• Regulatory Writing Sr Mgr

    Amgen (Washington, DC)
    …million patients worldwide. It's time for a career you can be proud of. ** Regulatory Writing Senior Manager** **Live** **What you will do** Let's do this. Let's ... include: + Author or oversee the authoring of all regulatory submission documents including Clinical Study Reports, Investigator Brochures, Responses… more
    Amgen (12/13/25)
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  • Regulatory Accountant

    OGE Energy Corp. (Oklahoma City, OK)
    Regulatory Accountant Requisition ID: 1808 Job Category: Managerial / Professional Location: Oklahoma City, OK, US, 73101-0321 Job Description: **JOB INFORMATION** * ... 125872 * Job Grade: Exempt 57 (or) Exempt 56 Associate > Staff > **Senior > Lead** **JOB SUMMARY**...+ Prepare pro forma adjustments and supporting documentation for regulatory rate case filings. + Develop and analyze accounting… more
    OGE Energy Corp. (09/16/25)
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  • Senior Attorney, Product Regulatory

    Bath & Body Works (Columbus, OH)
    …and our planet to help the world live more fully. The Senior Attorney, Regulatory , will provide counsel to the Company's business teams on regulatory matters ... compliance with applicable Consumer Product Safety Commission, Food and Drug Administration, Federal Trade Commission, and Environmental Protection Agency… more
    Bath & Body Works (10/02/25)
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  • Mgr Regulatory Compliance 3

    Huntington Ingalls Industries (Newport News, VA)
    MGR REGULATORY COMPLIANCE 3 Location: Newport News, Virginia, United States Date: Dec 12, 2025 Req ID: 44377 Team: O55 SCM CMPL/OPS/CMCL PRC Entity: Newport News ... of suppliers, staying current with industry practices for various regulatory topics. The ideal candidate will have experience in...graduate + Navy Nuclear Power School (NNPS) graduate + Associate 's Degree or other formal 2 year program and… more
    Huntington Ingalls Industries (12/13/25)
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  • GRA Device Associate

    Sanofi Group (Cambridge, MA)
    …and IVD products, intended to be used alone or in combination with a drug product, leading regulatory efforts in the development and post-marketing stages. The ... of medicine? The race is on to speed up drug discovery and development to find answers for patients...Regulatory Health Authorities, and others. As GRA Device Associate in the GRA Device Digital and Diagnostic team… more
    Sanofi Group (09/20/25)
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  • Associate Vice President - Women's Health…

    Lilly (Boston, MA)
    …preparation of regulatory reports, including INDs, FDA annual reports, regulatory responses and Periodic Adverse Drug Experience Reports (PADERS), ... better for people around the world. **Position Summary:** The Associate Vice President (AVP), Women's Health & Early Clinical...ability to progress new medicines as part of a drug development team. Responsibilities of the role include directing… more
    Lilly (11/27/25)
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  • Associate Director Quantitative Data…

    Sanofi Group (Morristown, NJ)
    … interactions, quantifying benefit-risk relationships, and contributing to regulatory submissions and interactions from first-in-human studies through life-cycle ... **Job Title:** Associate Director Quantitative Data Modeling **Location:** Morristown, NJ...planning. + Good knowledge of industry best practices, global regulatory , processes, standards of drug development. **Demonstrate… more
    Sanofi Group (11/08/25)
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  • Sr. Quality Associate II / Principal…

    Grifols Shared Services North America, Inc (Clayton, NC)
    …(written and verbal) with demonstrated use of domestic (ie Food and Drug Administration CFR) and applicable foreign regulatory agency requirements/guidelines + ... packaging, and warehousing of plasma related products. The Principle Quality Compliance Associate will support hosting external audits and will support and lead… more
    Grifols Shared Services North America, Inc (12/11/25)
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  • Associate Director, Biostatistics

    Otsuka America Pharmaceutical Inc. (Salem, OR)
    …values and will be responsible for providing statistical expertise/input in the drug development including clinical development plan and regulatory submission ... regarding study design and complex analysis issues, FDA issues, and general drug development. + Reviews clinical, statistical, and regulatory literature for… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Associate Director, Biopharmaceutics

    Organon & Co. (Jersey City, NJ)
    …authoring and review of Investigator Brochures, INDs, briefing books and other regulatory documents, as applicable. The Associate Director, Biopharmaceutics will ... **Job Description** **The Position** The Associate Director, Biopharmaceutics will provide expert biopharmaceutical guidance on the pharmacokinetic performance of … more
    Organon & Co. (10/24/25)
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