• Scientist - Analytical Chemistry

    Actalent (Sanford, NC)
    …Scientist - Analytical to join the Quality Control Method Transfer and Validation (MTV) team. This role supports high-impact projects in vaccine and monoclonal ... + Independently design, plan, and execute laboratory experiments + Perform method validation , assay development, and method transfer + Draft and review protocols,… more
    Actalent (07/24/25)
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  • Quality Representative - Floor Support Parenteral

    Lilly (Concord, NC)
    …revisions. **Basic Requirements:** + Bachelors degree + Quality knowledge in pharmaceutical manufacturing required + Previous experience with C&Q / Verification and ... Validation oversight including automation and computer systems validation + Proficiency with computer systems including Microsoft office products, Trackwise… more
    Lilly (06/24/25)
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  • Scientist II, Manufacturing Sciences - Continuous…

    ThermoFisher Scientific (Greenville, NC)
    …**Key Responsibilities:** + Collaborate with cross-functional teams-including validation , operations, quality, analytical development, and process development-to ... and review batch records, protocols, and reports to support development, validation , and commercial production activities. + Support routine manufacturing operations… more
    ThermoFisher Scientific (06/18/25)
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  • PAT Scientist III

    ThermoFisher Scientific (Greenville, NC)
    …Description** **As a Manufacturing Scientist, you will contribute to the development, validation , and optimization of chemometric models for oral solid dosage (OSD) ... owner for assigned products. **Education** Bachelor's degree in Chemical Engineering, Pharmaceutical Sciences, Chemistry, Data Science, or a related field is… more
    ThermoFisher Scientific (06/18/25)
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  • Senior Associate Quality Control, Environmental…

    Amgen (Holly Springs, NC)
    …to: SOPs, protocols, safety assessments, methods, trend reports, qualification/ validation summary reports, microorganism assessments, technical reports, and method ... degree **Preferred Qualifications:** + Experience working in a GMP pharmaceutical production facility with classified areas and applicable gowning requirements.… more
    Amgen (06/12/25)
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  • Associate Director, Clinical Laboratory

    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 ... functioning properly, monitoring patient and quality control testing results, planning, validation and implementation of new test procedures in collaboration with… more
    GRAIL (05/20/25)
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  • Manager, PVRM

    Sumitomo Pharma (Raleigh, NC)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... + Assist in signal detection activities including data assembly, signal validation , and signal evaluation. + Perform literature monitoring (with vendor support)… more
    Sumitomo Pharma (08/01/25)
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  • Manager, Maintenance (Reliability) Engineering

    Novo Nordisk (Clayton, NC)
    …for millions of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our ... injectable and oral treatment supply chains. Our newer Active Pharmaceutical Ingredients (API) facility in Clayton, NC sits on 825,000 square-feet of… more
    Novo Nordisk (07/29/25)
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  • Senior Packaging Maintenance Mechanic

    Merck (Wilson, NC)
    …Maintenance Coach, sets up, adjusts, repairs, and maintains all pharmaceutical process equipment. Performs calibrations and maintains industrial instrumentation ... developing/performing PM's, developing/performing instrument calibrations, installing new equipment, completing validation protocols, documenting work using a computerized maintenance management… more
    Merck (07/29/25)
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  • Associate Director, Commercial Quality Assurance

    Catalent Pharma Solutions (Greenville, NC)
    …Candidate** + PhD with at least 7 years of professional experience in QA/QC pharmaceutical manufacturing or; + Master's degree with at least 9 years of professional ... experience in QA/QC pharmaceutical manufacturing or; + Bachelor's degree with 10 years...cross-functional teams, such as Technical Services, facilities, Engineering and Validation . + Demonstratable leadership experience at Catalent (including but… more
    Catalent Pharma Solutions (07/29/25)
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