• Quality Documentation Specialist

    US Tech Solutions (Wilson, NC)
    …related to the storage and archiving of documents related to BioNC including validation documents + Prepares and catalogues documents for archival + Coordinates with ... in document management or related role within the biological and/or pharmaceutical industry + Knowledgeable of FDA/EMEA regulatory requirements applicable to… more
    US Tech Solutions (08/13/25)
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  • Sr. Quality Associate I

    Grifols Shared Services North America, Inc (Clayton, NC)
    …and Annual Product Reviews as well as providing Quality input for Validation projects, Regulatory submissions and audits. The incumbent will be responsible for ... computer skills include Excel, Word and SAP. Experience in different aspects of pharmaceutical business is a plus. Requirements: M8: BS/BA degree preferably in a… more
    Grifols Shared Services North America, Inc (08/13/25)
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  • FSP Senior Epidemiologist (Inflammation)

    IQVIA (Durham, NC)
    …and evaluate key variables, including diagnosis and procedures codes, and plan validation studies as needed + Conduct analyses for descriptive and comparative ... four (4) years of relevant post-doctoral experience, preferably in pharmaceutical industry, biotechnology, or consulting environment. Master's degree in epidemiology… more
    IQVIA (08/08/25)
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  • Associate Medical Director/Med Dir - Neurology

    ThermoFisher Scientific (Wilmington, NC)
    …sites. + Performs data review as specified in the client contract and data validation manual including review of coding listings and/or full safety data to assess ... following: + Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years)… more
    ThermoFisher Scientific (08/08/25)
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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 (08/08/25)
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  • Field Applications Scientist, Immunoassay…

    Bio-Techne (Raleigh, NC)
    …Education and Experience: + Minimum BS/BA degree in biochemistry, bioengineering, pharmaceutical sciences, biology or a related life science field. MS/PhD and ... fields + Independently execute assay and reagent troubleshooting, optimization and validation experiments + Excellent oral and written communication skills, to… more
    Bio-Techne (08/08/25)
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  • CLIA Laboratory Director (Board Certified…

    GRAIL (Durham, NC)
    …United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com ... for new test development + Review and approves the technical performance validation and verification reports for new tests, instruments, and methods prior to… more
    GRAIL (07/22/25)
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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 ... + 2+ years prior experience in manufacturing operations, preferably in pharmaceutical , food, or cosmetic industry. + 2+ years supervisory/leadership experience… 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 ... and SME support. **Basic Requirements:** + Minimum 3 years in the pharmaceutical industry with specific data stewardship experience. + On-site presence required.… more
    Lilly (07/18/25)
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  • Senior Scientist Regulatory Compliance

    Cambrex High Point (High Point, NC)
    …necessary Qualifications/Skills + Knowledge and Experience in Computer System Validation (CSV). + Knowledge of Electronic Quality Management/Document Systems ... least 3 years of relevant background/leadership in GXP/QA/regulatory compliant pharmaceutical laboratory environment or Quality Assurance/Regulatory Affairs role (prefer… more
    Cambrex High Point (07/17/25)
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