• QC MLT Scientist

    WuXi AppTec (Middletown, DE)
    …Scientist will perform advanced microbiological laboratory activities in support of drug product manufacturing at WuXi STA's Middletown, DE site. This role ... and documentation in accordance with GMP, corporate quality standards, and regulatory requirements. The QC Microbiology Scientist will support both startup and… more
    WuXi AppTec (09/16/25)
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  • QC Analytical Scientist

    WuXi AppTec (Middletown, DE)
    …expert in analytical chemistry testing and laboratory operations in support of drug product manufacturing at WuXi STA's Middletown, DE site. This role includes ... as well as maintaining compliance with GMP, corporate quality standards, and global regulatory requirements. The QC Analytical Scientist will play a critical role in… more
    WuXi AppTec (09/16/25)
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  • Engineer III/Senior | Power Quality…

    Arizona Public Service (Phoenix, AZ)
    …interaction with research institutes (EPRI, etc.), industry peer groups, and regulatory bodies (ACC). Minimum Requirements Engineer III Minimum Requirements: - A ... studies, technical reviews, investigations and verifications. Complies with design, regulatory , operating and maintenance requirements. Ensures engineering analyses, design,… more
    Arizona Public Service (09/12/25)
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  • Medical Director, Gastrointestinal & Inflammation…

    Takeda Pharmaceuticals (Boston, MA)
    …the Company-wide patient safety expert for assigned pharmaceutical / biological / drug -device combined products, accountable for the safety strategy and major safety ... strategy for and lead preparation of responses to safety-related inquiries from regulatory agencies and ethics committees. + Ensure communication of all safety… more
    Takeda Pharmaceuticals (09/12/25)
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  • Fuels Product Management Leader - Nuclear

    GE Vernova (Wilmington, NC)
    …and ENUSA. **Cross-functional Leadership** + Collaborate with engineering, manufacturing, regulatory , finance and legal teams to align fuel product strategies ... Analysis** + Monitor global nuclear fuel market trends, geopolitical risks, and regulatory changes to guide product and investment decisions. + Work with Sourcing… more
    GE Vernova (09/12/25)
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  • Quality Improvement Specialist

    Banner Health (Glendale, AZ)
    …safety, harm reduction, clinical performance, peer review and compliance with regulatory and accrediting agencies. This is accomplished by utilizing performance and ... teams to improve processes that impact the safety of patients. 6. Regulatory and Accreditation - Supports the evaluating, monitoring, and improving compliance with… more
    Banner Health (09/11/25)
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  • Facility Security Officer

    GE Vernova (Niskayuna, NY)
    …Directives. The incumbent will serve as a technical expert in regulatory requirements, developing business policies, procedures, and training for the security ... + Partner with the Digital Technology Security Team to ensure regulatory compliance. + Perform as the site Communications Security (COMSEC) custodian.… more
    GE Vernova (09/11/25)
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  • Associate Director - US Public Policy

    Lilly (Washington, DC)
    …summaries, key arguments, and talking points in response to legislative and/or regulatory policies. + Maintain oversight of priority policy workstreams to ensure ... and related functions (Federal and State Government Affairs, Communications, Global Regulatory Policy, Global Patient Outcomes). + Other projects and duties as… more
    Lilly (09/09/25)
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  • Executive Medical Director, Clinical Development…

    AbbVie (North Chicago, IL)
    …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues. ... of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and other program documents. + In rare… more
    AbbVie (09/09/25)
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  • Lead Medical Director, Product Development,…

    Genentech (Boston, MA)
    …I & II protocols. + You have a demonstrated understanding of Phase II - III drug development. + You will take an active role with other CST members, regulatory ... and other internal partners/stakeholders in the completion and submission of regulatory filings and other regulatory documentation. Provides clinical science… more
    Genentech (09/06/25)
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