• Associate Director, Global Labeling Lead

    Takeda Pharmaceuticals (Boston, MA)
    regulatory nuances and requirements. + Knowledge of scientific principles and regulatory /quality systems relevant to drug development. + Ability to create, ... and assures that Takeda labeling content and processes conform to regulatory requirements. Management of Local Exceptions and LOC Interactions + Manages… more
    Takeda Pharmaceuticals (01/17/26)
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  • Sr. Scientist, R&D

    Teleflex (Wyomissing, PA)
    …complications, and clinical trends (eg, infection, thrombosis, dysfunction) to support product design, methodology development, and regulatory submissions. ... junior team members, and leads projects aligned with strategic objectives and regulatory requirements. Acting as a subject matter expert, this position collaborates… more
    Teleflex (12/24/25)
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  • Clinical Research Coordinator (0.5 FTE) - Diabetes…

    Billings Clinic (Billings, MT)
    …benefits, obtaining and documenting informed consent in accordance with ethical and regulatory standards. * Coordinates information and documentation systems and ... human participants by performing a wide range of clinical, regulatory , and administrative responsibilities. Works collaboratively with participants, staff, and… more
    Billings Clinic (12/23/25)
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  • Lead Compliance Engineer, R&D

    Hologic (Newark, DE)
    …new product launches, post-launch changes, and corrective actions to ensure ongoing regulatory compliance. + Support internal and third-party audits, prepare and ... strategies, policies, and processes to ensure **Hologic's** medical products meet regulatory standards and achieve necessary certifications (eg, ISO, FCC, UL, IEEE).… more
    Hologic (12/16/25)
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  • Sr Director, Environmental, Health, Safety,…

    Valent BioSciences (Libertyville, IL)
    …Japan's leading chemical companies, offering a diverse range of products globally that support a wide variety of industries and help enhance peoples' daily lives. ... Care thus related to environmental stewardship, employee health and safety, regulatory compliance, and product quality across the company's biological and chemical… more
    Valent BioSciences (12/04/25)
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  • VP, R&D Quality

    Gilead Sciences, Inc. (Foster City, CA)
    …and help create possible, together. **Job Description** Reporting to the SVP of Global Regulatory Affairs, Patient Safety and Quality, the VP of R&D Quality will be ... but not limited to, clinical compliance and pharmacovigilance, electronic systems and laboratory compliance, and quality documents and training administration.… more
    Gilead Sciences, Inc. (11/13/25)
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  • Manager, Business Development- Fleet

    TECO Energy (Tampa, FL)
    …gas solutions for vehicles. Works in supporting activities related to any applicable regulatory filings in support of compressed natural gas development with the ... legislation, rates, and tariff requirements. Monitor regulatory changes and initiate regulatory filings, if needed, in support of business developments for… more
    TECO Energy (11/06/25)
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  • Risk Control Self Assessment (RCSA) - Senior…

    American Express (New York, NY)
    …+ Assist in additional identification specific risks throughout business processes and systems (along with business process owners) + Support facilitation to ... met (eg, periodic RSCA reviews and update assessment criteria to align with regulatory updates) + Support control monitoring (supplemental to BU process owners… more
    American Express (01/06/26)
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  • Finance Business Partner IT - Sr Analyst

    PPL Corporation (Louisville, KY)
    …and maintenance expenses to support corporate targets. + Responsible for complex regulatory support which includes rate cases, regulatory assets or ... project/task setup, monthly manual accrual journal entries, expense coding support , etc. + Advanced knowledge of computer systems... support corporate targets. + Responsible for complex regulatory support which includes rate cases, … more
    PPL Corporation (10/24/25)
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  • Senior Principal Electrical Engineer

    Medtronic (Northridge, CA)
    …with FDA regulations (21 CFR Part 820), IEC 60601, and ISO 13485 + Support regulatory submissions including 510(k) and PMA applications + Implement design ... controls and verification/validation protocols per medical device standards + Partner with regulatory and quality teams to support submissions, audits, and… more
    Medtronic (01/09/26)
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