softSkillsList" : [ "Problem solver" ], "hardSkills" : [ { "name" : "Regulatory submissions", "level" : "intermediate" }, { "name" : "Dossier preparation", "level" : "intermediate" }, { "name" : "Regulatory documentation", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Problem solver" } ], "majorSkills" : "Regulatory Affairs, Pharmacovigilance, Expanded Access", "majorSkillsList" : [ "Regulatory Affairs", "Pharmacovigilance", "Expanded Access" ], "coreResponsibilities" : "Support regulatory strategies for EAPs, Act as RA/PV expert, Communicate with clients, Submit to Health Authorities, Attend cross-functional meetings, Attend audits, Prepare regulatory dossiers for EAPs, Compile regulatory dossiers for EAPs, Submit regulatory dossiers for EAPs, Provide input for regulatory strategy, Support setting up EAPs, Support executing EAPs, Collaborate with Commercial team, Ensure compliant handling of regulatory activities, Ensure compliant handling of pharmacovigilance activities, Stay up to date on global laws, Stay up to date on regulations, Stay up to date on guidelines, Assist in drafting documentation, Assist in reviewing documentation, Assist in maintaining documentation, Liaise with Pharmacovigilance provider, Contribute to maintaining SOPs, Contribute to maintaining QIs, Contribute to maintaining CAPAs", "teamCollaboration" : "Working with Medical Affairs; Working with Program Management; Working with Quality Assurance; Working with Supply Chain; Collaborating across teams; Working in cross-functional environment", "domainKnowledge" : "Expanded Access Regulations; Biologicals; Cell therapies; Synthetic drugs; National legislation; International legislation", "domainList" : [ "expanded-access-regulations", "biologicals", "cell-therapies", "synthetic-drugs", "national-legislation", "international-legislation" ], "domainSpecificKnowledge" : [ "Expanded Access Regulations", "Biologicals", "Cell therapies", "Synthetic drugs", "National legislation", "International legislation" ], "toolProficiency" : [ "Microsoft 365", "Word", "Excel", "Teams", "SharePoint" ], "communicationSkills" : "Convey complex topics", "documentationSkills" : "Drafting documentation; Reviewing documentation; Maintaining documentation", "continuousLearning" : "Internal knowledge sharing", "problemSolvingSkills" : "Identify challenges; Suggest solutions", "qualificationsBasic" : "5 years relevant experience, Expanded Access experience, Working knowledge of Pharmacovigilance, Bachelor's or Master's degree, Experience with clients/external stakeholders, Reside within EST or CST time zones", "qualificationsPreferred" : "Knowledge of additional languages", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "About myTomorrows myTomorrows is a global health tech company dedicated to breaking down barriers for patients seeking treatment options.    We strive to enable earlier and better treatment access by bridging the gap between those searching for possible options, and the companies who develop them. We work closely with patients, healthcare professionals, trial sites, patient advocacy groups, and BioPharma – connecting key stakeholders in the drug development ecosystem.    We’ve developed a cutting-edge AI-powered technology platform that simplifies and streamlines access to drugs in development. To support our users and clients, we have a range of industry-expert specialized teams ready to help. Our services include clinical trial patient recruitment, Expanded Access Program management and Real-World Data collection.    With a global footprint spanning 134 countries, to date we’ve supported over 17,000 patients, 3,000 physicians and 350 sites, earning the trust of 60+ BioPharma companies. In October 2025, we closed a €25M investment with Avego Healthcare Capital to fuel our global ambitions and scale the business.   Join us in shaping the future of treatment access - making tomorrow’s therapies accessible for people who need them today. The opportunity: Regulatory Affairs & Pharmacovigilance Manager As the Regulatory Affairs and Pharmacovigilance Manager, you will be responsible for ensuring compliance of our processes with country-specific expanded access regulations globally. In this role, you'll be a key contributor to our regulatory and quality infrastructure, keeping us aligned with global legislation. You will be actively working together with Medical Affairs, Program Management, Quality Assurance, and Supply Chain and will report to the Director of Regulatory Affairs and Pharmacovigilance (Emily says hi). Geographic Requirement: For candidates in North America, to ensure seamless collaboration with our teams, applicants must reside within the EST or CST time zones. What you will do in this role: - Support the development and execution of regulatory strategies for Expanded Access Programs (EAPs) involving biologicals, cell therapies, and synthetic drugs. - Act as the Regulatory Affairs and Pharmacovigilance expert for communications with clients (pharmaceutical companies) and submissions to Health Authorities, as well as cross-functional meetings and audits. - Prepare, compile, and submit regulatory dossiers for cohort and named patient Expanded Access Programs (EAPs) on behalf of clients. - Provide input and support for the regulatory strategy for setting up and executing EAPs (e.g., where, when, and how). - Collaborate with the Commercial team to support new EAPs. - Ensure timely and compliant handling of all regulatory and pharmacovigilance activities related to EAPs. - Stay up to date on relevant global laws, regulations, and guidelines impacting EAPs. - Assist in drafting, reviewing, and maintaining regulatory documentation and templates. - Liaise with the Pharmacovigilance service provider to ensure alignment and compliance. - Contribute to maintaining department documentation such as SOPs (Standard Operating Procedures), QIs (Quality Incidents), and CAPAs (Corrective and Preventive Actions). What you bring to the table: - Approximately 5 years of relevant experience in Regulatory Affairs, including experience in Expanded Access. - Working knowledge of fundamental principles of Pharmacovigilance is required. - Solid understanding of national and international legislation and regulation relating to Expanded Access - A Bachelor’s or Master's degree in Life Sciences or a related field - Experience working directly with clients or external stakeholders in a professional setting - Strong communication skills (written and verbal) in English; able to convey complex topics clearly to both internal teams and external parties. Knowledge of additional languages is a plus - Comfortable collaborating across teams and working in a cross-functional environment - Proactive problem solver with the ability to identify potential regulatory or operational challenges early and suggest practical solutions - Familiarity with Microsoft 365 tools (e.g., Word, Excel, Teams, SharePoint) What we offer: - Impactful work that helps patients gain access to potentially lifesaving treatments. - International work environment, scale-up energy and flat organizational structure which encourages creativity and accountability. - Competitive salary, annual performance bonus and an Employee Stock Option Plan. - Great career development opportunities in a fast-growing company. - Learning and development budget alongside internal knowledge sharing sessions. - Hybrid working model if you're in the Netherlands. - Policies to support working parents. - Healthy lunch at the thriving Amsterdam office. - Unlimited access to professional guidance by certified psychologists via OpenUp - Enjoy monthly events hosted by our vibrant Culture Club as well as an annual ‘myTomorrowland’ company-wide celebration! Equal opportunities myTomorrows is an Equal Opportunity Employer and, beyond upholding discrimination-free practices, we are committed to cultivating a workplace where difference and diversity are protected and celebrated. The best work comes from our best selves, and we go to great lengths in supporting our team members to be just that. ", "summaryDescription" : "Regulatory Affairs Pharmacovigilance Manager at myTomorrows. Skills: Regulatory Affairs, Pharmacovigilance, Expanded Access. Support regulatory strategies for EAPs. Act as RA/PV expert", "postedDate" : "2026-06-11T16:28:23.449", "createdAt" : "2026-06-11T16:28:23.449", "lastUpdated" : "2026-06-12T21:09:59.500", "ingestTimestamp" : "2026-06-11T16:28:23.449", "mongoId" : "6a2a7bcf74d8ee00a06646d5", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 150000, "salaryAnnualMax" : 210000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Regulatory submissions", "Dossier preparation", "Regulatory documentation", "Problem solver", "Regulatory Affairs", "Pharmacovigilance", "Expanded