• Director, Human Factors Engineering

    Abbott (Milpitas, CA)
    …and ensures compliance with company policies and procedures (eg compliance with FDA regulations, etc.) + *Makes and executes operational decisions with a strategic ... degree in Human Factors Engineering, Biomedical Engineering, Electrical Engineering, Computer Science, Mechanical Engineering or other scientific or engineering… more
    Abbott (08/08/25)
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  • Associate Clinical Project Manager

    Abbott (Alameda, CA)
    …clinical project is always "audit ready" (project team training records, central files, system validation , etc.). + If applicable, ensures adequate monitoring is ... regulatory compliance guidelines for clinical trials (eg applicable ISO Standards, FDA ). Strong problem-solving skills. + Strong computer skills. Demonstrated… more
    Abbott (07/22/25)
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  • R&D Software Engineer III

    ManpowerGroup (San Diego, CA)
    …internal standards and regulatory requirements. **Qualifications:** + Bachelor's degree in Computer Science, Engineering, or related field (MS preferred). + 10+ ... years of experience in software/ system development, preferably in connected device or medical device...Experience with medical device regulations (ISO 13485, IEC 62304, FDA 21 CFR Part 820). + Familiarity with cloud… more
    ManpowerGroup (07/16/25)
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  • Food Safety Specialist $70-$80k Quarterly Bonus…

    JBS USA (Manteca, CA)
    …and prerequisite program requirements. This position will ensure compliance to USDA/ FDA guidelines for food safety/SQF and BRC requirements. Also responsible for ... Maintain and lead site specific or customer database management systems (Customer Complaints, PONC Tracking and Reposi Trak) +...other validations + Be capable of doing swabs and validation tests as needed + Have the ability to… more
    JBS USA (07/22/25)
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  • Quality Control Analyst II

    Curia (Camarillo, CA)
    …use of computer software, including Microsoft Office Suite and instrument manufacture-based systems + Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or ... transfers, and validations + Perform QC method development + Perform cleaning validation studies + Assist with the evaluation of new equipment and processes… more
    Curia (06/18/25)
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