• Construction Project Management Specialist…

    The Boeing Company (El Segundo, CA)
    …and contractor relationships while ensuring strict adherence to safety and regulatory standards. The ideal candidates will demonstrate exceptional organizational and ... + Create layouts and conceptual designs compliant with Boeing and other regulatory standards + Develop options to ensure facilities modifications are accomplished… more
    The Boeing Company (12/05/25)
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  • Environmental Health and Safety Professional

    Stantec (Roseville, CA)
    …and support project teams that assist Stantec's clients to meet safety regulatory requirements and maintain effective management systems. Your Key Responsibilities - ... compliance programs - Supporting performance of environmental, health and safety regulatory compliance and program audits - Interacting with project managers, EHS… more
    Stantec (12/03/25)
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  • Medical/Clinical Laboratory Scientist - Per Diem

    Sonora Quest (Susanville, CA)
    …with department compliance with all pertinent laboratory accrediting agency and regulatory requirements (eg, CLIA '88, JCAHO, CAP, OSHA). May be responsible ... laboratory. _Performs all functions according to established policies, procedures, regulatory and accreditation requirements, as well as applicable professional… more
    Sonora Quest (11/26/25)
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  • Associate Director, Biostatistics

    Pfizer (South San Francisco, CA)
    …analysis, providing data interpretation, and contributing to clinical publication and regulatory submissions. + Provides statistical input to study designs and can ... of results, and collaborate on the reporting of clinical trial results to regulatory authorities and the scientific community by contributing to the clinical study… more
    Pfizer (11/19/25)
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  • Director, Biologics Analytical Development…

    Gilead Sciences, Inc. (Foster City, CA)
    … substance and drug product. + Proven track record in drafting regulatory documentation at all stages, including **IND, BLA, and PAS** filings. + Demonstrated ... deliverables. + Serve as an author and reviewer of CMC sections in regulatory filings, and support interactions with health agencies. + Collaborate across Gilead… more
    Gilead Sciences, Inc. (11/08/25)
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  • Associate Director, PV Sciences

    Taiho Oncology (Pleasanton, CA)
    …of our team, you'll have the opportunity to shape the future of drug safety, contribute to groundbreaking research, and advance patient care worldwide. With ... as Business partners). + Effectively manage to ensure compliance with regulatory submissions and internal timelines. + Participate in audit preparedness activities… more
    Taiho Oncology (11/04/25)
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  • Regional Clinical Study Manager

    BeOne Medicines (San Mateo, CA)
    …and reviews local drug labels for region. Provides input on local regulatory approval and reimbursement status of comparator drugs used in study for countries in ... collaboration with other key stake holders to ensure timely submission to regulatory authorities and ECs/IRBs + Accountable for submissions of study in countries… more
    BeOne Medicines (10/29/25)
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  • Physical Therapist

    Banner Health (Susanville, CA)
    …accordance with physician referral, state and national organizational standards, regulatory agencies, and established departmental policies and procedures. This ... team. 3. Documents according to professional practice guidelines set by regulatory agencies. Documents legibly. Completes documentation within the established time… more
    Banner Health (10/04/25)
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  • Sr Device Engineer I

    Gilead Sciences, Inc. (Foster City, CA)
    …Development Engineer to lead technical development efforts for parenteral drug -device combination products, including autoinjectors, prefilled syringes, and needle ... management. + **Author and review technical reports** and contribute to regulatory submissions (IND, NDA, etc.). + **Collaborate cross-functionally** with … more
    Gilead Sciences, Inc. (12/16/25)
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  • Medical Director, Radiopharmaceutical Imaging…

    Bristol Myers Squibb (San Diego, CA)
    …and neuroendocrine tumors. Responsibilities may include support for IND preparation, regulatory authority interactions, design, and execution of Phase 0 to Phase ... brochures, clinical study reports, and review of other clinical trial and regulatory documents + Conduct investigator meetings and lead site qualification and… more
    Bristol Myers Squibb (12/15/25)
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