• Logistics Coordinator - 1st Shift

    Canon Business Process Services (New Albany, OH)
    …in a work environment focused on current Good Manufacturing Practices ( cGMP ). Responsibilities Logistics Coordinator I:* Maintains safe, clean and orderly work ... the client Quality Assurance team to ensure all materials and products meet cGMP and regulatory requirements. Logistics Coordinator II:* In addition to the above… more
    Canon Business Process Services (07/10/25)
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  • Manufacturing Technician II

    Takeda Pharmaceuticals (Round Lake Beach, IL)
    …II, you will implement all processes in production while strictly following cGMP , environmental health and safety guidelines and any applicable related regulations. ... + Receive and distribute supplies into the production area. + Follow cGMP , environmental health and safety guidelines, and any other regulations. + Complete… more
    Takeda Pharmaceuticals (07/05/25)
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  • Manager, Form/Fill Mon-Thurs, 8 PM - 6:30 AM

    Novo Nordisk (Bloomington, IN)
    …in accordance with regulatory, site, and client requirements. Manufacturing cGMP production activities include manual, semi-automated and automated inspection, ... in accordance with regulatory, site, and client requirements. Manufacturing cGMP production activities include solution preparation, master/working cell bank… more
    Novo Nordisk (07/05/25)
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  • Manufacturing Associate I

    Takeda Pharmaceuticals (Brooklyn Park, MN)
    …and document daily manufacturing operations according to SOPs in a cGMP environment. You will operate biologics production equipment (bioreactors, filtration units, ... systems and fixed/portable vessels + Perform basic trouble shooting + Document cGMP data for processing steps and equipment activities while following standard… more
    Takeda Pharmaceuticals (06/28/25)
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  • Sterile Manufacturing Technician

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    …the highest quality standards. - Maintain documentation and functional work areas to CGMP standards. - Capable of lifting and moving heavy equipment parts and ... good manual dexterity. - Must possess basic knowledge of CGMP -s. - Must be able to transcribe detailed data...be able to transcribe detailed data accurately according to CGMP and SOP standards. - Must be able to… more
    Glenmark Pharmaceuticals Inc., USA (06/14/25)
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  • Logistics Specialist II

    Fujifilm (College Station, TX)
    …for the accurate receiving, packing, shipping, and external distribution of cGMP (current Good Manufacturing Practices) and non-GMP materials in support of ... inventory system + Comply with safe handling and storage requirements, cGMP /ISO, local & corporate policies, and environmental/other related regulations + Perform… more
    Fujifilm (06/05/25)
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  • Director, External Manufacturing Compliance

    Regeneron Pharmaceuticals (East Greenbush, NY)
    …with quality compliance groups, strategically meet goals and lead External Manufacturing cGMP Policies and SOPs + Leads and prioritizes operations and practices for ... Regeneron audits + Provides expertise to the global External Manufacturing organization on cGMP compliance standard processes, as well as, new and developing cGMP more
    Regeneron Pharmaceuticals (06/01/25)
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  • Quality Assurance Associates I Or II - Open Pool

    Colorado State University (Fort Collins, CO)
    …includes the creation of development programs focused on implementing cGMP regulations and biomanufacturing production scalability. Position Summary The Quality ... is responsible for the implementation and execution of policies and procedures for the cGMP manufacturing of biologics. Individuals will be working within a cGMP more
    Colorado State University (05/30/25)
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  • Sr. Specialist I, Quality Assurance - Quality…

    Abeona (Cleveland, OH)
    …position supports the maintenance of the quality systems in support of a cGMP Operation for production processes relating to batch record review and release from ... that products are manufactured in compliance with site procedures, regulatory and cGMP guidelines. + Compile and verify all batch-related documents into a final… more
    Abeona (05/30/25)
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  • Quality Manager - Healthcare Business

    DuPont (Hemlock, MI)
    …healthcare market quality requirements (including Current Good Manufacturing Practice [ cGMP ] standards). This person will provide leadership while maintaining ... standards (eg: ISO-9001:2015, ISO-13485:2016, etc.) are implemented and maintained in accordance with cGMP (US 21 CFR 820) and FDA regulations. + Lead the overall… more
    DuPont (05/29/25)
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