• Senior Director , Regulatory

    Bristol Myers Squibb (Indianapolis, IN)
    …radiopharmaceuticals . We are seeking an experienced and motivated **Senior Director , Regulatory Affairs - CMC (Manufacturing)** . This position will ... report to the Head of Regulatory Affairs and will oversee and/or manage CMC regulatory functions within the RayzeBio manufacturing facility located in… more
    Bristol Myers Squibb (08/24/25)
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  • Associate Director , Global…

    Takeda Pharmaceuticals (Boston, MA)
    Affairs CMC team, you will report to the Senior Director Global Regulatory Affairs CMC . **How you will contribute:** + Plan, execute and manage ... therapies to patients worldwide. Join Takeda as an Associate Director , GRA CMC Small Molecules where you...where you will oversee the development and execution of regulatory CMC development and registration strategies. You… more
    Takeda Pharmaceuticals (07/08/25)
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  • Senior Advisor/ Director , Global…

    Lilly (Indianapolis, IN)
    …who need them all over the world. The Senior Advisor/ Director in Global Regulatory Affairs - CMC Pre-approval Small Molecules will leverage CMC ... make life better for people around the world. Lilly is looking for regulatory CMC scientists to join us in developing and bringing life-changing new medicines to… more
    Lilly (07/02/25)
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  • Director , CMC Regulatory

    Gilead Sciences, Inc. (Foster City, CA)
    …and inflammation, and serious respiratory and cardiovascular conditions. **KEY RESPONSIBILITIES** The Director , CMC Regulatory Affairs for Biologics ... of an approved/ harmonized regulatory control strategy. + Partner across CMC Regulatory Affairs , PDM, and other functional groups across Gilead. + Lead… more
    Gilead Sciences, Inc. (08/15/25)
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  • Senior Advisor/ Director Global…

    Lilly (Indianapolis, IN)
    …them all over the world. The Senior Advisor/ Director Post approval scientist in Global Regulatory Affairs - CMC commercial solid oral products will use ... better for people around the world. Lilly is looking for post approval regulatory CMC scientists to join us in delivering life-changing new medicines to patients… more
    Lilly (09/03/25)
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  • Director , Regulatory Affairs

    Gilead Sciences, Inc. (Foster City, CA)
    … Information Management system. **Qualifications** + Bachelor's degree and 12+ years of experience in CMC Regulatory Affairs ( CMC RA) or other relevant ... guidance. + Collaborates with colleagues across the global CMC RA organization, Gilead Regulatory Affairs , and affiliates on internal meetings and… more
    Gilead Sciences, Inc. (06/27/25)
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  • Sr Director , Regulatory

    Gilead Sciences, Inc. (Foster City, CA)
    …a scientific or technical discipline required (advanced degree preferred) - with biopharma and/or regulatory affairs experience of 14+ years with a BA/BS or 12+ ... in digital or innovation roles preferred. + Strong understanding of CMC regulatory submissions and the structure/content of Module 3. + [Preferred]:… more
    Gilead Sciences, Inc. (09/04/25)
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  • Associate Principal Scientist, Regulatory

    Organon & Co. (Plymouth Meeting, PA)
    …Scientist (Associate Director ) is responsible for developing and implementing Regulatory Chemistry, Manufacturing & Controls ( CMC ) strategies for assigned ... business processes and systems. + Demonstrate an understanding of regulatory affairs and apply this understanding to...the product lifecycle + Identify, communicate and escalate potential regulatory issues to Organon Regulatory CMC more
    Organon & Co. (07/22/25)
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  • Exec Director , Regulatory

    Gilead Sciences, Inc. (Washington, DC)
    …degree with directly relevant professional experience in small molecule and biologics development, global CMC regulatory affairs and CMC technical areas ... with an MA/MS, PhD, PharmD, or MD. + Demonstrated track record in leading CMC regulatory affairs initiatives, innovative CMC regulatory strategies,… more
    Gilead Sciences, Inc. (08/08/25)
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  • Post-Doctoral Fellow Regulatory

    Boehringer Ingelheim (Ridgefield, CT)
    …or more therapeutic areas covering multiple dosage forms while interacting effectively within Regulatory Affairs and across CMC stakeholder functions, as a ... Scientific Communications, clinical operations, translational medicine and clinical pharmacology, and regulatory affairs . This position will require the Fellow… more
    Boehringer Ingelheim (08/30/25)
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