Access", "Regulatory strategy", "Regulatory affairs", "Expanded Access Programs", "Expanded Access Regulations", "Biologicals", "Cell therapies", "Synthetic drugs", "National legislation", "International legislation", "Microsoft 365", "Word", "Excel", "Teams", "SharePoint" ], "skillCount" : 21, "jobCategory" : "operations", "jobSubcategory" : "regulatory-affairs-and-pharmacovigilance-management", "dataQualityScore" : 1.0, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare" }, { "id" : "6a2af78674d8ee00a073d6dd", "title" : "Senior Regulatory Affairs Associate", "company" : "AstraZeneca", "industry" : "Pharmaceutical", "salary" : { "min" : 135000.0, "max" : 195000.0, "currency" : "AUD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Regulatory Affairs Associate in Australia, adjusted for seniority and industry." }, "location" : "Australia", "locations" : [ "Australia" ], "timestamp" : "2026-06-14T18:57:04.686", "fingerprint" : "02487814fe2d5baba5e6d1da60de157458117c3a2a57238aac22b6b05963df93", "source" : "workday", "language" : "en", "applyUrl" : "https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/Australia--New-South-Wales/Senior-Regulatory-Affairs-Associate---Expression-of-Interest_R-253210", "externalId" : "R-253210", "industryFunction" : { }, "locationPoint" : "-25.2744,133.7751", "structuredLocations" : [ { "country" : "Australia", "continent" : "oc", "workMode" : "onsite" } ], "locationText" : "Australia", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Regulatory affairs", "Submission planning", "Lifecycle management", "Regulatory strategy", "Stakeholder management" ], "hardSkillsList" : [ "Regulatory submission", "PI/CMI drafting", "CMC assessment", "CDS assessment" ], "softSkillsList" : [ "Critical thinking" ], "hardSkills" : [ { "name" : "Regulatory submission", "level" : "intermediate" }, { "name" : "PI/CMI drafting", "level" : "intermediate" }, { "name" : "CMC assessment", "level" : "intermediate" }, { "name" : "CDS assessment", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Critical thinking" } ], "majorSkills" : "Regulatory affairs, TGA submissions, Product compliance", "majorSkillsList" : [ "Regulatory affairs", "TGA submissions", "Product compliance" ], "coreResponsibilities" : "Prepare and execute regulatory submission plans, Translate regulatory strategies into submissions, Provide operational regulatory input, Provide tactical regulatory input, Manage end-to-end submissions, Maintain product compliance, Lead regulatory project delivery, Meet business milestones, Meet patient access goals, Plan TGA submissions, Prepare TGA submissions, Manage TGA submissions, Ensure quality filing, Ensure on-time filing, Draft PI content, Draft CMI content, Negotiate PI content, Negotiate CMI content, Maintain PI content, Maintain CMI content, Optimise labels, Coordinate responses to TGA questions, Author responses to TGA questions, Manage agency interactions, Assess lifecycle changes, Implement lifecycle changes, Select regulatory pathways, Maintain compliance, Identify regulatory risks, Implement risk mitigations, Protect labels, Protect timelines, Protect supply continuity, Collaborate with global Regulatory Affairs, Collaborate with local stakeholders, Operate to GRP, Operate to GMDP, Operate to AZ GxP QMS, Complete training, Drive continuous compliance improvement, Work in line with AZ Code of Ethics, Work in line with OH&S policies, Maintain safe environment, Maintain inclusive environment, Maintain high-integrity environment", "teamCollaboration" : "Cross-functional teams; Global Regulatory Affairs; Local stakeholders", "projectManagementSkills" : [ "Project delivery" ], "domainKnowledge" : "Drug development process; Post-approval lifecycle management; TGA regulations; AZ GxP QMS", "domainList" : [ "drug-development-process", "post-approval-lifecycle-management", "tga-regulations", "az-gxp-qms" ], "domainSpecificKnowledge" : [ "Drug development process", "Post-approval lifecycle management", "TGA regulations", "AZ GxP QMS" ], "communicationSkills" : "Written communication; Verbal communication", "documentationSkills" : "PI content; CMI content", "continuousLearning" : "Lifelong learning; Growth and development", "problemSolvingSkills" : "Analytical thinking; Critical thinking", "outcomesObjectives" : "Achieve optimum label; Achieve earliest feasible patient availability", "qualificationsBasic" : "University degree in scientific discipline, Experience in Regulatory Affairs, Experience at health authority, Knowledge of drug development process, Knowledge of post-approval lifecycle management, Excellent written and verbal drafting/negotiating PI/CMI content, Analytical and critical thinking, Delivery and results orientation, Proven cross-functional collaboration, Stakeholder management, Customer focus, Ability to prioritise, Drive multiple submissions to deadlines", "qualificationsPreferred" : "Broader pharmaceutical experience, Demonstrated leadership of projects or teams, Influencing skills, Track record of shaping regulatory outcomes", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "We are actively building a talent pipeline for******Senior Regulatory Affairs Associate** positions If you’d like to be among the first to hear about these upcoming roles, we invite you to join our Talent Network. By registering, you’ll gain access to early notifications of vacancies, networking opportunities, and tailored insights to support your career development. Stay connected with us and secure your chance to be part of our future hiring initiatives. At AstraZeneca, we’re driven by the power of science and the promise of transformative medicines. Our Regulatory Affairs team turns scientific innovation into patient impact by securing timely, high‑quality approvals and optimised labels. Join us to shape regulatory outcomes that accelerate access for patients across Australia and beyond. **About the role** As a Senior Regulatory Affairs Associate, you will prepare and execute regulatory submission plans for allocated products and projects, translating agreed regulatory strategies into high‑quality, timely submissions to the TGA (and partnering with NZ where relevant). You’ll provide operational and tactical regulatory input to cross‑functional teams, manage end‑to‑end submissions, and maintain product compliance throughout the lifecycle. Success means balancing scientific rigor with commercial pragmatism to achieve an optimum label and the earliest feasible availability for patients. **What you’ll do** * Lead regulatory project delivery in Australia, providing operational and tactical Regulatory Affairs expertise to meet business milestones and patient access goals * Plan, prepare and manage simple and complex TGA submissions end to end, ensuring quality and on‑time filing * Draft, negotiate and maintain PI and CMI to reflect evolving clinical, safety and CMC data and optimise labels * Coordinate and author responses to TGA questions, managing agency interactions to progress approvals efficiently * Assess and implement lifecycle changes (CMC, CDS, PI), selecting appropriate regulatory pathways to maintain compliance * Identify regulatory risks and implement mitigations to protect labels, timelines and supply continuity * Collaborate with global Regulatory Affairs and local stakeholders (Quality, Supply Chain, Medical, Safety, Commercial) for aligned delivery * Operate to GRP, GMDP and AZ GxP QMS standards; complete training and drive continuous compliance improvement * Work in line with the AZ Code of Ethics and OH&S policies to maintain a safe, inclusive, high‑integrity environment **Essential skills and experience** * University degree in a scientific or related discipline. * Experience in Regulatory Affairs within the pharmaceutical industry or experience at a health authority. * Strong knowledge of the drug development process and post‑approval lifecycle management. * Excellent written and verbal communication; confident drafting/negotiating PI/CMI content. * Analytical and critical thinking with delivery and results orientation. * Proven cross‑functional collaboration and stakeholder management. * Customer focus with the ability to prioritise and drive multiple submissions to deadlines. **Desirable** * Broader pharmaceutical experience (e.g., Quality Control, Clinical Trial Management). * Demonstrated leadership of cross‑functional projects or teams. * Influencing skills with a track record of shaping regulatory outcomes. **Why AstraZeneca?** At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare. **Join Our Talent Network** Please join with a resume outlining your suitable experience or just your name and contact details if you don't have a resume handy and we'll follow up after the event to get your resume. **Where can I find out more?