• Manufacturing Team Lead, Liso-cel CAR-T,…

    Bristol Myers Squibb (Summit, NJ)
    …components per Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing ... purification, and aseptic processing or lab technique. + Knowledge of cGMP /FDA regulated industry. + Basic mathematical skills. + General understanding of… more
    Bristol Myers Squibb (10/16/25)
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  • Senior Specialist, Quality Assurance

    Cardinal Health (Trenton, NJ)
    …documentation in accordance with current Good Manufacturing Practices ( cGMP ), FDA regulations, and internal procedures. **_Responsibilities_** **Labeling Review ... in related field, or equivalent work experience, preferred + Working knowledge of cGMP and FDA regulations. + Experience with quality management systems and labeling… more
    Cardinal Health (10/15/25)
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  • Equipment Engineer

    System One (Warren, NJ)
    …of calibration and maintenance plans in site CMMS system. * Follows cGMP (current Good Manufacturing Practices) and ALCOA principles ('ALCOA' defines that data ... Complete, Consistent, Enduring, and Available. Qualifications: + Knowledge of cGMP and good documentation practices. + Knowledge of pharmaceutical, manufacturing… more
    System One (10/14/25)
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  • Production Associate

    Aerotek (Piscataway, NJ)
    …during the 1st shift for one week. **Responsibilities** + Follow all safety and cGMP guidelines as outlined in the company's Food Safety and Quality Programs. + ... checks and traceability. **Essential Skills** + Knowledge of production processes and cGMP guidelines. + Experience with filling machines and quality standards. +… more
    Aerotek (10/14/25)
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  • Senior Director, MSAT Biologics

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …recommending and implementing innovations where appropriate + Ensure compliance with cGMP regulations and other relevant quality standards + Represent the MSAT ... scale-up, and technology transfer of biologics products + Strong knowledge of cGMP regulations and ICH guidelines relevant to biologics manufacturing + Experience… more
    Otsuka America Pharmaceutical Inc. (10/13/25)
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  • Mechanic Operator, CSO

    Bristol Myers Squibb (New Brunswick, NJ)
    …the pharmaceutical industry. + Individual must have a minimum of five-year's applicable CGMP experience in the pharmaceutical industry. + Proficiency in the use of ... repetitive; requiring application of judgement within limitations established by CGMP regulations, defined SOP's and processing instructions. Required to document… more
    Bristol Myers Squibb (10/12/25)
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  • Clinical Packaging Operator Technician

    Bristol Myers Squibb (New Brunswick, NJ)
    …repetitive, requiring application of judgement within limitations established by CGMP regulations, defined SOP's and processing instructions. Required to document ... lieu of a two-year degree a minimum four years applicable experience within a CGMP regulated industry will meet requirements. + Proficiency in the use of computer… more
    Bristol Myers Squibb (10/10/25)
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  • Quality Control Technician

    Lilly (Branchburg, NJ)
    …as assigned by Supervisor. Performs routine QC responsibilities as needed. Applies cGMP practices during the execution of all work tasks. Exhibits strong teamwork ... Attentive to detail. 3. Good teamwork and communication skills. 4. Exposure to cGMP regulations and work experience in a regulated environment are preferred. 5.… more
    Lilly (10/09/25)
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  • Quality Control Scientist - Microbiology,…

    Catalent Pharma Solutions (Princeton, NJ)
    …our European Center of Excellence for cell therapy in Gosselies, Belgium. The CGMP manufacturing facility is equipped with 16 flexible clean rooms, QC labs, and ... + Maintain compliance with SOPs and regulatory requirements (FDA, EMA, cGMP ) by documenting results, supporting audits, and ensuring equipment calibration and… more
    Catalent Pharma Solutions (10/04/25)
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  • Senior Scientist, Crystallization Lab Engineering…

    Merck (Rahway, NJ)
    …drug substance/drug product interface. + Familiarity with concepts and application of cGMP during pharmaceutical development and production. + A high level of ... . PRD \#eligibleforERP \#WE25 **Required Skills:** Adaptability, Adaptability, Bioreactors, cGMP Regulations, Chemical Biology, Chemical Engineering, Chemical Technology, Chromatographic… more
    Merck (10/01/25)
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