• Staff Java Developer

    Abbott (Sylmar, CA)
    …of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements. + Complies with US Food and Drug Administration ... (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and… more
    Abbott (08/08/25)
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  • Health & Safety Senior Specialist

    Vail Resorts (South Lake Tahoe, CA)
    …and in doing so adjust safety strategy to the business. + Address compliance and regulatory safety as well as risk management trends and regulatory focus areas ... and family AND free ski lessons + MORE employee discounts on lodging, food , gear, and mountain shuttles + 401(k) Retirement Plan + Employee Assistance Program… more
    Vail Resorts (08/02/25)
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  • cGMP Manufacturing Specialized Laboratory…

    University of Southern California (Los Angeles, CA)
    …monitoring and surface sampling). Follows established SOPs and adheres to regulatory guidelines, ensuring compliance with cGMP and safety protocols. Maintains ... Demonstrated passion for solving complex scientific issues. Experience with Food and Drug Administration regulations and clinical trials. Strong communication… more
    University of Southern California (08/02/25)
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  • Bilingual Clinical Research Associate I - Ramin…

    Cedars-Sinai (Los Angeles, CA)
    …for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for ... patient contact for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse… more
    Cedars-Sinai (08/01/25)
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  • Sr Embedded Software Engineer (Sr. Java Engineer)

    Abbott (San Diego, CA)
    …of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements. + Complies with US Food and Drug Administration ... (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and… more
    Abbott (07/30/25)
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  • Clinical Research Coordinator I - Department…

    Cedars-Sinai (Los Angeles, CA)
    …position ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA and local Institutional Review Board. **Primary ... concerns regarding data quality and study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit… more
    Cedars-Sinai (07/24/25)
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  • Clinical Research Coordinator I - Department…

    Cedars-Sinai (Los Angeles, CA)
    …position ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA and local Institutional Review Board. **_*This ... concerns regarding data quality and study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit… more
    Cedars-Sinai (07/23/25)
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  • Principal Systems Engineer

    Abbott (Pleasanton, CA)
    …solve technical challenges, and develop intellectual property. + Complies with US Food and Drug Administration (FDA) regulations, other regulatory requirements, ... from varied disciplines including Clinical Medicine, Engineering, Marketing and Regulatory Affairs required. + Medical device industry experience. + Experience… more
    Abbott (07/18/25)
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  • Clinical Research Associate II - Smidt Heart…

    Cedars-Sinai (Los Angeles, CA)
    …completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact with research ... or contact for long term follow-up research participants only. *Assists with regulatory submissions to the Institutional Review Board (IRB) and works closely with… more
    Cedars-Sinai (07/16/25)
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  • Clinical Research Associate I- Smidt Heart…

    Cedars-Sinai (Los Angeles, CA)
    …for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for ... or patient contact for long term follow-up patients only. *Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of… more
    Cedars-Sinai (07/16/25)
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