** * **Visit our Global Website** _-_[_https://www.astrazeneca.com/_](https://www.astrazeneca.com/) * **Follow AstraZeneca on LinkedIn**[ _https://www.linkedin.com/company/1603/_](https://www.linkedin.com/company/1603/) * **Follow us on Instagram** _–_[ _https://www.instragram.com/astrazeneca/_](https://www.instragram.com/astrazeneca/) _AstraZeneca in Australia has been formally recognised as an Employer of Choice for Gender Equality by the Workplace Gender Equality Agency (WGEA) and as a Gold Tier Employer within the Australian Workplace Equality Index (AWEI). Visit our ANZ Careers Page -_[_www.astrazeneca.com.au/careers.html_](https://www.astrazeneca.com.au/careers.html) _to learn more about our commitment to fostering a flexible, diverse, and inclusive environment._ _We recognise that any recruitment process may present challenges, if there is anything we can do to make our recruitment process more accessible for you, please le_ **Date Posted** 09-June-2026 **Closing Date** 12-June-2026 AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.", "summaryDescription" : "Senior Regulatory Affairs Associate at AstraZeneca. Skills: Regulatory affairs, TGA submissions, Product compliance. Prepare and execute regulatory submission plans. Translate regulatory strategies into submissions", "postedDate" : "2026-06-10T06:54:42.223", "createdAt" : "2026-06-12T06:54:42.170", "lastUpdated" : "2026-06-14T18:57:04.686", "ingestTimestamp" : "2026-06-12T06:54:42.170", "mongoId" : "6a2af78674d8ee00a073d6dd", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/Australia--New-South-Wales/Senior-Regulatory-Affairs-Associate---Expression-of-Interest_R-253210", "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "Regulatory submission", "PI/CMI drafting", "CMC assessment", "CDS assessment", "Critical thinking", "Regulatory affairs", "TGA submissions", "Product compliance", "Submission planning", "Lifecycle management", "Regulatory strategy", "Stakeholder management", "Project delivery", "Drug development process", "Post-approval lifecycle management", "TGA regulations", "AZ GxP QMS" ], "skillCount" : 17, "jobCategory" : "other", "seniorityLevel" : "senior", "dataQualityScore" : 1.0, "daysOld" : 4, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Pharmaceutical" }, { "id" : "6a30867df292fd229c080c3d", "title" : "Director of Digital Customer Experience & AI", "company" : "Banyan Software", "industry" : "SaaS", "salary" : { "min" : 200000.0, "max" : 300000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Director of Digital Customer Experience & AI in the US SaaS industry, adjusted for seniority and remote work." }, "location" : "United States", "locations" : [ "United States" ], "timestamp" : "2026-06-16T14:47:56.860", "fingerprint" : "0cc94726fdf48675e19addf255a03e4d1ce210f0e0f5383847d7a6deb7c254d7", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/banyansoftware/jobs/5163577007", "externalId" : "5163577007", "industryFunction" : { }, "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "remote" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "remoteFriendly" : true, "rawDescription" : "Banyan Software is the best permanent home for software businesses that serve specialized industries, their employees, and their customers. We are on a mission to acquire, build, and grow great companies worldwide, helping them modernize through shared AI expertise and operational discipline. The Banyan Software Foundation, endowed with $100 million in Banyan stock, leverages technology to build a greener and more equitable world. Banyan is Great Place to Work Certified, a five-time Inc. 5000 honoree, and a top 10 company on the Deloitte Technology Fast 500. Founded in 2016 and headquartered in Atlanta, Banyan operates more than 100 portfolio companies across North America, the UK, EU, and APAC. Director of Digital Customer Experience from answering questions to guiding workflows and executing tasks within our Microsoft Dynamics 365 Business Central– based platform. We are seeking a Director of Intelligent Customer Experience to lead the strategy, design, and continuous improvement of AI-powered customer interactions across the Loan Vision ecosystem. This role will own LV Luna not just as a platform, but as a customer-facing experience layer that shapes how clients learn, operate, and succeed with our solution. This is a techno-functional leadership role sitting within Customer Success, responsible for translating AI capabilities into practical, secure, and intuitive customer experiences. The ideal candidate blends customer empathy, process design, and technical fluency to deliver meaningful outcomes, not just technology. What You’ll Own • The end-to-end AI-driven customer experience, with LV Luna as a core interaction layer • Adoption, quality, and effectiveness of AI-assisted workflows across customers and internal teams • A scalable operating model for designing, testing, and improving AI-driven experiences (“AgentOps”) • The evolution of LV Luna from support assistance to workflow execution and operational enablement Key Responsibilities Customer Experience Strategy delivering real outcomes for customers and setting Loan Vision apart in the market. Diversity, Equity, Inclusion & Equal Employment Opportunity at Banyan: Banyan affirms that inequality is detrimental to our Global Teams, associates, our Operating Companies, and the communities we serve. As a collective, our goal is to impact lasting change through our actions. Together, we unite for equality and equity. Banyan is committed to equal employment opportunities regardless of any protected characteristic, including race, color, genetic information, creed, national origin, religion, sex, affectional or sexual orientation, gender identity or expression, lawful alien status, ancestry, age, marital status, or protected veteran status and will not discriminate against anyone on the basis of a disability. We support an inclusive workplace where associates excel based on personal merit, qualifications, experience, ability, and job performance. Recruitment Notice Banyan Software may use artificial intelligence (AI) tools to assist in screening and/or assessing applicants during the recruitment process. All hiring decisions are made by our team. Personal information submitted through your application will be collected and used for recruitment purposes in accordance with applicable privacy laws. Contact us at any time with questions about our process or to request accommodation. Beware of Recruitment Scams We have been made aware of individuals fraudulently posing as members of our Talent Acquisition team and extending fake job offers. These scams may involve requests for personal information or payment for equipment. Protect yourself by following these steps: Verify that all communications from our recruiting team come from an @banyansoftware.com email address. Remember, employers will never request payment or banking information during the hiring process. If you receive a suspicious message, do not respond — instead, forward it to careers@banyansoftware.com and/or report it to the platform where you received it. Your safety and security are important to us. Thank you for staying vigilant.", "summaryDescription" : "Director of Digital Customer Experience & AI at Banyan Software", "postedDate" : "2026-06-16T01:21:40.493", "createdAt" : "2026-06-16T01:21:40.493", "lastUpdated" : "2026-06-16T14:47:56.860", "ingestTimestamp" : "2026-06-16T01:21:40.493", "mongoId" : "6a30867df292fd229c080c3d", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 200000, "salaryAnnualMax" : 300000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "sales", "jobSubcategory" : "customer_success", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "daysOld" : 0, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "SaaS", "llmIndustryConfidence" : 0.95 }, { "id" : "6a3055d9f292fd229cf223cb", "title" : "Staff Software Engineer (AI Agents)", "company" : "Traba", "industry" : "EPD", "salary" : { "min" : 240000.0, "max" : 300000.0, "currency" : "USD", "frequency" : "Yearly" }, "location" : "New York City, NY", "locations" : [ "New York City, NY", "San Francisco" ], "timestamp" : "2026-06-16T12:09:20.778", "fingerprint" : "5655fd5027e3b9f356ce06bf3297205ef49b51c83d04d7366900017b1fc49688", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/traba/d135ea08-ce5f-4e9d-a0b8-43486fa3775e/application", "externalId" : "d135ea08-ce5f-4e9d-a0b8-43486fa3775e", "industryFunction" : { }, "structuredLocations" : [ { "city" : "New York City", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.7127281,-74.0060152" } ], "locationText" : "New York City, New York, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "remoteFriendly" : true, "rawDescription" : "Traba