• Sr Scientist, Biomarker - Oncology

    Gilead Sciences, Inc. (Foster City, CA)
    …protocols and associated documents as well as participate in meetings with regulatory authorities. In addition, the scientist will direct the implementation of ... review and coordinate biomarker plans in clinical trial protocols, regulatory documents and collaboration agreements. + Must be able...of immunology and/ or oncology or other related medical science field with a minimum of 5 years of… more
    Gilead Sciences, Inc. (08/08/25)
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  • Director, Facilities & Equipment Quality Strategy,…

    Gilead Sciences, Inc. (Santa Monica, CA)
    …advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great leader. People Leaders ... comply with current Good Manufacturing Practices (cGMPs), company policies, and regulatory requirements. + Sponsor and oversee process improvements and harmonization… more
    Gilead Sciences, Inc. (08/08/25)
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  • Project Manager I

    Charles River Laboratories (Northridge, CA)
    …multiple high-impact projects simultaneously. Experience in client communication, regulatory environments, and process improvement is highly desirable. Essential ... workflows. + Collaborate with departments such as R&D, Quality, Regulatory , and Manufacturing to meet project goals. + Ensure...the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us… more
    Charles River Laboratories (08/08/25)
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  • Environmental Compliance Specialist

    Stantec (Solana Beach, CA)
    …to evaluate diverse facility types for conformance to federal, state, and local regulatory standards + Act independently and as part of a multi-media audit team ... control, etc. " " **Your Capabilities and Credentials** + Knowledge of environmental regulatory standards and programs + Knowledge of regulatory program areas,… more
    Stantec (08/07/25)
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  • Senior Specialist, Conformance

    Bayer (Berkeley, CA)
    …metrics for daily DR record management; + Maintain knowledge of current regulatory practices including a current understanding of USP/EP, cGMP regulations, ICH, and ... management, Risk Management, etc.) + Expertise in cGMP and regulatory requirements (FDA, EMA, ICH, etc.) + Knowledge/experience conducting...this unique opportunity, and want to impact our mission Science for a better life, we encourage you to… more
    Bayer (08/07/25)
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  • Environmental Health and Safety Consultant

    Stantec (Roseville, CA)
    …and studies, including environmental remediation and restoration. + EHS regulatory compliance assessments and audits at industrial and manufacturing client ... and/or state environmental regulations. + Technical consulting for clients on regulatory compliance matters including permit management, routine regulatory more
    Stantec (08/07/25)
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  • Clinical Research Coordinator (Hybrid Opportunity)

    Stanford University (Stanford, CA)
    …estimated time, other activities that the RA may support will encompass data science and technology related research and thus training and experience is desirable ... + Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. + Determine eligibility… more
    Stanford University (08/07/25)
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  • Sr Principal Environmental Health and Safety…

    Northrop Grumman (Sunnyvale, CA)
    …+ Conduct internal compliance inspections to identify actions necessary to meet regulatory requirements + Assist in continuous improvement of the culture, and ... improve EHS awareness throughout the site + Interface with regulatory representatives, senior management, site personnel, and sector program managers **Additional… more
    Northrop Grumman (07/26/25)
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  • Laboratory Technical Specialist

    IQVIA (Valencia, CA)
    …and quality control performance data reviews in accordance with policy and regulatory guidelines. + Validate assays through statistical analysis of local laboratory ... and investigations. + Develops and maintains the yearly schedules for regulatory functions and performs data analysis for performing linearity and comparison… more
    IQVIA (07/26/25)
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  • Director Biocompatibility

    Abbott (Santa Clara, CA)
    …all the new and existing products to meet the existing and emerging regulatory requirements, particularly the EU Medical Device Regulations (EU MDR) and ISO 10993 ... on risk assessments (products/materials, impurities, leachables and extractables), author regulatory documents, and interact with Health Authorities. + Responsible… more
    Abbott (07/24/25)
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