• Manufacturing Specialist II - Cell Therapy

    Kelly Services (Winston Salem, NC)
    …improvement initiatives, including incident investigations and procedural enhancements. + Perform aseptic processes in a cleanroom environment following sterile ... + Strong ability to lead by example, troubleshoot processes, and uphold cGMP and aseptic standards. + Experience operating manufacturing equipment and… more
    Kelly Services (07/30/25)
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  • Specialist I, Form/Fill (Weekend PM Shift for SL3)

    Novo Nordisk (Bloomington, IN)
    …what matters. Primary - Drug Product Primary Manufacturing produces sterile pharmaceuticals. The department includes equipment preparation, product formulation, ... material staging, and aseptic filling. Product in this area is filled into...area is filled into vials, syringes, or cartridges inside sterile isolator barriers. The sterile barrier isolator… more
    Novo Nordisk (06/12/25)
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  • Sr. Maintenance Technician

    Merck (Durham, NC)
    …troubleshooting and maintenance support to VMF Operations areas ( sterile supply, weigh/dispense, media, stabilizer/prep, thaw/pool, filling, capping/inspection, ... clean utilities etc.) located in aseptic and clean room environments. Works within a team...osmosis skids, vapor compression stills, compressed gas systems + GMP production related equipment (eg Autoclaves, Fillers, Lyophilizers, Cappers… more
    Merck (07/31/25)
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  • Cell Therapy Specialist

    Actalent (Frederick, MD)
    …attention to detail, and troubleshooting skills to complex manufacturing issues + Sterile gowning and aseptic processing qualifications in previous positions ... clinical material as part of a team in a GMP environment. + Provide expert consultation on tech transfer...problems during cell therapy product manufacturing. + Comply with cGMP standards and good documentation practices; timely review executed… more
    Actalent (08/02/25)
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  • Cell Therapy Specialist

    Actalent (Frederick, MD)
    …experience in cGMP production of biologics, preferably cell therapy. + Sterile gowning and aseptic processing qualifications. Work Environment This role ... role in the production of cutting-edge cell therapy products in a GMP environment. Responsibilities + Execute manufacturing batch records and standard operating… more
    Actalent (07/30/25)
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  • Microbiology Associate Scientist

    Unither Pharmaceuticals (Rochester, NY)
    …With 30 years of technological expertise, we position ourselves as a world leader in sterile single dose with 10 sites on 4 continents and more than 2000 employees. ... manufacturing and packaging operations using suitable instrumentation according to cGMP 's. Supports laboratory to ensure laboratory procedures, equipment, supplies,… more
    Unither Pharmaceuticals (07/18/25)
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  • Principal Engineer, Equipment Process

    Catalent Pharma Solutions (Harmans, MD)
    …technology; + Familiarity with cGMPs, regulatory filings, and compliance issues for sterile injectable products manufactured by aseptic processing; + Knowledge ... **Principal Engineer, Equipment Aseptic Filling** **Position Summary:** Catalent, Inc. is a...of quality and service. Catalent provides process development and GMP manufacturing services for Phase I/II clinical trials to… more
    Catalent Pharma Solutions (06/26/25)
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  • Validation Analyst II

    Curia (Albuquerque, NM)
    …conversational noise in the background. The pharmaceutical manufacturing environment is sterile . Therefore, aseptic gowning is required. Personal protective ... equipment, processes, utilities, systems, and components in alignment with cGMP regulations, internal procedures, and applicable regulatory expectations. This… more
    Curia (08/08/25)
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  • Manufacturing Specialist

    Curia (Albuquerque, NM)
    …and vial sealing) of parenteral products according to Current Good Manufacturing Practice ( cGMP ) in an aseptic environment. This role will train, coach/develop, ... enhance production processes and efficiency. The position also involves sanitizing aseptic and controlled areas using specialized solutions and equipment, following… more
    Curia (06/19/25)
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  • Quality Deviation Investigator III

    Curia (Albuquerque, NM)
    …produce sterile quality products + Document information, events, and cGMP manufacturing processes, accurately and completely + Perform duties in an organized, ... conversational noise in the background. The pharmaceutical manufacturing environment is sterile . Therefore, aseptic gowning is required. Personal protective… more
    Curia (06/26/25)
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