• Nurse Practitioner/Physician Assistant…

    Stanford Health Care (Palo Alto, CA)
    …Furnishing or Prescribing of Drugs; Formulary Protocol] Medications that are not FDA -approved or are used for a non- FDA -approved indication (off-label use) ... collaboration between providers and coordination of community resources. + Ensures compliance with legal, regulatory and clinical policies and procedures. +… more
    Stanford Health Care (08/17/25)
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  • FSQA Quality Control Clerk

    US Foods (Hawthorne, CA)
    …conditions of returned product for proper disposition Performing all duties in compliance with USDA, DDA, OSHA, state and/or local regulations. Company policies and ... levels of responsibility throughout the company in a professional manner . External: USDA/ FDA officials **WORK ENVIRONMENT** . Must be able to work continually in a… more
    US Foods (08/16/25)
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  • Technical Services Manager

    Fortrex (CA)
    …implement and maintain Food Safety and Safety programs within multiple USDA and FDA facilities across a geographic area while effectively promoting the mission and ... assessments to verify adherence to policies and procedures. + Verify compliance to all internal, customer, third-party auditing, and regulatory requirements… more
    Fortrex (08/08/25)
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  • Advanced Practice Provider (NP/PA), Cardiac…

    Stanford Health Care (Palo Alto, CA)
    …Furnishing or Prescribing of Drugs; Formulary Protocol] Medications that are not FDA -approved or are used for a non- FDA -approved indication (off-label use) ... collaboration between providers and coordination of community resources. + Ensures compliance with legal, regulatory and clinical policies and procedures. +… more
    Stanford Health Care (08/08/25)
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  • Quality Operations Specialist I

    Astrix Technology (Irvine, CA)
    …teams (Quality, Manufacturing, R&D, Supply Chain, Finance, etc.). + Ensure compliance with the company's Quality System policies and procedures and applicable ... external requirements and standards, including FDA , ISO 13485, and other worldwide regulatory agencies pertaining...device complaint files and quality records + Knowledgeable of FDA regulations, 21 CFR part 820 and Part 803… more
    Astrix Technology (08/08/25)
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  • Food Safety and Quality Assurance Technician

    Sysco (Fremont, CA)
    …Assurance (FSQA) support/evaluation programs and inspection/audit procedures to ensure compliance of products and processes to corporate and regulatory requirements ... **Education** + Formal job training in TQM principles, SPC, HACCP concepts, CFIA/ FDA regulations would be beneficial. + Formal quality and sensory analysis training… more
    Sysco (08/08/25)
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  • Formulation Scientist II

    ThermoFisher Scientific (Fremont, CA)
    …groups as needed. + Implement and coordinate comprehensive quality assurance measures in compliance with ISO 13485 and FDA regulations. + Drive continuous ... in a cGMP laboratory setting. + In-depth knowledge of ISO 13485 and FDA manufacturing and quality assurance standards. + Strong background in continuous improvement… more
    ThermoFisher Scientific (08/02/25)
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  • Field Customer Support Specialist I

    Charles River Laboratories (Hollister, CA)
    …customer training, and product validations. * Responsible for completing all service and compliance documentation as required by company policy, cGMP and FDA . * ... proudly supported the development of ~85% of the drugs approved by the FDA in 2019. Equal Employment Opportunity Charles River Laboratories is an Equal Opportunity… more
    Charles River Laboratories (07/29/25)
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  • Mechanical Engineer

    Fortive Corporation (Irvine, CA)
    …facility systems, and capital projects with a focus on quality, compliance , and operational excellence. **Key Responsibilities:** Design and develop mechanical ... productivity. Ensure all designs and projects are compliant with GMP, FDA , ISO 13485, and applicable regulatory requirements. **Required Qualifications:** Bachelor's… more
    Fortive Corporation (07/25/25)
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  • Therapeutic Strategy VP, Rare Disease…

    IQVIA (San Francisco, CA)
    …make a significant impact in the field. A strong background in current FDA regulatory expectations and the global landscape in Rare Disease or Pediatrics. Experience ... strategic and therapeutic area guidance for clinical development plans in compliance with applicable regulatory, medical, and ethics guidelines. + Ensure… more
    IQVIA (07/23/25)
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