• Senior Manufacturing Technician

    Insight Global (Berkeley, CA)
    …with Biological Development and Tech Transfer teams. * Maintain GMP compliance, perform environmental monitoring, and ensure accurate documentation (Batch ... and Requirements * Manufacturing Experience: Hands-on experience in pharmaceutical or GMP -compliant manufacturing, ideally with exposure to cell therapy and upstream… more
    Insight Global (01/06/26)
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  • Senior Specialist, EHS

    Bristol Myers Squibb (Bothell, WA)
    …cleanroom manufacturing facilities, laboratories and outdoors at times and complies with GMP gowning and access requirements in these controlled areas. + Support the ... with urgency and agility. + Ability to comply with cleanroom and GMP manufacturing facility and laboratory gowning and entry requirements. + Experienced in… more
    Bristol Myers Squibb (01/03/26)
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  • Senior Researcher - Bioanalyst, RNA Therapeutics…

    Memorial Sloan-Kettering Cancer Center (New York, NY)
    …evaluation and characterization of RNA and LNP's for eventual tech transfer for GMP release. These assays will focus on the T-cell response to vaccines and ... _in vivo_ and _in vitro_ , focusing on T-cell responses, as well as GMP analytical release aligned with regulatory guidance and requirements + Assays will assess… more
    Memorial Sloan-Kettering Cancer Center (01/03/26)
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  • BMS/EMS (Automation) SME

    Insight Global (Gaithersburg, MD)
    …monitoring, data historian, alarm management) in line with AZ requirements and GMP . - Technical governance to the project delivery organization throughout the ... and environmental monitoring systems, ensuring design compliance with AZ standards, GMP , GEP, SHE, data integrity (ALCOA+), and computerized systems validation (CSV)… more
    Insight Global (01/03/26)
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  • Scientist III - Microbiologist, EM Focus,…

    Parexel (Topeka, KS)
    …**Required Skills and Experience** + Experience in working in a GMP Pharmaceutical environment with specific experience environmental monitoring + Proven technical ... submit equipment for calibrations (offsite or onsite) + Complete calibration/PM paperwork GMP ACTIVITIES: + Prepare GMP documentation as requested by management… more
    Parexel (01/02/26)
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  • QC Scientist II

    ThermoFisher Scientific (St. Louis, MO)
    …lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal ... QC Scientist II, you'll conduct complex analytical testing to support GMP manufacturing of biopharmaceutical products, from early-stage clinical development through… more
    ThermoFisher Scientific (01/01/26)
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  • Sr. Process Engineer (Aseptic Operation)

    CSL Behring (Kankakee, IL)
    …asset management strategies in alignment with ISO 55000 principles, GMP requirements, and business objectives, while partnering with Production, Maintenance, ... + Lead equipment-related changes through formal change control processes, ensuring GMP compliance, data integrity, and controlled risk. + Drive continuous… more
    CSL Behring (01/01/26)
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  • Machine Operator

    Aerotek (Windsor, WI)
    …commitment to maintaining high standards of quality and safety in a GMP environment. **Responsibilities** + Operate and maintain fermentation tanks and food ... and the ability to operate production machinery in a GMP environment with at least 1 year of experience....well-being. **Work Environment** You will work in a climate-controlled, GMP -compliant facility. The shifts are all 8 hours Mon-Fri.… more
    Aerotek (01/01/26)
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  • General Production Worker - PACK

    Aerotek (Defiance, OH)
    …our packaging line. You will be responsible for adhering to all food-related GMP and SOP guidelines, packing dry powdered contents for shipment, and ensuring product ... and maintaining sanitation practices of the equipment. **Responsibilities** + Follow all food-related GMP and SOP guidelines. + Pack items on the lines for shipment,… more
    Aerotek (01/01/26)
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  • Associate Director - TSMS Sterility Assurance

    Lilly (Pleasant Prairie, WI)
    …to influence and implement the technical agenda, site business plan objectives and GMP Quality Plan objectives + Technical review and approval for site GMP ... necessary changes to improve performance. + Review and approve GMP documentation including procedures, deviation investigations, technical reports, change controls,… more
    Lilly (01/01/26)
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