• Senior Manager, CMC Global…

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …discipline. + RAC certification will be a plus. **Experience** : + 7+ years in Regulatory Affairs CMC , with significant experience in small molecules is ... **Job Summary** The Chemistry, Manufacturing and Controls ( CMC ) Global Regulatory Affairs (GRA) professional is responsible for developing and executing… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Intern - PDM - CMC Regulatory

    Gilead Sciences, Inc. (Foster City, CA)
    …summer internship is available in the CMC (chemistry, manufacturing and controls) Regulatory Affairs Department at the Foster City, CA, campus of Gilead ... an Undergraduate/Graduate Program with a focus in chemistry, biology, regulatory affairs or closely related subject. The...summer intern will provide support in the preparation of regulatory CMC submissions for investigational and marketed… more
    Gilead Sciences, Inc. (01/05/26)
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  • Senior Regulatory Affairs

    Parexel (Sacramento, CA)
    regulatory requirements and processes to a major, dedicated client partnership. As a Senior Regulatory Affairs Associate, you will serve as the primary ... to Parexel! We are currently seeking a highly motivated Regulatory Affairs professional to join Parexel and...in line with local legislation (renewals, PSURs, label updates, CMC changes). * Execute timely data entry and validation… more
    Parexel (12/20/25)
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  • Associate Director, Regulatory

    Sumitomo Pharma (Sacramento, CA)
    …highly motivated, and experienced individual for the position of **Associate Director, Regulatory Affairs (Oncology).** The Associate Director is part of the ... Global Regulatory Affairs (GRA) team based in the US....the global regulatory lead (GRL) and the CMC regulatory lead in the formulation of … more
    Sumitomo Pharma (10/11/25)
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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. (11/20/25)
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  • Asset Strategy Leader, R&D Aesthetics

    AbbVie (Irvine, CA)
    …brands (Development, Discovery, Development Sciences, Operations, Commercial, Market Access, Regulatory , Safety, Project Management, Medical Affairs , etc., and ... project's primary point of contact for Pipeline Governance and senior management. + Has a broad vision for the...cross-functional teams (eg, Global Commercial Team, Global Brand Team, CMC , Integrated evidence strategy team, Value and Access team,… more
    AbbVie (12/06/25)
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