• QEHS Manager

    Keurig Dr Pepper (Sacramento, CA)
    …the facility to ensure that the plant is fully operating in compliance with FSMA, FDA GMP , OSHA, EPA regulations and GFSI guidelines. + Lead the root cause ... defined by FSMA, six sigma Quality performance, and 100% compliance to all FDA , EPA and OSHA regulations. **Location:** This position is located at our Sacramento,… more
    Keurig Dr Pepper (05/30/25)
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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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  • Join Our Talent Pool: Quality Assurance Specialist

    Kelly Services (Orange County, CA)
    …processes across multiple projects. + Ensure strict adherence to **industry regulations** (eg, FDA , GMP , ISO) and **company policies** . + Conduct **regular ... , or **manufacturing** industries. + Strong knowledge of **regulatory guidelines** (eg, FDA , GMP , ISO) and industry best practices. + Exceptional… more
    Kelly Services (07/19/25)
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  • Senior Manager Tooling Engineer

    Abbott (San Diego, CA)
    …and monitor effectiveness of engineering systems and procedures to ensure compliance to FDA , GMP and all other applicable agency regulations + Anticipate and ... requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating procedures, processes,… more
    Abbott (07/18/25)
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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 (05/15/25)
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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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  • Senior Director of Manufacturing

    System One (Irvine, CA)
    …years of manufacturing experience with 7-10 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-with future potential to step into a Site General Manager role. If… more
    System One (07/25/25)
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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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  • Engineer II, Supplier Quality Assurance

    Abbott (Pleasanton, CA)
    …+ AssociatesDegree . + Minimum 1 year experience. **Preferred Experience** + Knowledge of FDA , GMP , ISO 13485, and ISO 14971. + Bachelor's degree Apply Now ... Team Member) + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating procedures, processes, and… more
    Abbott (06/20/25)
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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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