• Medical Device Regulatory

    Oracle (Boston, MA)
    …driving Oracle's success and competitiveness in the healthcare and life sciences sector. As a Medical Device Regulatory Affairs Strategist, you will work ... with SaMD in areas such as Regulatory Affairs , Quality Compliance, Product Development, etc. in medical... Affairs , Quality Compliance, Product Development, etc. in medical device industry or equivalent. Experience authoring… more
    Oracle (11/25/25)
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  • Director, US Regulatory Affairs

    Sanofi Group (Cambridge, MA)
    …Sciences or other relevant discipline + 8+ years of experience within pharmaceutical or medical device Regulatory Affairs , with 5+ years specifically ... **Job Title:** Director, US Regulatory Affairs - Advertising and Promotion...without relying on authority, including participating in cross-functional groups ( medical , legal, regulatory , etc.) to lead toward… more
    Sanofi Group (10/23/25)
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  • Regulatory & Market Access Intern x2

    Avania (Boston, MA)
    …are Hiring - Regulatory & Market Access Interns x2 We are seeking two, part-time Medical Device Regulatory Affairs & Quality Interns to join the ... efforts. + Content Development + Contribute to creation of medical device regulatory and quality-focused...Northeastern University Master of Science in Regulatory Affairs students with interest in medical devices.… more
    Avania (10/22/25)
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  • Global Regulatory Affairs

    Sanofi Group (Cambridge, MA)
    **Job title** : Global Regulatory Affairs Device Lead (Associate Director) **Location** : Morristown, NJ or Cambridge, MA or Framingham, MA **About the Job** ... critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team...Sanofi's regulatory framework, providing expert guidance on medical device regulatory requirements across… more
    Sanofi Group (10/23/25)
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  • Regulatory Affairs Manager

    Dentsply Sirona (Waltham, MA)
    …Years and Type of Experience: + 5(+) years of experience in regulatory affairs , preferably in the medical device industry. + Experience with leading ... + Manages day to day activities for less senior Regulatory Affairs professionals, including but not limited...13485, EU MDR). + Experience with software as a medical device , AI and/or medical more
    Dentsply Sirona (09/18/25)
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  • Senior Regulatory Affairs Specialist

    Medtronic (Boston, MA)
    …Have: Minimum Requirements** + Bachelors degree with 4+ years of regulatory affairs experience in the medical device , biotech or pharmaceutical industry ... OR a Masters degree with 2+ years of regulatory affairs experience in the medical device , biotech or pharmaceutical industry. **Nice to Have** +… more
    Medtronic (11/18/25)
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  • Principal Regulatory Affairs

    Philips (Cambridge, MA)
    …if:** + You've acquired a minimum of 7+ years' experience in Regulatory Affairs /Strategy within FDA regulated Medical Device environments. + You have ... The Principal Regulatory Affairs Specialist will develop and...The Principal Regulatory Affairs Specialist will develop and execute the ...corrections, with a primary focus on Software as a Medical Device (SaMD) for our Sleep &… more
    Philips (11/11/25)
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  • Senior Principal Regulatory Affairs

    Bausch + Lomb (Boston, MA)
    …+ Minimum of 8 years in recent experience in strategic pharmacuetical Regulatory Affairs . This position does not work with medical device , cosmetics or ... and ability to see the business drivers outside of Regulatory Affairs + Ability to take innovative...**We offer competitive salary & excellent benefits including:** + Medical , Dental, Eye Health, Disability and Life Insurance begins… more
    Bausch + Lomb (09/06/25)
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  • Sr. Manager, Regulatory Affairs Cell…

    ThermoFisher Scientific (Waltham, MA)
    …or helping find cures for cancer. **Discover Impactful Work** As a Sr. Manager, Regulatory Affairs , you will play a crucial role in interpreting and ... requirements and desired marketing claims. + Author and/or review regulatory submissions, specifically device master files, ...count on, which includes: + A choice of national medical and dental plans, and a national vision plan,… more
    ThermoFisher Scientific (11/08/25)
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  • Manager, Medical Affairs Strategy

