• Global Development Lead, Medical Director,…

    Pfizer (South San Francisco, CA)
    …teams responsible for the development of early development assets (including Product Team). + Oversee the development and management of clinical protocols ... investigator brochures, clinical study reports, statistical analysis plan, and regulatory documents. + Provide leadership to early stage clinical scientists… more
    Pfizer (08/08/25)
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  • Director I, Clinical Development

    AbbVie (Irvine, CA)
    …in aesthetics, we're committed to providing the most comprehensive science-based product offerings available. Job Description The Director I will provide direction ... author, edit and review key section of research protocols, reports and regulatory submissions. Responsibilities: + Based on strong medical and scientific experience,… more
    AbbVie (07/09/25)
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  • Lead Investigator, AML and Financial Crimes…

    Intuit (Mountain View, CA)
    …investigators and lead training programs focused on investigative standards and regulatory compliance. + Familiarity with applicable US laws and regulations ... third-party research tools (eg, Chainalysis, WorldCheck, LexisNexis). + Providing guidance to product and or business partners on risks associated with fintech … more
    Intuit (08/28/25)
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  • Scientist II, Analytical Development (Mass Spec…

    Astellas Pharma (South San Francisco, CA)
    …the GMP release of drug substances and drug products as well as in-depth product characterization activities. In addition, the Scientist II will be a point person ... for supporting early stage development and understanding of product behavior throughout the manufacturing process. This will involve collaboration with colleagues… more
    Astellas Pharma (08/08/25)
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  • Director, Global External Manufacturing, OSD

    Gilead Sciences, Inc. (Foster City, CA)
    …intimate collaboration at the Team Leadership level with the Development, Quality, Regulatory , Analytical, Supply Chain, and Product & Portfolio Strategy ... external contract manufacturing network, while ensuring compliance with cGMP, regulatory requirements, and environmental, health, and safety legislations. This… more
    Gilead Sciences, Inc. (06/15/25)
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  • Sr. Quality Engineer

    Envista Holdings Corporation (Pomona, CA)
    …develop, implement, and maintain quality assurance protocols that comply with regulatory requirements and industry standards. The Sr. Quality Engineer will possess ... a deep understanding of quality management systems, regulatory requirements, and risk management principles. The Sr. Quality Engineer will report directly to the… more
    Envista Holdings Corporation (06/13/25)
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  • Strategic Negotiator, Energy Market Development

    Google (San Francisco, CA)
    …development. **Preferred qualifications:** + Experience in clean energy policy and regulatory matters within Texas, particularly relating to electric utilities, rate ... PUCT. + Ability in achieving desired outcomes in Texas's regulatory and legislative arenas, often as part of large...+ Work cross-functionally with others on Google's Global Infrastructure, Product , Public Policy, and other teams to develop policy… more
    Google (09/06/25)
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  • Associate Vice President, Companion Diagnostics

    Merck (Sacramento, CA)
    …and regulatory requirements for diagnostic assays. + Drive diagnostic product innovation and improvement through both in-house R&D efforts and in collaboration ... stakeholders to ensure alignment with clinical development timelines and regulatory requirements. Most importantly, the role requires overseeing CDx development,… more
    Merck (09/03/25)
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  • Sr. Audit Manager- Wealth Management

    City National Bank (Los Angeles, CA)
    …the operational processes to meet bank policies and procedures and regulatory requirements, identify data analytic opportunities, analyze results of testing ... audit methodology and based on industry/institutional knowledge, emerging risks, and regulatory changes and expectations. Key areas of focus and involvement include:… more
    City National Bank (08/21/25)
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  • Clinical Development Program Lead, Neuropsychiatry…

    Bristol Myers Squibb (San Diego, CA)
    …trials and will supervise and have accountability for the clinical components of regulatory filings + Will contribute to overall strategy for specific disease / ... and Communication + Will work closely with colleagues in BMS Research, Development, Regulatory , Medical, Commercial and other key functional areas on a global basis;… more
    Bristol Myers Squibb (08/20/25)
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