• Senior Scientist Regulatory Compliance

    Cambrex High Point (High Point, NC)
    …filings. + Provide regulatory feedback on new and existing raw material, in- process and product specifications and test methods. + Provide feedback and/or lead ... resolve them. + Manage and carry out product quality review and continued process verification programs. Compile data from paper and electronic sources to complete… more
    Cambrex High Point (07/17/25)
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  • Automation Engineer 2, MES (Syncade)

    Fujifilm (Holly Springs, NC)
    …such as code configuration, document development, and test execution within several process areas + Delivers accurate and on-time Automation work + Creates standard ... + Collaborates with other departments, such as Manufacturing, Maintenance, and Validation + Other duties, as assigned **Knowledge and Skills** + Effective… more
    Fujifilm (06/27/25)
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  • Medical Science Liaison - South Atlantic

    Teva Pharmaceuticals (Raleigh, NC)
    …will be provided if an employee receives an offer of employment. **Reports To** In process of validation **Already Working @TEVA?** If you are a current Teva ... is highly preferred Minimum 1 year of experience working in pharmaceutical industry Experience in delivering effective and influential oral presentations Experience… more
    Teva Pharmaceuticals (07/24/25)
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  • Senior Automation Engineer - BAS Lead

    J&J Family of Companies (Wilson, NC)
    …team professionals with various technical expertise, responsible for the implementation, validation , qualification and maintenance of the ISA-95 level 1 and 2 ... PLCs. + Project Management experience **Preferred:** + Experience in a pharmaceutical or GMP-regulated manufacturing environment. + In-depth technical knowledge of… more
    J&J Family of Companies (07/25/25)
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  • QA Supervisor, Batch Release

    ThermoFisher Scientific (Greenville, NC)
    …manufacturing audits, record review, final product release functions, complaints, APR, validation , and investigations. + Quality Assurance: Ensure the quality of ... through coordination and review of operations, staff training, and system/ process improvements. + Technical Expertise: Provide technical expertise for systems… more
    ThermoFisher Scientific (07/20/25)
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  • Quality Assurance - Data Steward

    Lilly (Durham, NC)
    …of the establishment of site master data. + Support the implementation, validation and maintenance of the software based computerized quality systems for the ... support. **Basic Requirements:** + Minimum 3 years in the pharmaceutical industry with specific data stewardship experience. + On-site...to request an accommodation as part of the application process and any other correspondence will not receive a… more
    Lilly (07/18/25)
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  • Lab Analyst

    ManpowerGroup (Rocky Mount, NC)
    …to extend/convert) **What's the Job?** + Perform basic analysis for raw materials, in- process , finished products, and validation testing in a safe and compliant ... Our client, a leader in the pharmaceutical industry, is seeking a Lab Analyst to join their team. As a Lab Analyst, you will be part of the Quality Control… more
    ManpowerGroup (06/17/25)
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  • Manufacturing Systems Engineer

    Amgen (Holly Springs, NC)
    …a manufacturing environment with 2+ years of demonstrated ability in the Pharmaceutical or Biotechnology industries. + Experience in Automation Platforms such as but ... methodologies and 21 CFR Part 11. + General experience with computer validation and change control methodology. + Experience with computerized systems including… more
    Amgen (06/05/25)
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  • Associate 2, QC Microbiology (Sunday- Wednesday…

    Fujifilm (Research Triangle Park, NC)
    …direction of management * Assists with laboratory equipment qualification and validation activities * Participates in project developments from concept through ... 6 years of Microbiology experience; or * Associate's degree in Life Science, Pharmaceutical , or related field with 2-4 years of Microbiology experience; or *… more
    Fujifilm (05/07/25)
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