• Sr. IT Engineer 1, CSV

    Fujifilm (Holly Springs, NC)
    …strategies and procedures. This role facilitates improvement initiatives, supports regulatory agency, and third-party inspections, as needed. **Company Overview** ... North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.… more
    Fujifilm (08/11/25)
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  • Lead Engineer - Plant Civil and Structural

    GE Vernova (Wilmington, NC)
    …and external customers, suppliers, partners, licensing, the NRC and international regulatory authorities on technical issues + Incorporate design requirements into ... upon the successful completion of a background investigation. The drug screen requirement in the background check process is...plan or program. This document does not create a contract of employment with any individual. \#LI-DY1 _This role… more
    GE Vernova (07/30/25)
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  • Principal Engineer - Electrical Power System…

    GE Vernova (Wilmington, NC)
    …risk analysis (PRA), and similar techniques. + Support nuclear regulatory certification or licensing document preparation, + Perform technical oversight, ... upon the successful completion of a background investigation. The drug screen requirement in the background check process is...plan or program. This document does not create a contract of employment with any individual. \#LI-DS6 #LI-Remote _This… more
    GE Vernova (07/29/25)
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  • Technical Leader - Civil Structural Engineering

    GE Vernova (Wilmington, NC)
    …and external customers, suppliers, partners, licensing, the NRC and international regulatory authorities on technical issues + Incorporate design requirements into ... upon the successful completion of a background investigation. The drug screen requirement in the background check process is...plan or program. This document does not create a contract of employment with any individual. \#LI-DS6 #LI-Remote _This… more
    GE Vernova (07/29/25)
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  • FEMA - Scientific Specialist

    CDM Smith (Greensboro, NC)
    …laws and executive orders. * Assists FEMA with consulting with regulatory agencies and preparing environmental documents such as Environmental Assessments. * ... to change quickly and remain flexible. **Background Check and Drug Testing Information:** CDM Smith Inc. and its divisions...to announce that CDM Smith won the next 5-year contract for Public Assistance Technical Assistance Contractors - PA… more
    CDM Smith (07/19/25)
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  • FMO Manufacturing Maintenance Supervisor

    GE Vernova (Wilmington, NC)
    …of employment is conditional upon the successful completion of a background investigation and drug screen + Must be 18 years or older and have legal authorization to ... + Knowledge of nuclear fuel manufacturing + Experience working in Nuclear Regulatory Commission (NRC) regulated environment + Ability to read and interpret… more
    GE Vernova (07/04/25)
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  • Quality Associate II/III (2nd Shift)

    Grifols Shared Services North America, Inc (Clayton, NC)
    …should also have basic knowledge/understanding of domestic (ie Food and Drug Administration) and applicable foreign regulatory agency requirements/guidelines. ... may also include those associated with release and shipment of Contract Fractionation batches and Quarantine of intermediates. **Responsibilities include:** +… more
    Grifols Shared Services North America, Inc (08/26/25)
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  • Asset & Configuration Management Lead

    CRC Insurance Services, Inc. (Charlotte, NC)
    …analysis. + Support audit and compliance activities, including internal controls and regulatory requirements. + Manage vendor relationships and contract records ... drive decisions and process improvements. + Familiarity with audit, compliance, and regulatory frameworks relevant to IT asset management (eg, SOX, HIPAA, GDPR) is… more
    CRC Insurance Services, Inc. (08/26/25)
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  • Senior Director, Clinical Trials Management

    Sumitomo Pharma (Raleigh, NC)
    …study documents and plans to ensure adequate controls, aligning with GCP and regulatory requirements for study conduct. They will provide expert input into study ... oversight in the selection, training, and management of study personnel, Contract Research Organizations (CROs), and other vendors, ensuring they meet project… more
    Sumitomo Pharma (08/21/25)
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  • Engineer - Engineering Tech Center - Parenteral…

    Lilly (Durham, NC)
    …to effectively guide and support Lilly's partner companies and contract manufacturers. _Key Objectives/Deliverables_ + Technical and Discipline leadership -Partners ... Compliance - Ensure personal and team compliance with all applicable regulatory and corporate policy requirements; ensure appropriate safety practices and procedures… more
    Lilly (08/16/25)
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