• Sanitation Supervisor

    Lactalis American Group Inc. (Tulare, CA)
    …Supervisor Tulare, CA (http://maps.google.com/maps?q=10800+Ave+184+Tulare+CA+USA+93274) * Quality Job Type Full-time Description TITLE: Sanitation Supervisor ... yourEXPERTISEto ours Key responsibilities for this position include: + Assists the Quality Department manager to enhance the technical and financial performance of… more
    Lactalis American Group Inc. (08/15/25)
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  • Supervisor, Operations

    ThermoFisher Scientific (Fremont, CA)
    … and regulatory standards **Knowledge, Skills, Abilities** + Knowledge of manufacturing techniques, FDA , GMP , and ISO 13485 compliance + Proven ability to ... Shift (Days) **Environmental Conditions** Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Laboratory Setting, Office, Some degree of PPE… more
    ThermoFisher Scientific (08/01/25)
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  • Scientist III, Particles manufacturing

    ThermoFisher Scientific (Fremont, CA)
    …regulatory compliance for medical devices or diagnostics. + Strong technical skills in FDA , GMP , ISO 13485 compliance, process improvement, and development. + ... lbs. without assistance, Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Laboratory Setting, Some… more
    ThermoFisher Scientific (07/13/25)
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  • Plant Engineer

    Lactalis American Group Inc. (Tulare, CA)
    …solutions. + Ensure compliance with all applicable regulatory and safety standards (eg, FDA , OSHA, USDA, GMP ). + Develop equipment and process specifications, ... improvement initiatives. The Plant Engineer collaborates closely with maintenance, production, quality , and safety teams to support safe and efficient manufacturing.… more
    Lactalis American Group Inc. (08/21/25)
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  • Production Clerk

    Fujifilm (Santa Ana, CA)
    …experience in bioscience, pharmaceutical or medical devices industry. + Working knowledge of GMP , GDP, ISO, FDA and OSHA regulatory requirements. + Working ... and innovation, and we pride ourselves on delivering unparalleled quality and service to our partners. If you're ready...ERP system. + Working knowledge of batch records including GMP and GDP rules governing their accuracy and completeness.… more
    Fujifilm (08/19/25)
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  • Formulation Scientist II

    ThermoFisher Scientific (Fremont, CA)
    …working in a cGMP laboratory setting. + In-depth knowledge of ISO 13485 and FDA manufacturing and quality assurance standards. + Strong background in continuous ... lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish,… more
    ThermoFisher Scientific (08/02/25)
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  • Chemist II

    Element Materials Technology (Santa Fe Springs, CA)
    …experiments and observations + Assist in audit preparedness and for participating in quality audits with FDA , other Regulatory Agencies, and customers, as needed ... II** is responsible for performing testing in a pharmaceutical Quality Control laboratory. All work will be conducted in...state and federal regulations, including but not limited to GMP , DEA, FDA , etc. **Skills / Qualifications**… more
    Element Materials Technology (08/22/25)
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  • Vice President, Strategic Sourcing

    Vera Therapeutics (Brisbane, CA)
    …solutions, cost sheets, etc. Compliance & Regulatory Oversight * Ensure full compliance with FDA , EMA, GMP , GCP, GDP, and SOX regulations across all supply chain ... will oversee clinical and commercial supply chains, ensuring alignment with FDA /EMA standards, cold chain logistics protocols, and enterprise-wide risk management… more
    Vera Therapeutics (08/09/25)
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  • Associate Director - Critical Utilities

    Takeda Pharmaceuticals (Thousand Oaks, CA)
    …the safe, compliant, and uninterrupted delivery of utilities to our 24/7 commercial GMP biologics manufacturing operations. Success is achieved by leading a team of ... and technicians in the operation, maintenance, repair, and improvement of GMP utility systems, including facility systems (eg, HVAC, electrical), high-purity water… more
    Takeda Pharmaceuticals (07/23/25)
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  • Director, Small Molecule Process Development

    Amgen (Thousand Oaks, CA)
    …R&D and commercialization to the department + Extensive knowledge of GLP and GMP activities + Clearly understands and applies knowledge of regulatory requirements ( ... FDA , ICH, USP, etc.) to completion of projects +...experience with regulatory requirements for API/Product (CMC for IND/NDA, GLP/ GMP , ICH) + Experience in authoring briefing books, investigational… more
    Amgen (07/09/25)
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