• AI Solutions Manager, Life Sciences R&D…

    Deloitte (Los Angeles, CA)
    …serve + Limited immigration sponsorship may be available Preferred: + Understanding of pharmaceutical regulatory data and regulatory filing requirements and ... analytics solutions + 4+ years of experience with Life Sciences Pharmaceutical R&D regulatory data lifecycle . Experience to include introducing new technologies… more
    Deloitte (01/15/26)
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  • Business Development Executive - Regulatory

    Cardinal Health (Sacramento, CA)
    …Standards + Drug, Biologic (IV, Injectable) and Medical Device Development + Regulatory Outsourcing + Pharmaceutical Compliance + Product Lifecycle Management + ... **Position Summary** For nearly five decades, Cardinal Health Regulatory Sciences' industry-trained regulatory consultants have provided expertise and guidance… more
    Cardinal Health (11/25/25)
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  • Director, Regulatory Affairs…

    Stryker (Sacramento, CA)
    …disposition and release in addition to Quality Assurance responsibilities.Viewed as pharmaceutical regulatory expert within business. + Leads communication with ... aspects in external agency audits/inspections. + Stays abreast of external pharmaceutical regulatory requirements and expectations. **Education & Special… more
    Stryker (01/13/26)
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  • Director, Oncology Business Development and Global…

    AbbVie (South San Francisco, CA)
    …years regulatory experience. Some portion may include experience related to pharmaceutical regulatory work (eg, other R&D role or specialized training). ... global regulatory strategies. + Preferred Experience: 10+ years' experience in pharmaceutical regulatory activities, with experience as lead regulatory more
    AbbVie (01/13/26)
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  • Principal Regulatory Affairs Specialist…

    Abbott (Alameda, CA)
    …life Sciences, Biology (or equivalent vocational qualifications) . Experienced in regulatory submissions for Pharmaceutical , in vitro diagnostic devices and/or ... the spectrum of customer needs. Projects will focus on driving the regulatory strategy for business partnership initiatives involving Cloud/ Sensor based external… more
    Abbott (01/19/26)
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  • Principal Regulatory Affairs Specialist…

    Abbott (Alameda, CA)
    …Life Sciences, Biology (or equivalent vocational qualifications) + Experienced in regulatory submissions for Pharmaceutical , in vitro diagnostic devices and/or ... working mothers, female executives, and scientists. **The Opportunity** This **Principal Regulatory Affairs Specialist - APAC** position will work on-site at our… more
    Abbott (01/01/26)
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  • Sr. Manager, Regulatory Affairs Cell…

    ThermoFisher Scientific (Carlsbad, CA)
    …and communicate the impact of relevant global regulations, guidelines, and evolving regulatory trends relating to pharmaceutical product development in the area ... helping find cures for cancer. **Discover Impactful Work** As a Sr. Manager, Regulatory Affairs, you will play a crucial role in interpreting and disseminating… more
    ThermoFisher Scientific (01/14/26)
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  • Associate Director, Regulatory Intelligence

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    … intelligence and collaborates with SMEs to interpret the impact of regulatory changes to the pharmaceutical environment. **Job Description** + Oversee ... The Associate Director of Regulatory Intelligence leads the collection and dissemination of...new and updated regulations and guidance that may impact pharmaceutical practices, procedures and controlled documents. + Lead weekly… more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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  • Regulatory Affairs Associate Director, IVD

    GRAIL (Menlo Park, CA)
    …clinical affairs, quality, or program management within the IVD, medical device, or pharmaceutical industries is required. + Regulatory affairs and IVD device ... Regulatory Affairs Certification (RAC) preferred. + Experience in pharmaceutical clinical, statistical, or regulatory settings-especially in oncology,… more
    GRAIL (12/03/25)
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  • Associate Director, Regulatory CMC (Small…

    BeOne Medicines (Emeryville, CA)
    …Veeva is a plus. **Qualifications:** + 8+ years of related pharmaceutical or biopharmaceutical industry regulatory CMC experience. + ... **_General Description:_** BeOne is seeking an experienced and energetic regulatory professional to manage, evaluate, and complete regulatory projects consistent… more
    BeOne Medicines (12/23/25)
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