• Quality Engineer III

    ManpowerGroup (Fremont, CA)
    …quality assurance experience. + In-depth knowledge of quality management systems (ISO, FDA , IVDR, QSR). + Proven experience in product and process validation, risk ... management, and statistical analysis. + Strong problem-solving and analytical skills with a data-driven approach. + Excellent written and verbal communication skills to effectively collaborate with cross-functional teams. **What's in it for me?** + Medical,… more
    ManpowerGroup (08/15/25)
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  • Associate Vice President, Clinical Data Management

    Amgen (Thousand Oaks, CA)
    …a pharmaceutical, biotech, or CRO environment. + Expertise in GCP, ICH, FDA , EMA regulations, data governance, and clinical trial data standards (CDISC, SDTM). ... + Experience within cross-functional collaborations, leadership, and strategic planning skills, ensuring operational excellence and compliance while driving innovation in data management to support Amgen's global clinical development efforts. + Expertise in… more
    Amgen (08/14/25)
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  • Senior Manager, Regulatory Affairs, Advertising…

    BeOne Medicines (San Mateo, CA)
    …necessary. + Maintains up to date information regarding initiatives by FDA , Health Canada, and other applicable regulatory authorities related to ... advertising/promotion. + Integrates functional expertise with business knowledge to solve problems and make good decisions for the overall business. + Adheres to Company's policies and supports management decisions and goals. **Skills and Experience:** +… more
    BeOne Medicines (08/14/25)
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  • Executive Director, Clinical Development - Rare…

    Amgen (Thousand Oaks, CA)
    …toxicology approaches + Knowledge of Good Clinical Practices (GCP), FDA regulations and guidelines, and applicable international regulatory requirements + ... Ability to effectively present ideas and document complex medical/clinical concepts in both written and oral communication + Ability to analyze and interpret complex datasets + Exercises initiative in meeting goals and drives innovation in projects They will… more
    Amgen (08/14/25)
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  • Animal Care Technician I

    Charles River Laboratories (Redwood City, CA)
    …worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that elevate your ... quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.… more
    Charles River Laboratories (08/14/25)
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  • Executive Director of R&D Global Quality (Remote)

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …**Qualifications** + Bachelor's degree and 15+ years of experience in a FDA regulated pharmaceutical and/or medical device industry environment + Strong knowledge of ... current global Good Clinical Practice (GCP) for designing, recording and reporting trials that involve the participation of human subjects. Managing compliance with this standard to provide assurance that the rights, safety and wellbeing of trial subjects are… more
    Otsuka America Pharmaceutical Inc. (08/14/25)
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  • Senior Director, Regulatory Affairs

    Stryker (San Jose, CA)
    …Demonstrated knowledge and application of regulatory requirements, including ISO, FDA , and International requirements + Demonstrated expertise in regulatory systems ... in a regulated environment + Demonstrated ability to manage complex projects + Demonstrated verbal, written, and interpersonal communication skills + Demonstrated ability to work in a team environment, interact effectively with management from other functions… more
    Stryker (08/14/25)
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  • Phlebotomist (Bilingual)

    CSL Plasma (National City, CA)
    …donor disconnect. + In compliance with SOPs and Food & Drug Administration ( FDA ) guidelines, performs venipuncture on donors to begin pheresis process. + Evaluates ... vein performance of the donor to identify possible problems; makes necessary corrections in order to expedite donation time and ensure product quality and donor safety. Ensures donation process is efficient and makes adjustments when necessary to make the… more
    CSL Plasma (08/14/25)
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  • Quality Control Scientist III

    ThermoFisher Scientific (San Francisco, CA)
    …Skills, Abilities** + Demonstrable understanding of applicable regulatory requirements (ISO, ICH, FDA , EMA and USP) as it relates to analytical method transfer, ... phase-appropriate analytical method qualification and validation, safety testing and drug product stability. + Ability to build, use, and interpret scientific tables, charts, and graphs. + Able to read, comprehend, and make appropriate alterations to documents… more
    ThermoFisher Scientific (08/14/25)
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  • QA Technician (AM Shift)

    Moonlight Companies (Reedley, CA)
    …Qualifications and Skills Required: + Bilingual (Spanish/English) + Prior Knowledge/Experience of FDA , GMP, GAP, HACCP, USDA helpful + Ability to work well in ... a team-based environment with limited supervision + Ability to work in a fast paced environment + Proficiency with basic computer skills, including e-mail, Microsoft Office Pay Range ($16.50 min - $17.00 max)/hour Powered by JazzHR more
    Moonlight Companies (08/14/25)
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