• Staff Program Manager (Transplant Diagnostics)

    ThermoFisher Scientific (Allentown, PA)
    …and customer requirements. + Work closely with R&D, Manufacturing Sciences, Quality, Regulatory , Clinical Affairs and Commercial to define project deliverables. ... + Minimum 4 years of project management experience in the life sciences, medical device and clinical experience preferred. + Experience developing RUO and IVD… more
    ThermoFisher Scientific (09/17/25)
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  • Senior Engineer - Systems Engineering (Remote…

    GE Vernova (Wilmington, NC)
    …testing and qualification. + Experience in US and international nuclear regulatory affairs , licensing, laws, rules, regulations, guidance, etc. applicable ... applicable nuclear guidance, and industry standards. + Remain current on nuclear regulatory issues and system, component, and equipment product knowledge. + Use… more
    GE Vernova (09/16/25)
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  • Sr Business Program Manager

    Exelon (Warminster, PA)
    …gas operations, customer service, transmission and substation, distribution system operations, regulatory and external affairs ). + Advanced proficiency in ... Regional Operations, Distribution Operations, Transmission Operations, Corporate Security, Communications, Regulatory , and Legal. The ability to build relationships across… more
    Exelon (09/16/25)
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  • Document Control Coordinator

    Danaher Corporation (New Brighton, MN)
    …to the Sr Manager, Quality Engineering and is part of the Quality Assurance and Regulatory Affairs team located in New Brighton, Minnesota and will be an on-site ... include: + Familiarity with industry standards, such as ISO, FDA, or other regulatory requirements + Strong attention to detail to ensure accuracy and consistency in… more
    Danaher Corporation (09/16/25)
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  • Clinical Research Coordinator A (Department…

    University of Pennsylvania (Philadelphia, PA)
    …trials. Prepare protocols, informed consent, data collection forms and advertisement for regulatory approval. + Organize and participate in site visits from the ... study sponsor and regulatory authorities. Attend investigator meetings for clinical research trials...Life, and Flexible Spending Accounts : Penn offers comprehensive medical , prescription, behavioral health, dental, vision, and life insurance… more
    University of Pennsylvania (09/16/25)
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  • Environmental Planner

    Actalent (Ontario, CA)
    …+ Experience working with tribal, federal, state, and local agencies, especially in regulatory review and intergovernmental affairs + Willingness to travel to ... the preparation of State and Federal environmental documents and ensure regulatory compliance across Southern California. This role offers strong career growth… more
    Actalent (09/16/25)
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  • Revenue Chrg Intgrty Analyst

    University of Michigan (Ann Arbor, MI)
    …master and fee schedules. Analysts are expected to remain current on regulatory updates in accordance with hospital policies, AMA guidelines, Federal and State ... National Uniform Billing Committee standards. Stay current with CMS and other regulatory and payor mandated charge capture guidelines, including revenue code, CPT,… more
    University of Michigan (09/15/25)
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  • Technical Lead - Electrical Systems Design

    GE Vernova (Wilmington, NC)
    …seismic testing and qualification + Experience in US and international nuclear regulatory affairs , licensing, laws, rules, regulations, guidance, etc. applicable ... applicable nuclear guidance, and industry standards + Remain current on nuclear regulatory issues and system, component, and equipment product knowledge + Use… more
    GE Vernova (09/13/25)
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  • Clinical Research Coordinator B/C

    University of Pennsylvania (Philadelphia, PA)
    …including subject recruitment, data entry, subject visits and follow-up, and regulatory documentation. Work directly with study physicians, other research staff, and ... documentation including source documentation, case report forms, essential study documents, regulatory documents, and subject binders. Enter data in electronic data… more
    University of Pennsylvania (09/12/25)
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  • SR Scientist, Bioanalysis

    Boehringer Ingelheim (Fulton, MO)
    …on project core teams. Contributes technical approaches and scientific support to regulatory affairs in meeting regulatory requirements. The primary ... physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to… more
    Boehringer Ingelheim (09/12/25)
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