    IQVIA (Boston, MA)
    …data, etc.), HCP engagement by life sciences companies. Expertise in domains adjacent to medical affairs , such as regulatory or pharmacovigilance, would also ... **Manager, Medical Affairs Strategy** **Overview** IQVIA is...diverse client base includes the global top 20 pharmaceutical, medical device , and biotechnology companies as well… more
    IQVIA (11/04/25)
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  • Global Medical Affairs Director…

    Sanofi Group (Cambridge, MA)
    **Job Title:** Global Medical Affairs Director - Oncology **Location:** Cambridge, MA / Morristown, NJ **About the job** **About us:** In order to pursue ... miracles of science to improve people's lives", Specialty Care Medical Affairs have a vision to be...engagement. We serve as key strategic partners for commercial, regulatory , R&D, market access and external affairs more
    Sanofi Group (10/02/25)
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  • Senior Counsel ( Medical Device )

    Fujifilm (Boston, MA)
    …**Job Description** **Responsibilities** + Manage and support the day-to-day legal affairs of assigned Medical Device businesses or ... Counsel and senior business management on general legal and regulatory risks affecting the Medical Device businesses, including with respect to healthcare… more
    Fujifilm (09/04/25)
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  • GRA Device Associate

    Sanofi Group (Cambridge, MA)
    …strategic partner within Sanofi's regulatory framework, providing expert guidance on medical device regulatory requirements across the product lifecycle. ... critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team...teams. + Contribute to and execute innovative and sustainable medical device regulatory strategies covering… more
    Sanofi Group (09/20/25)
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  • Head Global Quality Device Compliance…

    Takeda Pharmaceuticals (Lexington, MA)
    …councils, inspection support, and industry interactions. + Partner with critical stakeholders in Regulatory Affairs , Device Quality, and PharmSci to ensure ... medical devices, including stand-alone devices, combination devices, and Software as a Medical Device (SaMD). You will ensure that Quality System requirements… more
    Takeda Pharmaceuticals (11/26/25)
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  • Associate Director, Device Clinical…

    Takeda Pharmaceuticals (Lexington, MA)
    …and device development teams + Serve as clinical liaison to Global Device Team, including engineering, regulatory affairs , quality, and commercial ... degree with 15+ years of experience** + Minimum 5 years of combination product, medical device , or pharmaceutical industry experience + Experience with both … more
    Takeda Pharmaceuticals (09/04/25)
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  • Vice President, Internal Medicine…

    Pfizer (Cambridge, MA)
    …industry, preferably in Drug Development or Clinical Research, ideally within Regulatory Affairs + Subject-matter expertise within assigned therapeutic area ... to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned. Regulatory Affairs more
    Pfizer (11/13/25)
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  • Associate Director, Regulatory Intelligence

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …development programs. + Build professional network with key stakeholders outside of Global Regulatory Affairs to identify regulatory intelligence needs and ... in a scientific or technical discipline preferred. + Minimum of 5 years of regulatory affairs experience. + Minimum 2-3 years' work experience in regulatory more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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  • Senior Specialist, Medical Writing

    Edwards Lifesciences (Boston, MA)
    …Bachelor's Degree in a related field with 5 years of related experience working in medical affairs , clinical affairs and/or clinical science **What else we ... internal/external working relationships + The Sr. Specialist will be an experienced medical device professional with strong scientific acumen and a commitment… more
    Edwards Lifesciences (09/27/25)
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  • Medical Director, Gastrointestinal…

    Takeda Pharmaceuticals (Boston, MA)
    …and communicate safety issues with other functional areas such as Clinical Development, Regulatory Affairs , Quality Assurance, Medical Affairs , ... the Company-wide patient safety expert for assigned pharmaceutical / biological / drug- device combined products, accountable for the safety strategy and major safety… more
    Takeda Pharmaceuticals (11/23/25)
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  • CER Technical Writer

    Kelly Services (Raynham, MA)
    …in quality regulatory compliance, complaint handling, adverse event reporting, medical device risk management processes, and experience with common ... The CER Technical Writer must have experience within the medical device industry and knowledge of clinical...Directors, Post Market Surveillance, Design Quality Engineers, R&D, Clinical Affairs and Regulatory Affairs relating… more
    Kelly Services (10/03/25)
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