• Quality Assurance Specialist

    Praxair, Inc - a Linde Company (Fresno, CA)
    …assigned locations in training Managers, supervisors and personnel on Company and FDA GMP procedures + Audit/Assess assigned LG&E manufacturing and warehousing ... personnel to ensure Manufacturing and Warehousing locations meet or exceed FDA and corporate Quality requirements. This employee will ensure Quality incidents… more
    Praxair, Inc - a Linde Company (08/16/25)
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  • Facilities & Engineering Manager

    Fortive Corporation (Irvine, CA)
    …PQ validation** for facility, automation, and process systems. + Ensure compliance with ** FDA , EMA, GMP , OSHA, and safety regulations** . + Support **regulatory ... operations, engineering, automation systems, and process improvements** in a ** GMP -regulated manufacturing environment** . This role ensures **compliance, efficiency,… more
    Fortive Corporation (07/22/25)
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  • Validation Associate III

    Wacker Chemical (San Diego, CA)
    …or engineering (Chemical, Mechanical, or related field) + 5-8 years of experience in a FDA and GMP regulated industry. + ISO 7 & ISO 8 gowning experience ... well 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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  • Sr. Quality Engineer

    Abbott (Temecula, CA)
    …engineering experience and demonstrated use of Quality tools/methodologies. Detailed knowledge of FDA , GMP , and ISO 13485 + Solid communication and interpersonal ... requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating procedures, processes,… more
    Abbott (08/14/25)
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  • General Manager, Manufacturing Operations

    System One (Irvine, CA)
    …years of manufacturing experience with 10+ years in a management role + FDA GMP regulation experience + Requires breadth of organizational, professional field ... device manufacturer, is seeking a hands-on change agent to lead operations at a GMP -regulated site-to step into a Site General Manager role. If you thrive in a… more
    System One (08/20/25)
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  • Supervisor, Operations

    ThermoFisher Scientific (Fremont, CA)
    …quality 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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  • Team Leader, Warehouse Logistics - 1st Shift

    Herbalife (Lake Forest, CA)
    …Shipping and inventory control of raw materials, components and finished goods in a FDA , GMP environment. * Ability to analyze data and develop reports. * ... equivalent PREFERRED QUALIFICATIONS * Two (1) years of experience in an FDA , cGMP regulated manufacturing environment. * Oracle software experience preferred. *… more
    Herbalife (08/30/25)
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  • Senior Supplier Development Quality Engineer

    Abbott (Pleasanton, CA)
    …+ Engineering experience and demonstrated use of Quality tools/methodologies + Detailed knowledge of FDA , GMP , ISO 13485, and ISO 14971 + Solid communication and ... Control Plans. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, company policies, operating procedures, processes,… more
    Abbott (08/13/25)
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  • Sr. Quality Engineer

    Envista Holdings Corporation (Pomona, CA)
    …evaluate the current process and process changes. + Maintains a working knowledge of FDA GMP , ISO 13485 standards and other applicable standards. + Documents ... statistical software (Minitab, JMP, etc.) + Certified Quality Engineer preferred. + FDA Quality System Regulation Part 820 and ISO 13485 experience highly desired… more
    Envista Holdings Corporation (06/13/25)
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