• Senior Clinical Research Scientist

    Danaher Corporation (Sunnyvale, CA)
    …development, registration and commercialization of products. This position is part of Clinical Affairs and will be an Onsite Role in Sunnyvale, CA. The senior ... opportunity to collaborate with other Cepheid scientists, external partners, Government Affairs , Medical and Scientific Affairs on developing the product… more
    Danaher Corporation (06/11/25)
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  • Sr. Manager, Digital Health Technologies Search…

    AbbVie (South San Francisco, CA)
    …Team is an innovative group that combines medical knowledge, digital technologies, regulatory , and data science expertise to develop and validate digital health ... DHT is identified and evaluated with rigor to meet the scientific, regulatory , operational, quality, and strategic requirements. + Lead multiple categories of DHT… more
    AbbVie (08/27/25)
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  • Director, Research and Development

    Unilever (Carson, CA)
    …to ensure quality, safety, and regulatory compliance. + Collaborate closely with Regulatory Affairs to ensure regulatory requirements are met during ... advanced skincare products. The ideal candidate will partner across departments- regulatory , operations, marketing, and corporate R&D-to drive product pipeline… more
    Unilever (08/19/25)
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  • Associate Director, Global Regulator Strategy,…

    Bristol Myers Squibb (San Diego, CA)
    …(Masters, PhD , PharmD, BSN, etc.) with at least 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements** + ... personal lives. Read more: careers.bms.com/working-with-us . **Associate Director, Global Regulatory Strategy, Neuroscience** **Position Summary:** The selected candidate will… more
    Bristol Myers Squibb (08/28/25)
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  • Director, GxP Auditing

    Gilead Sciences, Inc. (Oceanside, CA)
    …and complex supply chains. + Certification in auditing (eg, ASQ, IRCA) or regulatory affairs . + Familiarity with digital audit tools and data analytics ... and regulatory awareness across the organization. **Basic Qualifications:** + PhD with 8+ years of relevant experience in the pharmaceutical industry OR… more
    Gilead Sciences, Inc. (08/14/25)
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  • Sr Manager, IT Business Analysis - SAP BRH…

    Gilead Sciences, Inc. (Foster City, CA)
    …+ Collaborate with cross-functional teams, including manufacturing, quality control, and regulatory affairs , to design SAP BRH solutions that optimize ... deep expertise in SAP BRH & SAP QM module, regulatory compliance (such as GxP and FDA), and life...+ Master's Degree and 6 Years' Experience OR + PhD + 8+ years of experience with SAP, specifically… more
    Gilead Sciences, Inc. (07/10/25)
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  • Vice President, Global Program Lead Neuroscience

    Bristol Myers Squibb (San Diego, CA)
    …plan (IDP) in partnership with the cross functional GPT members + Participates in regulatory filings (NDA, BLA filings) as well as develops strategy for orphan drug ... maximize program impact + Actively supports Investor Relations and Public Affairs in managing external BMS communications **Integrates commercialization inputs and… more
    Bristol Myers Squibb (08/29/25)
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  • Chair, Department of Radiology

    Stanford University (Stanford, CA)
    …technology at its eight distinct imaging centers and affiliated Veteran's Affairs site: Stanford Hospital and Outpatient Clinics, Stanford Children's Hospital and ... the decades-long investment the department has made into meeting regulatory qualifications, implementing training, and adhering to high-performance standards for… more
    Stanford University (08/07/25)
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  • Senior Clinical Research Specialist MDR

    J&J Family of Companies (Irvine, CA)
    …+ Cooperates with cross-functional teams (Research & Development, Complaint Handling, Quality/ Regulatory , Medical Affairs , Medical Safety) to ensure safety and ... with the necessary stakeholders (clinical study team, medical, clinical sites, regulatory , data management) on safety activities related to clinical studies and… more
    J&J Family of Companies (08/29/25)
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  • Associate Director, Statistics - (Hybrid)

    AbbVie (Irvine, CA)
    …of work may include clinical trials, patient safety, and global medical affairs . The Associate Director works in partnership with experts in multiple disciplines ... advance medicines to our patients. Responsibilities: + Provide expertise/lead regulatory submission and product life-cycle management strategy planning and… more
    AbbVie (08/30/25)
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