• Associate Director

    Gilead Sciences, Inc. (Parsippany, NJ)
    …their aspirations. Join Gilead and help create possible, together. **Job Description** As an Associate Director , Global Regulatory Affairs, you will act as ... programs. You will lead Regulatory Submission Teams or other Regulatory Project Teams and represent Global Therapeutic Area Regulatory on… more
    Gilead Sciences, Inc. (10/23/25)
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  • Associate Director Regulatory

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …grow and become your best self. Become a **maker of possible** with us. **The Associate Director of Regulatory Affairs** will provide regulatory support ... is not limited to the development and implementation of regulatory strategies for new product submissions, project ...of regulatory strategies for new product submissions, project management for regulatory affairs submissions, handling… more
    BD (Becton, Dickinson and Company) (11/21/25)
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  • Associate Director

    AbbVie (Florham Park, NJ)
    …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director Regulatory Affairs, Chemistry, Manufacturing and ... Leads initiatives internal to RA CMC. + Represents CMC regulatory affairs on project initiatives with other functional areas to drive efficiencies across… more
    AbbVie (12/09/25)
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  • Associate Director

    Kemin Industries (Des Moines, IA)
    Overview Kemin Health is hiring an Associate Director of Regulatory /Scientific Affairs and Quality! In this role, you will be responsible for leading the ... business units' regulatory affairs (RA) and quality assurance (QA) teams by...Project Verification. + Stay abreast of the changing regulatory , legal, quality and competitive landscape. + Assess and… more
    Kemin Industries (09/12/25)
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  • Associate Director , Construction…

    Boston University (Boston, MA)
    ** ASSOCIATE DIRECTOR , CONSTRUCTION & PROJECT SAFETY, Research Compliance** **Job Description** ** ASSOCIATE DIRECTOR , CONSTRUCTION & PROJECT ... at the time of posting. **Position Type** Full-Time/Regular The Associate Director , Construction and Project ...position will provide sign off on design for all regulatory components, as well as performing routine site visits… more
    Boston University (10/03/25)
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  • Associate Director , Digital…

    BeOne Medicines (Emeryville, CA)
    **General Description:** The Associate Director , Digital Clinical Operations - Project Lead, is responsible for coordinating and managing digital initiatives ... and continuous process refinement to ensure digital capabilities meet business needs and regulatory standards. The Associate Director is expected to: +… more
    BeOne Medicines (11/18/25)
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  • Associate Director , IT…

    Bristol Myers Squibb (Indianapolis, IN)
    …aims to be the global leader in radiopharmaceuticals. **Job Description** The Assoc. Director , IT Regulatory , Clinical and Enterprise Systems is an integral part ... patients in need. In this role, you will report directly to the Exec. Director , IT and be primarily responsible for implementing RayzeBio's vision for growth and… more
    Bristol Myers Squibb (12/03/25)
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  • Statistical Project Leader…

    Sanofi Group (Morristown, NJ)
    **Job Title:** Statistical Project Leader ( Associate Director ) **Location:** Morristown, NJ Cambridge, MA _​_ **About the Job** Join the engine of Sanofi's ... and scientific breakthroughs. Join our **EGDS Biostatistics I&I team as Statistical Project Leader ( Associate Director )** and you'll provide statistical… more
    Sanofi Group (12/06/25)
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  • Associate Director

    Glenmark Pharmaceuticals Inc., USA (Elmwood Park, NJ)
    Associate Director , Regulatory Affairs Department: Regulatory Affairs Location: Elmwood Park, NJ START YOUR APPLICATION ... + Update the internal tracker that records all incoming and outgoing regulatory activities/communications for ANDAs/OTCs which may include submissions to FDA and… more
    Glenmark Pharmaceuticals Inc., USA (11/14/25)
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  • Associate Director . Technical…

    Merck (Boise, ID)
    …source systems to regulatory documentation. Under the guidance of dCMC Regulatory Authoring Leadership, the Associate Principal Scientist, Regulatory ... Operational Excellence, Portfolio, Programme, and Project Support, Program Management, Project Management, Project Planning, Regulatory Documents, Risk… more
    Merck (11/27/25)
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