is the AI operating layer for the industrial supply chain. We started in workforce—temp staffing, the biggest operational pain point for the manufacturing and logistics customers we serve—and used it to embed ourselves inside their daily operations and create a far better customer experience through technology. Now those same customers are pulling us beyond staffing into the broader operational workflows that run their facilities. That foundation gave us proprietary data from millions of shifts and deep enterprise relationships. But our edge is more than data: by connecting to the systems running across every facility and activating the workers already on our platform to execute against them, we are building applied AI that drives real productivity gains and transforms how the global supply chain operates at scale. We are backed by Founders Fund, Khosla Ventures, and General Catalyst. We are seeking an entrepreneurial Staff Applied Agent Engineer to join as a founding member of the Agents team and lead the development of Traba's agentic platform—the layer that synthesizes the data flowing through our marketplace, talks to our customers' operational systems, and acts autonomously inside the workflows that run their facilities. You'll partner with our CTO to make the core architectural calls on how agents are built, evaluated, and deployed at Traba; set the bar for quality and reliability; and bring the outside perspective on agent-building, FDE-style customer immersion, and data-product craft that this 0-to-1 product needs. ABOUT YOU - You've already built agents that survived contact with reality. You've shipped agent systems into production at meaningful scale—designed the harness, picked the orchestration patterns, owned the evals, and lived with the on-call. You have strong opinions on where to draw the line between prompting, fine-tuning, retrieval, and code, and why. - Domain depth meets technical breadth. You're as comfortable in a warehouse on a customer site as you are in a design doc. You learn an industry's actual operations—WMS quirks, shift cadence, exception handling—and let that knowledge shape architecture decisions. Ideal: prior experience at a vertical AI or AI-agent company (Nash, HappyRobot, Augment, Pallet, Harvey, Legora, ElevenLabs), Palantir/Scale-style FDE, or an AI-native data company (Hex, Omni, dbt). - Set direction by shipping. You raise the engineering bar by writing the canonical example, not just the doc. You pick the foundational tools, integrate the right model providers, design the eval infrastructure—and you bring others along. - Sweat the small stuff at staff scale. You have strong opinions on design patterns, eval datasets, prompt versioning, observability for agents, and the difference between a clean abstraction and an over-engineered one. You understand that how we do one thing is how we do everything. YOU WILL - Architect Traba's agent platform end-to-end—the orchestration runtime, the eval and observability stack, the integration layer to internal services and customer systems (WMS/TMS/ERP), and the patterns that every agent we ship is built on. - Own the foundational technical decisions for this part of the business: model strategy, agent harness design, retrieval and memory architecture, tool/MCP surface, and how we measure quality. - Spend real time in the field with customers and operators. Translate what you see into durable product and codify repeatable deployment patterns so each rollout compounds on the last. - Build evaluation as a real engineering discipline—datasets, graders, regression suites, experimentation tooling—so we ship agent improvements with the same confidence we'd ship backend code. - Hire and mentor the engineers who will build alongside you. Set the technical standards that define what “good” looks like for applied AI at Traba. - Partner with the CTO, product, and ops leadership on the multi-year platform roadmap. Think ahead to what the company and the agent layer will need a year or two from now, and start building it today. YOU HAVE - 7+ years of professional software engineering experience, with 2+ years of hands-on production work on LLM- or agent-based systems. - Deep proficiency in Python and/or TypeScript/Node.js, and a strong track record designing distributed systems, APIs, and data models on PostgreSQL and modern messaging (Kafka, RabbitMQ, or equivalent). - Demonstrated ownership of a non-trivial production agent system: orchestration, tool use, retrieval, evals, observability, cost/latency tuning, and the operational lessons that come with all of it. - Background that maps to at least one of: vertical AI / AI-agent company, Palantir/Scale-style FDE, or an AI-native data company (Hex, Omni, dbt). Bonus for supply chain, logistics, or industrial operations exposure. - A history of leading 0-to-1 product builds in early-stage environments—comfortable with ambiguity, pragmatic about tradeoffs, and high-agency by default. - Strong written and verbal communication. You can run a customer workshop, write the design doc, and recruit your future teammates—often in the same week. - A genuine excitement about industrial operations and the chance to use applied AI to make them dramatically better. BENEFITS - \uD83D\uDCC8 Start-up equity - \uD83D\uDCB0 Competitive Salary - \uD83E\uDE7A 100% Paid health, dental & vision coverage - \uD83C\uDF7D️ Dinner Provided via DoorDash, free DashPass & stocked kitchen for NY employees - \uD83D\uDE8D Commuter benefit - \uD83C\uDFCB\uD83C\uDFFD Gympass Benefit - ✚✚ Additional: One Medical Membership, Gympass, HSA via Optum, Talkspace, HealthAdvocate, Teledoc Health SALARY RANGE DETAILS The compensation range for this position is set between $240,000 and $300,000, reflecting our market analysis and other relevant considerations. However, exceptions may be made for candidates with qualifications that significantly differ from those outlined in the job description. EQUAL OPPORTUNITY EMPLOYER Traba is dedicated to promoting Equal Opportunity employment practices. We evaluate all applicants without discrimination based on race, color, religion, creed, national origin, age, sex, gender, marital status, sexual orientation and identity, genetic information, veteran status, citizenship, or any other characteristics that are legally protected by local, state, or federal regulations. We encourage applicants from a variety of backgrounds, experiences, and skill sets. OUR VALUES Dream Big - We are on a path to change the world for the better. We create and communicate a bold direction that inspires a life-changing vision. We don’t sacrifice long-term value for short-term results. Olympian’s Work Ethic - Changing the world never comes easy. We work harder, longer, and smarter, not just two out of three. We put everything we have on the field. Growth Mindset - We confront the toughest challenges head-on and persevere. Sometimes we fail, but we brush ourselves off, adapt, learn, and push forward with resilience. Customer Obsession - We go the extra mile for our workers and businesses. We remain focused on delivering high-quality products and services that solve this massive and overlooked industries’ problems WHAT IS LIGHT INDUSTRIAL LABOR? Light industrial flexible staffing is a $50B labor market that encompasses entry-level jobs in warehouses & distribution centers. These workers pack boxes, load trucks, and manage warehouse operations to keep supply chains running at peak efficiency. 