• Senior Engineer, Quality Manufacturing

    Cordis (Irvine, CA)
    …inspections, and testing, ensuring compliance with Good Manufacturing Practices ( GMP ). + Training: Provide training to manufacturing personnel on quality-related ... practices. + Audit Support: Support internal and external audits, including FDA inspections, by providing documentation, data, and expertise related to manufacturing… more
    Cordis (08/22/25)
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  • Maintenance Supervisor

    Keurig Dr Pepper (Victorville, CA)
    …production standards and in accordance with Food and Drug Administration ( FDA ), United States Department of Agriculture (USDA), Good Manufacturing Practices ( ... GMP 's), Hazard Analysis and Critical Control Points (HACCP), and all other governmental policies, procedures, and regulations. + Ensure accuracy of all aspects of the… more
    Keurig Dr Pepper (08/21/25)
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  • Reagent Fill Tech II - TFZ Manufacturing

    Grifols Shared Services North America, Inc (San Diego, CA)
    …archives Manufacturing log sheet records. + Demonstrate processes during audits, including ISO, FDA and internal audits. + Follows all safety rules. + Must be able ... knowledge of laboratory safety and record keeping. Working knowledge of GDP, GMP and ISO Reg. Blood Borne Pathogen Training. Intermediate knowledge of Microsoft… more
    Grifols Shared Services North America, Inc (08/21/25)
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  • Sr Manager, Manufacturing

    ThermoFisher Scientific (San Francisco, CA)
    …(Mon-Fri) **Environmental Conditions** Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail ... commercial drug substance manufacturing, or commercial drug product manufacturing in an FDA regulated environment is required. + 5 years consistent track record of… more
    ThermoFisher Scientific (08/20/25)
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  • Senior NPD Manufacturing Engineer

    Stryker (San Jose, CA)
    …engineering test procedures to manufacturing test procedures + Ensure adherence to GMP and safety procedures. **What You Need:** + Bachelor's Degree, required + ... of applicable domestic and international regulations and quality system standards - FDA QSR, MDD, ISO13485, ISO9001, etc. + Experience in independently executing… more
    Stryker (08/19/25)
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  • Material Handler

    Aerotek (San Diego, CA)
    …+ Proficiency in data entry with ERP systems. + Experience in an FDA regulated environment. + Ability to use pallet jacks, forklifts, and automated shipping ... + Demonstrated word processing and data entry skills. + Familiarity with GMP environment. **Additional Skills & Qualifications** + Ability to obtain and maintain… more
    Aerotek (08/19/25)
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  • Quality Systems Senior Specialist

    AbbVie (Irvine, CA)
    …system. May be required to prepare and present data during regulatory audits ( FDA , EMA, Anvisa, etc) and internal audits. *Interact with internal and external ... biological or device related products. + Knowledge of QA systems and GMP compliance requirements including regulations and standards affecting device, biologics, and… more
    AbbVie (08/15/25)
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  • QA Inspector 2nd Shift - Personal Care

    Astrix Technology (San Bernardino, CA)
    …observations. + Ensure all products align with industry regulations such as FDA guidelines and contribute to continuous improvement efforts. + Collaborate with ... diploma or equivalent. + Experience as a QC/QA Inspector in a GMP -regulated environment, ideally in personal care or pharmaceutical manufacturing. + Sharp attention… more
    Astrix Technology (08/15/25)
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  • Animal Care Technician I

    Charles River Laboratories (Redwood City, CA)
    …by delivering operational and cost efficiencies through the strategic insourcing of GMP , GLP and non-GLP research services from discovery through safety assessment. ... 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… more
    Charles River Laboratories (08/14/25)
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  • Technical Training Specialist, QO Environmental…

    Grifols Shared Services North America, Inc (Los Angeles, CA)
    …knowledge of manufacturing processes, laboratory practices, and strong knowledge of GMP and other related compendia is essential. + Requires outstanding verbal ... experience is also required. + Minimum 4+ years of relevant experience in a FDA regulated industry including a minimum of 2 years of experience in training,… more
    Grifols Shared Services North America, Inc (08/14/25)
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