• Research Specialist - Regulatory/Compliance

    UPMC (Pittsburgh, PA)
    …trials regulations, (ie, Office of Research and Human Protections (OHRP) and Food and Drug Administration ( FDA ) is essential OR 1+ years' experience in ... EAPs, etc), ensuring compliance with 21 CFR 312 and FDA guidance, while supporting timely activation. + Maintain accurate...team. + Support organizational compliance by ensuring all applicable FDA , OHRP, NIH, and HIPAA requirements are met prior… more
    UPMC (10/08/25)
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  • Group Leader - Pheresis

    CSL Plasma (Normal, IL)
    …and donor disconnect. 2 In compliance with SOPs and Food & Drug Administration ( FDA ) guidelines performs venipuncture to begin pheresis process. ... all Health Safety & Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Promotes safety in all actions. May conduct… more
    CSL Plasma (09/06/25)
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  • Title 32 Health Systems Specialist (MI 127 MDG)

    Air National Guard Units (Selfridge, MI)
    …Health and Safety Administration requirements (OSHA), Food and Drug Administration ( FDA ), and Environmental Safety and Occupational Health ... Specialized Experience for this position: An Undergraduate Degree in Health Administration , Health Care Administration (or equivalent), Health Care Management,… more
    Air National Guard Units (10/02/25)
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  • Senior Quality Engineer I - Validations, Risk…

    Integra LifeSciences (Plainsboro, NJ)
    …thorough understanding of the following regulations and guidelines: US Food and Drug Administration ( FDA ) regulations, ISO 9001, ISO 13485:2003, Medical ... manufacture and distribution of medical products is in compliance with corporate policies, US Food and Drug Administration regulations, ISO 9001, ISO 13485,… more
    Integra LifeSciences (10/08/25)
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  • Clinical Research Data Specialist I - Heart…

    Cedars-Sinai (Los Angeles, CA)
    …compliance with all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board. ESSENTIAL JOB ... with all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board. Maintains research practices… more
    Cedars-Sinai (08/24/25)
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  • Regulatory Affairs Specialist II…

    Abbott (Plymouth, MN)
    …and other regulatory requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, international regulations and other regulatory ... to applicable regulatory standards including those set by the FDA or other worldwide regulatory agencies to various international...to support Abbott customers. + May interface directly with FDA and other regulatory agencies if so directed. +… more
    Abbott (09/27/25)
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  • Senior Regulatory Affairs Specialist…

    Abbott (Plymouth, MN)
    …and other regulatory requirements. + Complies with US Food and Drug Administration ( FDA ) and international regulations, other regulatory requirements, ... and submit medical device submissions to regulatory agencies + Interfaces directly with FDA and other regulatory agencies. + Acts as liaison between the Company and… more
    Abbott (09/27/25)
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  • Medical Device Regulatory Affairs Development…

    Abbott (Santa Clara, CA)
    …and other regulatory requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, international regulations and other regulatory ... to applicable regulatory standards including those set by the FDA or other worldwide regulatory agencies to various international...requests for product release. + May interface directly with FDA and other regulatory agencies if so directed. +… more
    Abbott (09/06/25)
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  • Mechanical Engineer

    BD (Becton, Dickinson and Company) (Mebane, NC)
    …satisfaction initiatives. + General knowledge and understanding of the Food and Drug Administration ( FDA ) 21 CFR 820 and International Organization for ... from a more senior level engineer + ISO compliance, FDA 21 CFR 820 compliance, and cGMP efforts -...and cGMP efforts - Understands and has knowledge of FDA and ISO regulations and cGMP. Requires oversight from… more
    BD (Becton, Dickinson and Company) (08/08/25)
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  • Phlebotomist

    CSL Plasma (Kansas City, MO)
    …monitoring and donor disconnect. 2 In compliance with SOPs and Food & Drug Administration ( FDA ) guidelines, performs venipuncture on donors to begin ... all Health Safety & Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Promotes safety in all actions. 14… more
    CSL Plasma (10/08/25)
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