• Global Regulatory Affairs

    Sanofi Group (Morristown, NJ)
    **Job title** : Global Regulatory Affairs Device Lead (Associate Director) **Location** : Morristown, NJ or Cambridge, MA or Framingham, MA **About the ... could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting the… more
    Sanofi Group (10/23/25)
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  • Global Regulatory Affairs CMC…

    Sanofi Group (Morristown, NJ)
    …we chase the miracles of science to improve people's lives. The Global Regulatory Affairs (GRA) CMC & Device Organization within Sanofi R&D serves ... **Job Title:** Global Regulatory Affairs CMC...**Job Title:** Global Regulatory Affairs CMC lead **Location:** Framingham,...GRA CMC Lead within our GRA CMC & GRA Device Organization, you'll drive global regulatory more
    Sanofi Group (10/15/25)
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  • GRA Device Associate

    Sanofi Group (Morristown, NJ)
    …skills could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting ... pathways. The team is accountable for developing and implementing global regulatory strategies for device ...team creates and maintains strong collaborative working relationships with Global Regulatory Affairs (GRA), Regional… more
    Sanofi Group (09/20/25)
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  • Staff Regulatory Affairs Specialist

    embecta (Parsippany, NJ)
    …or technical discipline (eg engineering, bioengineering, biology, chemistry). + 5+ years Regulatory Affairs experience in medical device companies. + ... devices in both the US and Europe, and related regulatory affairs activities to ensure compliance with...Experience negotiating with Health Authority personnel in the medical device area. + Demonstrated global perspective, customer… more
    embecta (11/05/25)
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  • Director, Regulatory Affairs

    Bayer (Whippany, NJ)
    …technology and strategic regulatory leadership. As the Director of Regulatory Affairs , you will represent our medical device regulatory team within ... + Compliance & Policy Contribution: Actively contribute to shaping global regulatory compliance policies and procedures that...quality systems are required + Direct professional experience in Regulatory Affairs within the medical device more
    Bayer (11/08/25)
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  • Senior Regulatory Affairs Specialist

    Pentax Medical (Montvale, NJ)
    …devices and solutions to the global medical community. Position Opening: Senior Regulatory Affairs Specialist Why JOIN Us? We are an established medical ... for Endoscopes and Speech, Voice and Swallowing devices, meet global regulatory standards. This role will collaborate...shaping the future of medical technology. Responsibilities of Senior Regulatory Affairs Specialist : + Coordinate with… more
    Pentax Medical (10/24/25)
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  • Director, US Regulatory Affairs

    Sanofi Group (Morristown, NJ)
    …other relevant discipline + 8+ years of experience within pharmaceutical or medical device Regulatory Affairs , with 5+ years specifically within advertising ... **Job Title:** Director, US Regulatory Affairs - Advertising and Promotion...training and team leadership opportunities. We are an innovative global healthcare company with one purpose: to chase the… more
    Sanofi Group (10/23/25)
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  • Global Medical Affairs Director…

    Sanofi Group (Morristown, NJ)
    **Job Title:** Global Medical Affairs Director - Oncology **Location:** Cambridge, MA / Morristown, NJ **About the job** **About us:** In order to pursue ... engagement. We serve as key strategic partners for commercial, regulatory , R&D, market access and external affairs ...unmet needs. Sanofi is recruiting a new Director in Global Medical Affairs (GMA) based in Cambridge,… more
    Sanofi Group (10/02/25)
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  • Director, SM Medical Affairs , Specimen…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …Description** We are **the makers of possible** ! BD is one of the largest global medical technology companies in the world. _Advancing the world of health_ (TM) is ... possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve....directly to the business unit Vice President of Medical Affairs , the Director of Medical Affairs has… more
    BD (Becton, Dickinson and Company) (09/20/25)
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  • Medical Affairs Manager IPD

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …the core team, aiding product development, remediation projects, and meeting medical device regulatory needs. + Review, comprehend, and compose performance and ... role in crafting the future of medical technology and making a tangible impact on global health. **Responsibilities:** + Present the medical affairs role within… more
    BD (Becton, Dickinson and Company) (10/26/25)
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  • Manager, Medical Affairs Strategy

    IQVIA (Parsippany, NJ)
    **Manager, Medical Affairs Strategy** **Overview** IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services ... of innovative medical treatments. Our diverse client base includes the global top 20 pharmaceutical, medical device , and biotechnology companies… more
    IQVIA (11/04/25)
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  • Director Global Regulatory Strategy…

    Bayer (Whippany, NJ)
    global regulatory project goals from development through life cycle; + Represents Global Regulatory Affairs on assigned global Project Teams; + ... minds to make a real difference, there's only one choice.** **Director Global Regulatory Strategy (Molecular Imaging, Pharmaceuticals)** The position is… more
    Bayer (11/27/25)
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  • Senior RA Specialist

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …510(k), Q-Sub), EU technical documentation under MDR, and other global regulatory filings. + Evaluate medical device regulations and lead the development ... **Job Description Summary** The Senior Regulatory Affairs (RA) Specialist will represent...change control, ensuring compliance with US, EU, and other global regulatory requirements. + Author FDA submissions… more
    BD (Becton, Dickinson and Company) (11/14/25)
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  • Quality Specialist of Document Management

    embecta (Parsippany, NJ)
    … changes, internal audits, or process improvements. + Ensure documentation adheres to global medical device regulatory requirements, including FDA 21 CFR ... to enhance efficiency and compliance. + Collaborate with Quality, Manufacturing, Marketing, Medical Affairs , R&D, and Regulatory Affairs teams to ensure… more
    embecta (10/15/25)
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