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Cross-functional teams", "projectManagementSkills" : [ "Program management" ], "domainKnowledge" : "Medical device software regulations; EU MDR; QSR; ISO standards; EN standards", "domainList" : [ "medical-device-software-regulations", "eu-mdr", "qsr", "iso-standards", "en-standards" ], "domainSpecificKnowledge" : [ "Medical device software regulations", "EU MDR", "QSR", "ISO standards", "EN standards" ], "communicationSkills" : "Verbal communication; Written communication", "documentationSkills" : "Regulatory filings", "continuousLearning" : "Tuition reimbursement; Student debt program; Education benefit", "problemSolvingSkills" : "Problem-solving skills; Investigate and solve problems", "specialRequirements" : "10% travel", "qualificationsBasic" : "Bachelor's Degree in related field, Minimum 9 years related work experience", "qualificationsPreferred" : "Master's degree, Submission / registration types and requirements, Experience with Class III implantable devices, Experience managing and leading a team, Certification is a plus, Working knowledge of QSR, ISO, and EN standards, Working knowledge of regulatory requirements for US, EU (EU MDR), and other international geographies, Experience with medical device software requirements and software regulations", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries. ## **JOB DESCRIPTION:** **Working at Abbott** At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to: * Career development with an international company where you can grow the career you dream of * Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. * An excellent retirement savings plan with high employer contribution * Tuition reimbursement, the [Freedom 2 Save](https://www.abbott.com/corpnewsroom/strategy-and-strength/tackling-student-debt-for-our-employees.html) student debt program and [FreeU](https://www.abbott.com/corpnewsroom/strategy-and-strength/college-degree-for-free-its-possible-with-freeu.html) education benefit - an affordable and convenient path to getting a bachelor’s degree * A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune * A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists **The Opportunity** Personalized healthcare is the future. Working on Lingo, you will help build a next-generation technology that enables individuals to make decisions about how to improve energy, lose weight or enhance athletic performance. The Lingo team embodies a start-up culture and mindset with the backing of Abbott, a company with a rich history of healthcare innovation. Join us and grow your career as you help Abbott shape the future of healthcare. We are recruiting for a **Senior** **Regulatory Affairs Manager** to join our team on-site in Alameda, CA. In this role, you will combine knowledge of scientific, regulatory and business issues to enable products to meet required legislation. Additionally, will be responsible for compiling regulatory submissions and ensure data is effectively presented for the registration of products worldwide. **What You’ll Work On** * Recruits, coaches and develops organizational talent. * Fosters a diverse workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives. * Creates an entrepreneurial environment. * Provides direction and guidance to exempt specialists and/or supervisory staff who exercise significant latitude and independence in their assignments. * May manage and coach a team of regulatory employees. * Keeps the organization's vision and values at the forefront of decision making and action. * Demonstrates effective change leadership. * Builds strategic partnerships to further departmental and organizational objectives. * Develops and executes organizational and operational policies that affect one or more groups by utilizing technical/professional knowledge and skills. * Monitors compliance with company policies and procedures (e.g. compliance with FDA, BSI, EEO regulations, etc.). * Makes decisions regarding work processes or operational plans and schedules in order to achieve department objectives. * Develops, monitors and appropriately adjusts the annual budget for department(s). * Develop regulatory strategies, approval schedules, and submission standards to achieve departmental and organizational objectives. * Assess proposed regulations and communicate new requirements to the organization. * Lead the RA process for Review and analyze labeling, advertising and promotional materials while working with Marketing teams to provide regulatory strategy and compliance input. * Assist with promotional content development and review for compliance before distribution. * Lead Regulatory Affairs Ad & Promo SOP development and review. **Required****Qualifications** * Bachelor’s Degree in a related field or an equivalent combination of education and experience * Minimum 9 years related work experience. * Provides direction and monitors progress of exempt specialists and/or supervisory staff toward departmental goals. * Monitors costs of projects and of human and material resources within a department or unit. * Monitors company-wide indicators such as market share and profitability. * Monitors external environment in area of technical or professional responsibility. * Develops and/or identifies new work processes and the improved utilization of human and material resources within the assigned or related functions or groups. * Facilitates others' participation in the continuous improvement program. * Investigates and solves problems that impact work processes and personnel within or across units or departments. * Develops and communicates a vision for the organizational unit assigned. **Preferred** **Qualifications** * Master’s degree * Submission / registration types and requirements * Experience working with Class III implantable devices. * Effective verbal and written communication with diverse audience and team. * Analytical thinking with good problem-solving skills. * Experience managing and leading a team. * Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society). * Must be able to lead and manage multiple and competing priorities and manage programs. * Working knowledge of QSR, ISO, and EN standards. Strong working knowledge of regulatory requirements for US, EU (EU MDR), and other international geographies. * Experience with medical device software requirements and software regulations. * Ability to identify risk areas and escalate issues as appropriate. [**Apply Now**](https://www.jobs.abbott/us/en) **Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:**[www.abbottbenefits.com](http://www.abbottbenefits.com/pages/candidate.aspx) Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at [www.abbott.com](http://www.abbott.com/), on Facebook at [www.facebook.com/Abbott](http://www.facebook.com/Abbott) and on Twitter @AbbottNews.Connect with us at [www.abbott.com](http://www.abbott.com/), on Facebook at [www.facebook.com/Abbott](http://www.facebook.com/Abbott) and on Twitter @AbbottNews and @AbbottGlobal. **The base pay for this position is** $130,700.00 – $261,300.00 In specific locations, the pay range may vary from the range posted. ## **JOB FAMILY:** Regulatory Operations ## **DIVISION:** LNGO Lingo ## **LOCATION:** United States > Alameda : 2601 Harbor Bay Parkway ## **ADDITIONAL LOCATIONS:** ## **WORK SHIFT:** Standard ## **TRAVEL:** Yes, 10 % of the Time ## **MEDICAL SURVEILLANCE:** No ## **SIGNIFICANT WORK ACTIVITIES:** Awkward/forceful/repetitive (arms above shoulder, bent wrists), Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day) Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans. 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Partner with product leadership; Partner with clinical stakeholders; Cross-functional teams", "projectManagementSkills" : [ "Roadmap planning" ], "domainKnowledge" : "Autism therapy; Virtual ABA therapy; Distributed systems; Data pipeline architectures; ETL pipelines; AI/LLM integration; Data-intensive systems; ML/AI systems; Model lifecycle management; Healthcare data environments; Regulated data environments; HIPAA compliance; PHI handling; Event-driven architectures; Message queues; Streaming pipelines", "domainList" : [ "autism-therapy", "virtual-aba-therapy", "distributed-systems", "data-pipeline-architectures", "etl-pipelines", "ai-llm-integration", "data-intensive-systems", "ml-ai-systems", "model-lifecycle-management", "healthcare-data-environments", "regulated-data-environments", "hipaa-compliance", "phi-handling", "event-driven-architectures", "message-queues", "streaming-pipelines" ], "domainSpecificKnowledge" : [ "Autism therapy", "Virtual ABA therapy", "Distributed systems", "Data pipeline architectures", "ETL pipelines", "AI/LLM integration", "Data-intensive systems", "ML/AI systems", "Model lifecycle management", "Healthcare data environments", "Regulated data environments", "HIPAA compliance", "PHI handling", "Event-driven architectures", "Message queues", "Streaming pipelines" ], "toolProficiency" : [ "Node.js/Express", "Postgres", "AWS ECS", "AWS RDS", "AWS S3", "AWS Lambda" ], "communicationSkills" : "Architecture docs; Design reviews; Brief executives", "documentationSkills" : "Architecture decision records", "problemSolvingSkills" : "Root cause analysis", "qualificationsBasic" : "8+ years software engineering experience, 3+ years senior/staff level role, Deep expertise in JavaScript, Deep expertise in TypeScript, Production full-stack environment experience, Command of React, Command of Node.js/Express, Command of Postgres, Experience designing distributed systems, Experience owning distributed systems, Experience designing data pipeline architectures, Experience owning data pipeline architectures, Track record of technical mentorship, Excellent written communication, Excellent verbal communication, Experience in growth-stage startup", "qualificationsPreferred" : "AWS ECS experience valued, AWS RDS experience valued, AWS S3 experience valued, AWS Lambda experience valued, Familiarity with ETL pipelines, Familiarity with AI/LLM integration