• Associate Director, Commercial Quality Assurance

    Catalent Pharma Solutions (Greenville, NC)
    …continuous improvement philosophy focused on improved compliance, right-first-time and process efficiency while creating an environment of open communication, ... 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… more
    Catalent Pharma Solutions (07/29/25)
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  • Facilities Engineer I - Black Utilities API

    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 (07/25/25)
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  • Sterility Assurance Manager

    ThermoFisher Scientific (Greenville, NC)
    …of aseptic process simulations (media fills). + Experience with pharmaceutical industry technology, especially from a validation , technical or laboratory ... Laboratory or Environmental Monitoring experience, and ideally within a sterile pharmaceutical manufacturing facility). + Experience in a pharmaceutical quality… more
    ThermoFisher Scientific (07/19/25)
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  • Director, Manufacturing Science and Technology

    ThermoFisher Scientific (Greenville, NC)
    …and own lab experiments + Post PPQ, full ownership of all continuous process validation activities + Lead and coordinate large-scale technical projects from ... Drug Products and directs a team of Molecular Biologists, Chemical & Process Engineers, and Scientists. This team leads strategic, tactical and operational technical… more
    ThermoFisher Scientific (07/13/25)
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  • Automation Manager

    Pfizer (Rocky Mount, NC)
    …such as MS Word, Excel, PowerPoint. + Broad experience in a pharmaceutical environment with a hands-on understanding of control and data acquisition systems, ... Have (Preferred Requirements)** + Prior experience in a high regulated pharmaceutical or biotech manufacturing environment. + Demonstrated experience in project… more
    Pfizer (07/30/25)
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  • 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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  • Senior Associate Quality Control, Environmental…

    Amgen (Holly Springs, NC)
    …support of Amgen North Carolina commercial product release. Scope includes in- process , release, stability and routine monitoring testing. The Senior Associate ... limited to: SOPs, protocols, safety assessments, methods, trend reports, qualification/ validation summary reports, microorganism assessments, technical reports, and method… more
    Amgen (06/12/25)
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  • Quality Control Lab Services Manager

    J&J Family of Companies (Wilson, NC)
    …lifecycle management including Analytical Instrument Qualification (AIQ) and Computer System Validation (CSV), among others. + Perform budget support as the point ... + Minimum of 6 years of experience working within the biological and/or pharmaceutical industry. + Experience in a Quality leadership role. + Experience working with… more
    J&J Family of Companies (07/17/25)
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  • Technician - Sterility Assurance TSMS (Night…

    Lilly (Durham, NC)
    …Parenteral Facility. As designated by management, additional support for qualification/ validation activities or other routine responsibilities within the TS/MS group ... including the execution of required studies. + Execute or assist in qualification/ validation activities to support the bioburden control of the facility or equipment… more
    Lilly (07/18/25)
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  • Principal Scientist - Tsms Par

    Lilly (Concord, NC)
    …on the delivery of parenteral operations, specifically regarding technical transfer and process validation . TSMS PAR Scientist will support the formulation, ... ensure a state of capability and control, harmonization of control strategies across process teams, evaluate process improvement, and serving as an escalation… more
    Lilly (07/30/25)
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