• Associate Director, Digital Quality

    BeOne Medicines (San Mateo, CA)
    …or related field required. Advanced degree preferred + Minimum of 8+ years in Quality Assurance in a Pharmaceutical / Medical Device industry in a global ... **General Description:** The Associate Director, Digital Quality Management Systems (QMS) Operations and User Experience, is responsible for ensuring the efficient… more
    BeOne Medicines (06/14/25)
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  • Quality System Document Control…

    US Tech Solutions (West Hills, CA)
    …the pharmaceutical or related regulated industry. + Familiar with Quality Systems (change control, deviations, documentation management, and training system). + ... Ability to understand and implement priorities and workload and to establish strong collaborative relationships with peers. + Good communication, diplomacy skills and be able to work effectively with internal stakeholders. + Must be detailed oriented to detect… more
    US Tech Solutions (08/26/25)
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  • Sr Counsel II

    Gilead Sciences, Inc. (Santa Monica, CA)
    …experience. + Must have knowledge of laws and regulations governing pharmaceutical industry, manufacturing, supply chain, quality , regulatory, intellectual ... from interactions and agreements with external parties related to manufacturing, quality , development, and supply chain. + Facilitate the evaluation, selection,… more
    Gilead Sciences, Inc. (06/20/25)
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  • Senior Manager, Global Regulatory Affairs

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …in regulatory affairs or related areas (eg, clinical development, project management, quality assurance, etc.) in pharmaceutical or healthcare related industry. ... and guidelines. - Confirms submission documents are accurate, compliant, and high- quality to allow for smooth and expeditious approvals from regulatory authorities.… more
    Otsuka America Pharmaceutical Inc. (08/22/25)
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  • Senior Global Patient Safety Quality

    United Therapeutics (Sacramento, CA)
    …regulation, Quality Management principles + 5+ years of experience in managing Quality Management Systems/Records in PV in the pharmaceutical industry + 5+ ... we are** We are the first publicly-traded biotech or pharmaceutical company to take the form of a public...about pharmacovigilance! You are a team player who loves quality , compliance, finding solutions and ensuring training standards are… more
    United Therapeutics (08/10/25)
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  • Executive Director of R&D Global Quality

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …Summary** We are seeking an experienced and dynamic Executive Director of R&D Global Quality to join our team. This pivotal role will be responsible for leading a ... global team focused on R&D Quality . This global role includes direct reports in the...and 15+ years of experience in a FDA regulated pharmaceutical and/or medical device industry environment + Strong knowledge… more
    Otsuka America Pharmaceutical Inc. (08/14/25)
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  • Quality Supervisor

    Element Materials Technology (Santa Fe Springs, CA)
    **Overview** Element has a current opening for a ** Quality Supervisor** to join our growing team in Santa Fe Springs, CA. The ** Quality Supervisor** is ... for overseeing the day-to-day QA operations within a GMP-regulated pharmaceutical environment, ensuring full compliance with applicable regulations, client… more
    Element Materials Technology (08/23/25)
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  • Quality Systems Senior Specialist

    AbbVie (Irvine, CA)
    …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Quality Systems Senior Specialist is responsible for providing quality ... support for some or all of the following manufacturing processes: pharmaceutical products, medical devices, combination products and biologics. Specific areas of… more
    AbbVie (08/15/25)
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  • R&D Senior Quality Specialist (Validation)

    AbbVie (Irvine, CA)
    …of validation activities, and preparation of validation documentation within Pharmaceutical Development, with established guidelines for pharmaceutical products ... GMP environment. + Utilize knowledge of GMP concepts relating to Pharmaceutical manufacturing environment to plan, develop, organize, and execute validation… more
    AbbVie (06/21/25)
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  • Sr. Quality Engineer

    Teledyne (Mountain View, CA)
    …air and water quality environmental monitoring, electronics design and development, oceanographic research, energy, medical imaging and pharmaceutical research. ... include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research,… more
    Teledyne (07/12/25)
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