patterns, Familiarity with data-intensive systems, Experience with healthcare environments, Experience with regulated data environments, HIPAA compliance experience, PHI handling experience, Familiarity with event-driven architectures, Familiarity with message queues, Familiarity with streaming pipelines, Prior experience as engineering manager, Contributions to open source, Engineering blog posts contributions, Conference talks contributions", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Staff Engineer AI/ML Remote, Anywhere in the US About AnswersNow At AnswersNow, we are trailblazing the future of autism therapy, making it more immediate, accessible, and effective for families everywhere. Our innovative virtual ABA therapy platform is thoughtfully designed by clinicians to recreate the focused, supportive environment of in-person therapy, complete with distraction-free features and interactive activities that enhance engagement and progress. Our team operates fully remote—meaning you’ll have the flexibility to work from the comfort of home. If you're ready to make a meaningful impact and join a team that's reshaping autism therapy, we’d love to hear from you! Why this role matters: We're looking for a Senior Engineering Manager who knows that great engineering leadership is about growing people, removing obstacles, and making the team better — not writing the most code. You've led teams before. You know how to hold a high bar for craft while keeping engineers energized and growing. You understand that a team of four highly effective engineers with strong habits will outperform a team of twelve with unclear expectations. You'll manage a team of Engineering Team Leads, each of whom runs a squad of full-stack engineers. You own the health of the engineering organization: hiring, performance, culture, delivery, and the processes that keep everything running. You partner closely with the CTO, product leadership, and clinical stakeholders to ensure engineering is building the right things, the right way. This is a player-coach role in spirit — you should be technically credible and able to engage meaningfully in architecture discussions — but your primary output is team output, not individual code. Job Details - W2 Employee - Full-Time - 100% Remote Job Requirements - 8+ years of professional software engineering experience, with at least 3 years in a senior or staff-level role - Deep expertise in JavaScript and TypeScript in a production full-stack environment - Strong command of React, Node.js/Express, and Postgres — you can reason about performance, reliability, and maintainability at each layer - Proven experience designing and owning distributed systems or data pipeline architectures on AWS (ECS, RDS, S3, Lambda experience valued) - Track record of technical mentorship — you've made engineers around you measurably better - Excellent written and verbal communication; you can write an architecture doc, run a design review, and brief a non-technical executive in the same day - Experience working in or leading engineering at a growth-stage startup — you understand the balance between velocity and sustainability - Familiarity with ETL pipelines, AI/LLM integration patterns, or data-intensive systems is a strong plus - Significant experience architecting and deploying production-grade ML/AI systems, including LLM integration and model lifecycle management. Nice to have: - Experience with healthcare or regulated data environments (HIPAA compliance, PHI handling) - Familiarity with event-driven architectures, message queues, or streaming pipelines - Prior experience as an engineering manager who returned to an IC track (player-coach background welcome) - Contributions to open source or engineering blog posts / conference talks What You’ll Do Technical Leadership - Own and evolve the architecture of our core platform: React frontend, Node.js/Express APIs, Postgres, and AWS ECS infrastructure - Drive our JavaScript → TypeScript migration, establishing patterns, tooling, and standards the team can follow - Design and extend our ETL pipeline and config-driven AI integration framework, enabling engineers to ship AI-powered features faster and more reliably - Lead technical design reviews, create architecture decision records (ADRs), and ensure engineering decisions are documented and defensible - Identify and resolve systemic technical debt — not just flagging it, but owning the plan to address it - Define and execute the technical strategy for integrating ML/AI models into our core platform, ensuring scalability, performance, and reliability. Engineering Culture & Mentorship - Mentor engineers across all levels — pair, review, coach, and grow the team's collective capability - Establish and maintain engineering standards: code quality, testing practices, observability, on-call runbooks, and incident response - Serve as a technical resource and thought partner for product, clinical, and business stakeholders - Help define the engineering hiring bar and participate in the interview process Delivery & Operations - Partner with engineering leadership and product to scope, sequence, and de-risk large technical initiatives - Lead by example on production support — define runbooks, own post-mortems, and drive systemic fixes from incidents - Work across UI, API, DB, and infrastructure layers with genuine depth in at least two What we Offer - $151,000- $178,500 annual salary - Fully remote – work from anywhere in the U.S. - Flexible hours with an async-friendly team culture More About AnswersNow AnswersNow welcomes applicants of all backgrounds, experiences, and abilities. We believe a diverse team is a strong team, and are committed to provide a fair and equitable experience for every candidate. If you require reasonable accommodations at any stage, we encourage you to reach out. We’re here to support! Learn more about us at getanswersnow.com http://getanswersnow.com.", "summaryDescription" : "Staff Engineer AI/ML at AnswersNow. Skills: AI/ML, Full-stack development, Distributed systems, Data pipelines. Own platform architecture. Evolve platform architecture", "createdAt" : "2026-06-14T18:40:37.087", "lastUpdated" : "2026-06-16T01:55:30.858", "ingestTimestamp" : "2026-06-14T18:40:37.087", "mongoId" : "6a2cd5f974d8ee00a0a3c9c4", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 150000, "salaryAnnualMax" : 215000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Full-stack development", "Data pipeline architecture", "ML/AI system architecture", "Model lifecycle management", "Leadership", "AI/ML", "Distributed systems", "Data pipelines", "System design", "Technical mentorship", "Architecture discussions", "Technical strategy", "Production support", "Incident response", "Roadmap planning", "Autism therapy", "Virtual ABA therapy", "Data pipeline architectures", "ETL pipelines", "AI/LLM integration", "Data-intensive systems", "ML/AI systems", "Healthcare data environments", "Regulated data environments", "HIPAA compliance", "PHI handling", "Event-driven architectures", "Message queues", "Streaming pipelines", "Node.js/Express", "Postgres", "AWS ECS", "AWS RDS", "AWS S3", "AWS Lambda" ], "skillCount" : 35, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Executive", "dataQualityScore" : 0.8888889, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c927574d8ee00a0985dc2", "title" : "Staff Engineer, AI Productivity", "company" : "Hightouch", "industry" : "Technology", "salary" : { "min" : 225000.0, "max" : 325000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Lead Staff Engineer in the Technology industry in New York, adjusted for seniority and company size." }, "location" : "New York, New York, United States", "locations" : [ "New York", "New York", "United States", "San Francisco", "California", "United States" ], "timestamp" : "2026-06-16T05:10:47.727", "fingerprint" : "b045e963c70bdff7b328000bc68b4fe1108d0b62fe854c1a8e338bf38e4d8291", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/hightouch/jobs/6020404004", "externalId" : "6020404004", "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", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "TypeScript, JavaScript, Go, GraphQL, CI/CD, Cloud infrastructure, Internal tooling, Application code", "professionalSkills" : [ "System design", "Developer tools", "Infrastructure" ], "hardSkillsList" : [ "Agent documentation", "Custom instructions", "Context files" ], "hardSkills" : [ { "name" : "Agent documentation", "level" : "intermediate" }, { "name" : "Custom instructions", "level" : "intermediate" }, { "name" : "Context files", "level" : "intermediate" } ], "majorSkills" : "AI Productivity, Developer Experience, Agentic Development", "majorSkillsList" : [ "AI Productivity", "Developer Experience", "Agentic