• Development Scientific Director, I&I

    Sanofi Group (Morristown, NJ)
    …Study Units, and investigators + Contribute to the clinical part of Common Technical Document for submission to regulatory bodies (FDA, EMA, PMDA etc.) and ... leadership of the Global Project Head, with the Global safety Officer, Regulatory Strategist and other key functional representatives to deliver development strategy… more
    Sanofi Group (11/21/25)
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  • Quality Assurance Coordinator (Entry Senior Level)

    University of Colorado (Aurora, CO)
    …Requisition: #37493** **Job Summary:** **Key Responsibilities:** + Participates in regulatory submissions for Biological License Applications (BLA), filings, and ... communications with regulatory and accreditation agencies including audits including but not...to a patient. + Reviews and assists with the preparation of occurrence (deviation) reports, complaints, and corrective and… more
    University of Colorado (11/09/25)
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  • Paralegal II

    LA Care Health Plan (Los Angeles, CA)
    …technology and other related research platforms. Attention to detail, accuracy in document preparation and review, and strong organizational skills. Must be ... and provider contractual documents, policies and procedures, and agreements), and regulatory matters. The Paralegal II researches and analyzes law, investigates… more
    LA Care Health Plan (10/13/25)
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  • Environmental Specialist 1/Trainee 1/Trainee 2 (NY…

    New York State Civil Service (Hornell, NY)
    …The incumbent in a Regional Office may supervise engineering technicians in the preparation and processing of environmental permit requests and other regulatory ... environmental analysis experience which must include substantial involvement in the preparation and review of environmental impact analyses, requiring knowledge and… more
    New York State Civil Service (12/19/25)
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  • Animal Control Officer IV

    The County of Los Angeles (Los Angeles, CA)
    …laws, including the investigation of violations and court prosecution for an animal control/ regulatory agency. One year of the experience must have been at the level ... of Animal Control Officer III* for an animal control/ regulatory agency- AND - Possession of certification indicating successful...examinations and your test scores may be transferred. Test Preparation Study guides and other test preparation more
    The County of Los Angeles (12/03/25)
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  • Scientist, Process Technology Operations

    Bristol Myers Squibb (Devens, MA)
    …and interpretation of data trending, review and approval of change controls and preparation of regulatory filings. + Performs root cause investigations and ... all assigned projects. + Supports process technology transfer, process validation and the preparation of CMC documentation for regulatory filings for BMS Devens… more
    Bristol Myers Squibb (12/24/25)
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  • Senior Medical Writer- FSP

    Parexel (Jefferson City, MO)
    …and applicable regulatory guidelines and regulations. + Broad experience in preparation of all types of clinical regulatory documentation. Experience in ... develop, and finalize key clinical documents for submission to regulatory authorities, without the need for any supervision or...prepare any type of medical writing deliverable. + Revise document drafts based on the review comments from team… more
    Parexel (12/13/25)
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  • Senior Paralegal

    Red Cat Holdings (Salt Lake City, UT)
    …legal team. This role requires a deep understanding of government contracting, regulatory licensing, document retention, and litigation oversight. The ideal ... Oversee document retention policies to ensure compliance with legal and regulatory requirements. + Manage the legal document repository, ensuring secure and… more
    Red Cat Holdings (10/24/25)
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  • Environmental Specialist I, II, III- Air…

    Williams Companies (Wysox, PA)
    …with preparation of environmental reports, plans and inventories for regulatory authorities + Responds to requests from internal and/or external customers + ... remain within legal limits. Your day includes gathering operational data, submitting regulatory reports, and handling permit renewals under tight deadlines. You will… more
    Williams Companies (11/18/25)
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  • Principal Medical Writer / Senior Medical Writer…

    Parexel (Jefferson City, MO)
    …to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, investigator ... informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety update/aggregate reports, and… more
    Parexel (12/13/25)
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