• 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 ... guidances, and communicates changes in regulatory CMC information to project teams and senior ... guidance. + Collaborates with colleagues across the global CMC RA organization, Gilead Regulatory Affairs more
    Gilead Sciences, Inc. (06/27/25)
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  • Regulatory Affairs Assoc II…

    Gilead Sciences, Inc. (Foster City, CA)
    …of Regulatory Affairs Associate II, CMC sits in Gilead's CMC Regulatory Affairs - Small Molecule Group. Responsibilities and qualifications are ... regulatory strategies. + Under the guidance of more senior staff, oversees the preparation of CMC ...more senior staff, oversees the preparation of CMC regulatory submissions for investigational and commercial… more
    Gilead Sciences, Inc. (07/29/25)
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  • Senior Director, Global Regulatory

    BeOne Medicines (San Mateo, CA)
    …including BeOne's Senior Management. This role blends deep expertise in regulatory affairs with best-in-class project management skills to ensure timely, ... **General Description:** The Senior Director of Global Regulatory Project...both internally and with external partners. + Collaborate with Regulatory Affairs , Clinical, CMC , Quality,… more
    BeOne Medicines (08/08/25)
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  • Senior Director, Regulatory

    Ascendis Pharma (Palo Alto, CA)
    …United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology. The Sr . Director, Regulatory Affairs will serve as the therapeutic ... trials as well as Life Cycle Management Strategies. The Sr . Director will work closely with the executive team...devastating diseases. This position will report to the VP, Regulatory Affairs and ideally be based in… more
    Ascendis Pharma (07/25/25)
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  • Senior Manager, Global Regulatory

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …with 5+ years' experience or Master's degree with 2 years' experience in regulatory affairs or related areas (eg, clinical development, project management, ... needed. - Works collaboratively with members of the global regulatory team (GRL, regional leads, CMC -RA, labeling,...the global regulatory team (GRL, regional leads, CMC -RA, labeling, medical writing, regulatory operations, etc.)… more
    Otsuka America Pharmaceutical Inc. (06/19/25)
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  • Associate Director, Search & Evaluation

    AbbVie (San Francisco, CA)
    …of Drug Development (eg, pre-clinical research, clinical development, Regulatory Affairs , Chemistry Manufacturing and Controls ( CMC )). + Experience with ... assessments of individual partnering opportunities to therapeutic area leadership and senior governance committees as well as contributing to Specialty and Discovery… more
    AbbVie (05/28/25)
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  • Senior Scientific Director, Clinical…

    AbbVie (Irvine, CA)
    …required by program needs, in partnership with Discovery, Translational, and CMC colleagues contribute to design and implement translational strategies. May ... opinion leader interactions related to the disease area(s); partners with Medical Affairs , Commercial and other functions in these activities as required, consistent… more
    AbbVie (08/08/25)
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  • Director, Submission Operations Management

    BeOne Medicines (Emeryville, CA)
    …**job:** Accountable and responsible for building and maintaining relationships within Regulatory Affairs and functional organizations including partnering with ... as CMC , Reg Strategy, Clinical/Non-Clinical, Quality/Manufacturing, GTS, Pharmacovigilance and Regulatory Compliance. This position will also play a key role in… more
    BeOne Medicines (08/01/25)
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