• Manufacturing Compliance Specialist

    BioFire Diagnostics, LLC. (Durham, NC)
    …for this role are anticipated to be Friday - Sunday 7:00am - 7:30pm. The Manufacturing Compliance Specialist will focus on Right First Time (RFT) initiatives + ... Review of manufacturing documentation for compliance to GDP and CPP prior...track batch record turnaround time, errors and document related deviations + Track training activities and curriculums to ensure… more
    BioFire Diagnostics, LLC. (01/10/25)
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  • Quality Assurance Area Specialist II - API

    Novo Nordisk (Clayton, NC)
    …of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable ... products. At API, you'll join a global network of manufacturing professionals who are passionate about what they do....of batch reports for release of API materials, minor deviations , minor change controls, review & approval of SOPs,… more
    Novo Nordisk (01/15/25)
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  • Senior Quality Assurance Area Specialist I

    Novo Nordisk (Clayton, NC)
    …of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable ... products. At API, you'll join a global network of manufacturing professionals who are passionate about what they do....review of batch reports & release of API materials, deviations , change controls, review & approval of SOPs, QA… more
    Novo Nordisk (01/15/25)
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  • Quality Assurance Area Specialist III

    Novo Nordisk (Clayton, NC)
    …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 Product Supply Aseptic Manufacturing (PS AM) facility in Clayton, NC is a...inspections. Review & approval of complex Change Requests (CR's), Deviations (DVs), CAPAs & other documentation. Performs Self Audits… more
    Novo Nordisk (01/18/25)
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  • Quality Assurance Area Specialist I…

    Novo Nordisk (Clayton, NC)
    …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 Product Supply Aseptic Manufacturing (PS AM) facility in Clayton, NC is a...for Quality review & approval of Change Requests (CR's), Deviations & other documentation. Perform Self Audits (in conjunction… more
    Novo Nordisk (01/16/25)
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  • HSE Specialist (Health, Safety,…

    Lilly (Durham, NC)
    …This is an exciting opportunity to help build and operate a state-of-the-art manufacturing site from the ground up. The Health, Safety, Environmental (HSE) ... Specialist will be responsible for the development and technical...+ Experience with CAPA system for HSE changes and deviations + Demonstrated technical leadership skills + Strong communication… more
    Lilly (01/03/25)
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