• Validation Associate III

    Wacker Chemical (San Diego, CA)
    …(Chemical, Mechanical, or related field) + 5-8 years of experience in a FDA and GMP regulated industry. + ISO 7 & ISO 8 gowning experience is preferred. + ... as Microsoft Office Suite. + Knowledge of regulatory requirements, including FDA, GMP , and ISO standards. + Requires good written, verbal, and interpersonal… more
    Wacker Chemical (08/28/25)
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  • Bakery Associate

    Aerotek (Sacramento, CA)
    …Skills + Experience in food production or manufacturing environments. + Knowledge of GMP and food safety standards. + Ability to operate and maintain machinery used ... growth and development. Work Environment Work in a manufacturing environment that adheres to GMP standards. The facility can be hot and loud, but it offers a… more
    Aerotek (08/28/25)
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  • Director, Strategist QC & Analytics Cell Therapy

    Bayer (Berkeley, CA)
    …data sets, alongside a comprehensive understanding of regulatory frameworks and GMP compliance. The successful candidate will translate product and process knowledge ... in the context of cell therapy; + Extensive experience working in a GMP environment, with a solid understanding of relevant regulations; + Demonstrated expertise in… more
    Bayer (08/27/25)
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  • Medical Device Assembler

    Kelly Services (Irvine, CA)
    …problems. + Complete documentation such as Device History Records per GDP and GMP requirements. + Support the introduction of new products onto the manufacturing ... line. + Maintain compliance with GMP , ISO, SOP, and safety guidelines. + Maintain clean and organized workstation. + Train other Assemblers and perform quality… more
    Kelly Services (08/26/25)
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  • Supervisor, cGMP Facility Cleaning

    Gilead Sciences, Inc. (Oceanside, CA)
    …perform cleaning operations under strict guidelines for Controlled cleanrooms and GMP laboratory environments. + Continually monitor the cleanroom and laboratory ... accurate and complete records. Review documentation and logbooks and ensure GMP compliance. + Performs sterile and non-sterile stocking, staging and shifting… more
    Gilead Sciences, Inc. (08/26/25)
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  • Senior Metrology Technician (Calibration…

    Wacker Chemical (San Diego, CA)
    …matter expert (SME) for metrology. + Ensures compliance with regulatory standards (eg, GMP , ISO 17025). Plays a key role in strategic planning for metrology programs ... Certified Calibration Technician by ASQ) + 8-10+ years of experience in a FDA and GMP regulated industry. + ISO 7 & ISO 8 gowning experience is preferred. + Ability… more
    Wacker Chemical (08/23/25)
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  • QC Technician - 2nd Shift - Food Manufacturing

    Astrix Technology (Pomona, CA)
    …inspections and environmental monitoring as required. + Execute daily GMP (Good Manufacturing Practices) audits throughout production areas and warehouse ... programs and policies including government regulations, FDA, USDA, AIB, HACCP, GMP , and Allergen Programs. + Ability to work full-time/flexible schedule including… more
    Astrix Technology (08/23/25)
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  • Inventory Fulfillment Associate II

    Grifols Shared Services North America, Inc (San Diego, CA)
    …0-2 years in related experience with AA. Must have at least 1-year GMP experience in a regulated environment. **Primary Responsibilities for Role:** + Interacts ... 0-2 years in related experience with AA. Must have at least 1 year GMP experience in a regulated environment. **Equivalency:** Depending on the area of assignment,… more
    Grifols Shared Services North America, Inc (08/23/25)
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  • Quality Control Chemist I

    Catalent Pharma Solutions (San Diego, CA)
    …that include analytical development, pre-formulation testing, formulation development, GMP (Good Manufacturing Practices) manufacturing and stability storage and ... School Diploma/GED with a minimum of three years of applicable laboratory experience ( GMP exposure preferred) + With a Bachelor's degree, no experience is required.… more
    Catalent Pharma Solutions (08/22/25)
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  • Regulatory Compliance - Senior Analyst

    Kelly Services (Irvine, CA)
    …medical device regulations and standards: 21 CFR Part 820 QSR, ISO 13485, Brazil GMP , Canada Medical Devices Regulations SOR 98-282, Japan's MHLW MO 169, EU MDR ... as required. RESPONSIBILITIES: * Assures that Quality System Audits comply with QSR/ GMP and ISO requirements. * Conducts internal audits of the Quality System… more
    Kelly Services (08/22/25)
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