Development" ], "coreResponsibilities" : "Own agentic development environment, Build tooling integrations, Connect agents to systems, Create documentation and context, Expose conventions and package structures, Enable engineers with better docs, Develop tooling for non-engineers, Make visual updates to application, Serve as PM for AI agents, Keep abreast of AI trends, Drive improvements across Hightouch", "teamCollaboration" : "Cross-team efforts; Work with teams", "domainKnowledge" : "AI coding tools; Agent development; Cloud development environments; Internal systems; Software development; AI productivity trends; State-of-the-art AI", "domainList" : [ "ai-coding-tools", "agent-development", "cloud-development-environments", "internal-systems", "software-development", "ai-productivity-trends", "state-of-the-art-ai" ], "domainSpecificKnowledge" : [ "AI coding tools", "Agent development", "Cloud development environments", "Internal systems", "Software development", "AI productivity trends", "State-of-the-art AI" ], "toolProficiency" : [ "CircleCI", "Slack", "Datadog", "Github", "Claude Code", "Cursor", "Copilot", "Devin" ], "documentationSkills" : "Agent guidance; Agent skills", "problemSolvingSkills" : "Root cause analysis", "qualificationsBasic" : "Deep hands-on experience with AI coding agents, Experience writing effective agent documentation, Track record of building developer tools, Comfortable working across the stack", "qualificationsPreferred" : "Experience building MCP servers, Background in developer productivity, Experience with TypeScript/JavaScript monorepos, Experience with Go, Experience with GraphQL, Set up sandboxed development environments at scale, Containerized development environments at scale", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "About Hightouch Hightouch is an Agentic Marketing Platform powered by the industry-leading Composable CDP. With complete brand context, customer data, and performance history in one place, every marketer finally has the power to build and ship end-to-end campaigns themselves. Teams move faster, stay on brand, and get AI marketing that actually works. Founded in 2019 and headquartered in San Francisco, Hightouch enables marketing teams to analyze performance, brainstorm ideas, and generate creative at a speed and quality that wasn't previously possible. Named a Leader in the 2026 Gartner® Magic Quadrant™ for Customer Data Platforms, Hightouch is trusted by leading enterprises like Domino's, Spotify, Aritzia, Cars.com, Ramp, and PetSmart. At Hightouch, our mission is to help our customers leverage data and AI to grow their businesses. The team is ambitious, impact-driven, efficient — and we believe humility, kindness, and compassion are essential to our success. If you're energized by velocity, obsessed with raising the bar, and want to build alongside people who care deeply about each other and our customers, we'd love to meet you. About the Role We are looking for a Staff AI Productivity Engineer to accelerate how our engineering organization works with AI coding tools. This is a hands-on technical role focused on building infrastructure, tooling, and documentation that makes AI agents dramatically more effective across our codebase. AI tools are evolving rapidly, and we believe the companies that invest in making agents truly productive - not just available - will have a significant advantage. You'll own this problem end-to-end: from setting up cloud development environments where agents can run autonomously, to building MCP integrations that give agents access to our internal systems, to creating the documentation and context that helps agents understand how we build software. You’ll have the hands-on acumen to do a lot of the heavy lifting yourself and the leadership skills to drive cross-team efforts to raise the bar everywhere. This role is a companion role to our Developer Productivity role but has a distinct focus: while Dev Productivity owns the build/test/deploy pipeline, you'll own the AI-assisted development experience. An exceptional candidate could wear both hats. Some of the problems we’ll be working on include: Own the agentic development environment: Ensure agents can operate in independent cloud-based development environments, execute our full test suites, examine build results visually, etc Build our tooling integrations: Build MCP server integrations that connect our agents to the systems needed to build and debug software, such as CircleCI, Slack, Datadog, Github, etc Documentation and context: Own our repo-wide agents.md file and work with teams to ensure our library of agent guidance and skills is continually pushing the bar. Ensure our conventions and package structures are exposed in ways that agents can effectively use Enablement: Work with our engineers to understand where agents are struggling and address root causes such as better docs, tooling access, etc. Develop tooling for non-engineers to make simple visual updates to our application Serve as a “PM” for internal AI agents: Consistently keep us on the leading edge of AI productivity trends by staying abreast of what is state-of-the-art in industry and driving those improvements across Hightouch We are looking for talented, intellectually curious, and motivated individuals who are interested in tackling the problems above. This is a senior role, but we focus on impact and potential for growth more than years of experience. The salary range for this position is $180,000 - $400,000 USD per year, which is location independent in accordance with our remote-first policy. We also offer meaningful equity compensation in the form of ISO options, and offer early exercise and a 10 year post-termination exercise window. About You You are an engineer with a passion for solving hard technical problems that generate real value for customers. You’re motivated by high ownership and are comfortable in a fast-paced, startup environment. Must have Strong software engineering fundamentals—you can dive into complex backend code and understand it quickly Deep hands-on experience with AI coding agents (Claude Code, Cursor, Copilot, Devin, or similar) Experience writing effective agent documentation, custom instructions, or context files that meaningfully improved agent output Track record of building developer tools or infrastructure that other engineers actually use Comfortable working across the stack: you'll touch CI/CD, cloud infrastructure, internal tooling, and application code Nice to have Experience building or contributing to MCP servers or similar agent-tooling integrations Background in developer productivity, platform engineering, or developer experience roles Experience with our stack: TypeScript/JavaScript monorepos, Go, GraphQL You've set up sandboxed or containerized development environments at scale Interview Process Our goal with the interview process is to balance speed with giving both parties opportunities to assess whether there is a strong mutual fit. We will ask you questions, but we want you to ask us questions! Our technical interviews focus on how you design systems because we believe this is the best way for us to see how you work and for you to see how we collaborate. We don’t ask you to write code to solve technical brainteasers that don’t appear in your day to day job. Apply: Curl jobapi.hightouchdata.com on port 13784 and have followed those instructions before applying. It'll only take a minute! Recruiter Screen [30m]: Introductory call with our recruiting team to get to know each other and see if the role could be a good mutual fit System Design Screen [45m]: Designing a data processing feature end-to-end AI Skills Interview [60m]: We’ll dive into how you leverage AI and how you’ve helped others do the same Hiring Manager Interview [45m]: Chat with hiring manager about past experiences and future operating preferences to assess fit on company values and operating principles System Design Interview [90m]: Work with the interviewer to architect a system at a conceptual level. The problem will be at a pretty high level - and have both product and customer requirements as well as technical E-Verify Statement Hightouch participates in E-Verify. After you join the team, we'll verify your eligibility to work in the U. S. by submitting information from your Form I-9 to the Social Security Administration and, if needed, the Department of Homeland Security. This process happens post-hire only — we never use E-Verify to pre-screen applicants. E-Verify Notice E-Verify Notice (Spanish) Right to Work Notice Right to Work Notice (Spanish)", "summaryDescription" : "Staff Engineer, AI Productivity at Hightouch. Skills: AI Productivity, Developer Experience, Agentic Development. Own agentic development environment. Build tooling