• SOFIE (Totowa, NJ)
    …the future of nuclear medicine! SOFIE is seeking a Product Development Specialist to lead the development, implementation, and validation of manufacturing and ... every process meets the highest standards of quality and regulatory compliance (21 CFR 211 and 212). If you're...want to hear from you. Title | Product Development Specialist Location | Totowa, NJ Department | Radiopharmaceutical Contract… more
    job goal (12/20/25)
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  • SOFIE (Totowa, NJ)
    …development in a rapidly growing industry Job Description | Product Development Specialist Title | Product Development Specialist Location | Remote Department ... $80,000-$90,000/YR(based on experience and education) Overview The Product Development Specialist will lead the development, implementation, and validation of… more
    job goal (12/21/25)
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  • SOFIE (Somerset, KY)
    PRODUCT SUPPORT SPECIALIST , RCM Title | Product Support Specialist Location | Homebased with Travel (Any SOFIE Location) Department | Radiopharmaceutical ... Join a company driving innovation in nuclear medicine! As a Product Support Specialist , you'll take the lead in maintaining and optimizing analytical equipment used… more
    job goal (12/19/25)
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  • Ethos Veterinary Health (Bothell, WA)
    …licensing requirements Mentorship from our Lead LVT, a Veterinary Technician Specialist (VTS), for those pursuing their VTS Veterinary Assistants (VAs): Support ... and record patient histories. Collect specimens and perform routine laboratory procedures and tests in hematology, biochemistry, chemistry, microbiology, urinalysis,… more
    job goal (12/23/25)
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  • Regulatory Specialist

    Covenant Health Inc. (Sevierville, TN)
    Overview Regulatory Specialist , Quality Management Full Time, 80 Hours Per Pay Period, Day Shift LeConte Medical Center Overview: LeConte Medical Center is a ... Combined Time Off (CTO) program . Department Overview: The Lab at LeConte Medical Center is a rewarding place...performance related to The Joint Commission, CMS, and other regulatory /licensing agencies. The Regulatory Specialist more
    Covenant Health Inc. (11/20/25)
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  • Regulatory Specialist

    Covenant Health Inc. (Morristown, TN)
    Overview Regulatory Specialist , Quality Management Full Time, 80 Hours Per Pay Period, Day Shift Some local travel required.Some weekend,holiday or night ... and evaluating performance related to The Joint Commission, CMS, and other regulatory /licensing agencies. The Regulatory Specialist is responsible for… more
    Covenant Health Inc. (10/22/25)
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  • Associate Hazard Communication Regulatory

    The US Pharmacopeial Convention (USP) (Frederick, MD)
    …IL, KS, FL, NC, or MN._** **Brief Job Overview** The Associate Hazard Communication Regulatory Compliance Specialist is an entry level position in USP's Hazard ... collaborative, and results-driven work environments. The **Associate Hazard Communication Regulatory Compliance Specialist ** has the following responsibilities:… more
    The US Pharmacopeial Convention (USP) (11/20/25)
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  • Regulatory Affairs Specialist 3…

    Grifols Shared Services North America, Inc (San Diego, CA)
    …countries and regions. Grifols Diagnostic Solutions in San Diego, CA is seeking a Regulatory Affairs Specialist III. The Regulatory Affairs Specialist ... stakeholders are essential for success in this position. To qualify for the Regulatory Affairs Specialist III role, candidates must have a Bachelor's degree… more
    Grifols Shared Services North America, Inc (12/17/25)
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  • Sr. Regulatory Affairs Specialist

    Medtronic (North Haven, CT)
    …for this opening will close on - 30 Dec 2025 **Position Description:** Sr. Regulatory Affairs Specialist for Covidien, LP (a Medtronic company) located in North ... field and four (4) years of experience as a Regulatory Affairs Specialist or related occupation in...generate real solutions for real people. From the R&D lab , to the factory floor, to the conference room,… more
    Medtronic (10/27/25)
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  • Senior Regulatory Affairs Specialist

    Medtronic (Santa Rosa, CA)
    …be based in Mounds View, MN or Santa Rosa, CA. The **Senior** ** Regulatory Affairs Specialist ** will support our innovative Transcatheter Tricuspid Valve Therapy ... and negotiates their approval with the agencies. The Sr Regulatory Affairs Specialist is responsible for assessment...generate real solutions for real people. From the R&D lab , to the factory floor, to the conference room,… more
    Medtronic (12/12/25)
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