• GRA Device Lead ( Associate

    Sanofi Group (Morristown, NJ)
    **Job Title:** GRA Device Lead ( Associate Director ) - Digital Health **Location:** Cambridge, MA/ Morristown, NJ **About the Job** GRA Device Lead ( ... be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting the medical device ,… more
    Sanofi Group (12/19/25)
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  • Assoc Director , Patient Safety Medical…

    Gilead Sciences, Inc. (Parsippany, NJ)
    …individual to join the **Patient Safety Strategic Operations** team as an ** Associate Director , Patient Safety Medical Device Safety** responsible ... strategies and ensure operational excellence through successful business partner collaboration. The Associate Director , PS Medical Device Safety will be… more
    Gilead Sciences, Inc. (10/16/25)
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  • Assoc. Dir., Engineering , Combination Products…

    Merck (Rahway, NJ)
    …Description** Reporting into the Director Packaging Platform Technical Leadership the Associate Director Medical Device and Combination Product (MDCP) ... compliant supply of commercialized products for the benefit of patients. The Associate Director of MDCP Platform Packaging and Assembly Technical Leadership… more
    Merck (11/11/25)
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  • Associate Principal Scientist,…

    Merck (Rahway, NJ)
    **Job Description** The Associate Principal Scientist, Device Risk Management Lead, is a crucial member of our team, responsible for spearheading risk management ... concept through launch and post-market surveillance. **Key Responsibilities and Activities:** The Associate Principal Scientist, Device System - Device Risk… more
    Merck (12/13/25)
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  • Associate Director , Market Access…

    Abbott (Princeton, NJ)
    …Abbott is seeking a passionate and driven professional to join our team as ** Associate Director , Market Access and Payer Relations** , supporting the East Coast ... working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more effective, and… more
    Abbott (10/24/25)
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  • Associate Director , Inspection…

    Bristol Myers Squibb (Princeton, NJ)
    …lives. Read more: careers.bms.com/working-with-us . **Position Summary** Reporting to the Director , Inspection Readiness, the Associate Director will ... and collaborate extensively with teams and leaders across the BMS network. The Associate Director will support BMS' GMP/GDP Inspection Readiness strategy by… more
    Bristol Myers Squibb (12/21/25)
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  • Associate IT Director - Business…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    **Job Description Summary** The Associate IT Director Business Partner will report to the TGS Senior Director , Product Services and work with the Quality ... your best self. Become a **maker of possible** with us. **Position Overview** The Associate IT Director Business Partner will serve as the critical link between… more
    BD (Becton, Dickinson and Company) (11/12/25)
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  • Associate Director , Logistics…

    Merck (Rahway, NJ)
    …Reporting into the Director , Logistics and Distribution Technology the Associate Director , Logistics and Distribution Technology will be responsible and ... to shape the technical capabilities lead a global, cross-modality technical team. The Associate Director will lead a team of technical experts responsible… more
    Merck (10/16/25)
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  • Regulatory Affairs Associate

    GRAIL (Trenton, NJ)
    …position supports the US Regulatory team in preparing Investigational Device Exemptions (IDEs), IDE supplements, pre-submissions, Premarket Approvals (PMAs), annual ... 510(k)s, post-approval reports, annual reports, export certificates, establishment registrations, and device listings. + Serve as a key member of the Regulatory… more
    GRAIL (12/03/25)
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  • Associate Director , Regulatory…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the ... JPMA, etc.). + Demonstrate solid working knowledge of the drug, biologic, and device development process, laws, regulations, and guidelines from FDA, EMA, PMDA, ICH,… more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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