integrations", "postedDate" : "2026-06-14T18:38:12.424", "createdAt" : "2026-06-14T18:38:12.424", "lastUpdated" : "2026-06-16T05:10:47.727", "ingestTimestamp" : "2026-06-14T18:38:12.424", "mongoId" : "6a2c927574d8ee00a0985dc2", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 225000, "salaryAnnualMax" : 325000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Agent documentation", "Custom instructions", "Context files", "AI Productivity", "Developer Experience", "Agentic Development", "System design", "Developer tools", "Infrastructure", "AI coding tools", "Agent development", "Cloud development environments", "Internal systems", "Software development", "AI productivity trends", "State-of-the-art AI", "CircleCI", "Slack", "Datadog", "Github", "Claude Code", "Cursor", "Copilot", "Devin" ], "skillCount" : 24, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Lead", "dataQualityScore" : 0.8888889, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.98 }, { "id" : "6a307110f292fd229cff7b0d", "title" : "Senior Staff AI Compiler Engineer", "company" : "Renesas Electronics", "industry" : "Semiconductors", "salary" : { "min" : 195000.0, "max" : 275000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Senior Staff AI Compiler Engineer in Austin, United States, adjusted for industry and company size." }, "location" : "Austin, TX, United States", "locations" : [ "Austin", "TX", "United States" ], "timestamp" : "2026-06-16T11:28:08.741", "fingerprint" : "cc58e66e7b806690a4088f0f3ff2010c39424acd55077c88c71f066daa6884ff", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/RenesasElectronics/744000132249820-senior-staff-ai-compiler-engineer", "externalId" : "744000132249820", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Austin", "state" : "Texas", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "30.2711286,-97.7436995" } ], "locationText" : "Austin, Texas, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "MS/PhD", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "mid", "remoteFriendly" : false, "rawDescription" : "Renesas Electronics is searching for a hands-on AI Compiler Engineer who thrives at the convergence of cutting-edge AI, compiler tech, and hardware design. Here, you’ll not only architect and scale a production-class AI compiler toolchain, but also rethink how AI automates, optimizes, and accelerates every step of building and deploying neural networks on Renesas SoCs. You’ll work shoulder-to-shoulder with visionary engineers—both human and AI—enabling adaptive compilers that learn, evolve, and redefine what’s possible for embedded intelligence. With a relentless focus on hardware-software co-design, you’ll collaborate across teams to translate high-level AI models into blazing-fast, energy-efficient executables, unlocking the full potential of our silicon for real-world impact. Innovation here isn’t a catchphrase—it’s your everyday. Responsibilitiess: * Develop an AI compiler toolchain, working with AI agents to map neural networks onto Renesas SoC platforms. * Creating and testing new graph transformations, lowering, scheduling, and code generation methods for CPUs and custom accelerators, using insights from AI-powered analytics. * Work on integrating popular AI frameworks like PyTorch, TensorFlow, and ONNX, using AI agents to support new model architectures and operations more quickly. * Improve quantization, operator fusion, memory planning, and layout transformations, learning from both team members and AI-guided designs for better performance. * Collaborate with hardware and software architects, kernel developers, and AI agents to help co-design compiler and accelerator features, supporting alignment between silicon and code for greater efficiency. * Diagnose and crush performance bottlenecks with AI-enabled profiling and diagnostics, relentlessly tuning for latency, throughput, and power efficiency. * Level up validation, benchmarking, and regression pipelines by harnessing AI agents—ensuring compiler correctness and world-class performance, release after release. * Uplevel the developer experience by streamlining usability, diagnostics, and documentation—AI agents are your copilots for user support, troubleshooting, and rapid iteration. ## Qualifications * MS/PhD (or equivalent experience) in Computer Science, EE, or related field * Hands-on experience with compilers, AI systems, or high-performance software, and a genuine interest in using AI to enhance engineering productivity and drive innovation. * Comfortable coding in C/C++ and Python, able to contribute to established codebases, and open to collaborating with teammates and AI agents. * Understanding of machine learning models, computational graphs, and operator concepts, with a willingness to learn how AI can support and streamline processes. * Familier with compiler frameworks (TVM, MLIR, LLVM, etc.) or proprietary stacks, and interest in learning how to extend their features with AI-driven approaches. * General knowledge of CPU/GPU/accelerator architecture, memory systems, and optimization principles, with enthusiasm for working on hardware-software integration projects. * Creative problem-solver who enjoys tackling performance and correctness issues, including those identified by AI-powered analysis tools. * Effective communicator and team player who is comfortable collaborating in cross-functional environments with engineers and AI copilots. ## Additional Information Renesas is an embedded semiconductor solution provider driven by its Purpose ‘To Make Our Lives Easier.’ As the industry’s leading expert in embedded processing with unmatched quality and system-level know-how, we have evolved to provide scalable and comprehensive semiconductor solutions for automotive, industrial, infrastructure, and IoT industries based on the broadest product portfolio, including High Performance Computing, Embedded Processing, Analog & Connectivity, and Power. With a diverse team of over 22,000 professionals in more than 30 countries, we continue to expand our boundaries to offer enhanced user experiences through digitalization and usher into a new era of innovation. We design and develop sustainable, power-efficient solutions today that help people and communities thrive tomorrow, ‘To Make Our Lives Easier.’ At Renesas, you can: * Launch and advance your career in technical and business roles across four Product Groups and various corporate functions. You will have the opportunities to explore our hardware and software capabilities and try new things. * Make a real impact by developing innovative products and solutions to meet our global customers' evolving needs and help make people’s lives easier, safe and secure. * Maximize your performance and wellbeing in our flexible and inclusive work environment. Our people-first culture and global support system, including the remote work option and Employee Resource Groups, will help you excel from the first day. Are you ready to own your success and make your mark? Join Renesas. Shape Your Future with Us. Renesas Electronics is an equal opportunity and affirmative action employer, committed to celebrating diversity and fostering a work environment free of discrimination on the basis of sex, race, religion, national origin, gender, gender identity, gender expression, age, sexual orientation, military status, veteran status, or any other basis protected by federal, state or local law. For more information, please read our [Diversity & Inclusion Statement](https://jobs.renesas.com/diversity-and-inclusion). Renesas Electronics deals with dual-use technology that is subject to U.S. export controls regulations. Under these regulations it may be necessary for Renesas to obtain U.S. government export license prior to release of technology to certain persons. The decision whether or not to file or pursue an export license application is at the sole discretion of Renesas.", "summaryDescription" : "Senior Staff AI Compiler Engineer at Renesas Electronics", "postedDate" : "2026-06-15T17:07:10.000", "createdAt" : "2026-06-16T01:31:30.234", "lastUpdated" : "2026-06-16T11:28:08.741", "ingestTimestamp" : "2026-06-16T01:31:30.234", "mongoId" : "6a307110f292fd229cff7b0d", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 195000, "salaryAnnualMax" : 275000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 0.8888889, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.98 } ], "status" : 200, "message" : "staff regulatory affairs associate digital health ai technologies jobs", "metadata" : { "title" : "staff regulatory affairs associate digital health ai technologies" }, "pagination" : { "page" : 0, "limit" : 50, "totalCount" : 68842, "totalPages" : 1377, "hasNext" : true, "hasPrevious" : false } }

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