• Associate Director , Global

    J&J Family of Companies (Raritan, NJ)
    …Johnson & Johnson Innovative Medicine R&D is recruiting for an Associate Director , Global Regulatory Affairs Diagnostics. This ... application. We invite candidates from any location to apply. The Associate Director , Global Regulatory Affairs Diagnostics will provide an opportunity… more
    J&J Family of Companies (10/28/25)
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  • Associate Director , Regulatory

    Gilead Sciences, Inc. (Parsippany, NJ)
    …of our day and improving the lives of patients for generations to come. As an Associate Director , Global Regulatory Affairs , you will act as the Regional ... Affairs and may serve as Regional Regulatory Lead or Global Regulatory ...current global and regional trends in biopharmaceutical regulatory affairs . Proven effectiveness applying this knowledge… more
    Gilead Sciences, Inc. (10/22/25)
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  • Associate Director , Regulatory

    Sumitomo Pharma (Trenton, NJ)
    Regulatory Affairs (Oncology).** The Associate Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/She will primarily ... function as a regional regulatory leader (RRL) and/or Global ...Ideally with a minimum of 4 years focused in regulatory affairs + Oncology product development experience… more
    Sumitomo Pharma (10/11/25)
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  • Director , RA Global

    AbbVie (Florham Park, NJ)
    …Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Director , Regulatory Affairs Global Regulatory ... products in the obesity/metabolic therapeutic area (TA). This individual leads the Global Regulatory Product Team (GRPT and Labeling Regulatory Strategy Team… more
    AbbVie (09/20/25)
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  • 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 ... Your skills could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting… more
    Sanofi Group (10/23/25)
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  • Associate Director , US Commercial…

    Bristol Myers Squibb (Madison, NJ)
    …work and in their personal lives. Read more: careers.bms.com/working-with-us . **Associate Director Commercial Regulatory Affairs ** **Description** : The ... role of Associate Director of US Commercial Regulatory Affairs requires the ability to apply...Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday,… more
    Bristol Myers Squibb (11/22/25)
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  • Director , US Regulatory

    Sanofi Group (Morristown, NJ)
    **Job Title:** Director , US Regulatory Affairs - Advertising and Promotion (Hybrid) **Location:** Cambridge, MA Morristown, NJ **About the Job** Are you ... critical in helping our teams accelerate progress. As the Director , US Regulatory Affairs -...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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  • Director , Early Precision Medicine…

    Bristol Myers Squibb (Princeton, NJ)
    …careers.bms.com/working-with-us . **Position Summary** The Director of Early Precision Medicine Regulatory Affairs leads global regulatory strategy ... Drive the development and actively support the execution of innovative, compliant global regulatory strategies that enable cutting-edge biomarkers and diagnostic… more
    Bristol Myers Squibb (12/03/25)
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  • Director , Regulatory Affairs

    Taiho Oncology (Princeton, NJ)
    …and coordinate regulatory activities of external consultants in consultation with Global Executive Director or designee. + Prepare project and/or status ... Position Summary: With minimal direction the incumbent manages the global regulatory CMC activities except Asia for...be required to perform other duties, as assigned. Job Details Job Family R&D Job Function Regulatory Affairs more
    Taiho Oncology (12/09/25)
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  • Regulatory Affairs Associate…

    GRAIL (Trenton, NJ)
    …with the FDA and/or global health authorities. + Support the US Regulatory Affairs team in preparing submissions such as PMAs, 510(k)s, post-approval ... and review of Standard Operating Procedures and policy guidelines within the regulatory affairs department. + Perform other duties as assigned. **Required… more
    GRAIL (12/03/25)
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