• Senior Manager, GMP Facilities

    Bristol Myers Squibb (Summit, NJ)
    …place than here at BMS with our Cell Therapy team. The Senior Manager, GMP Facilities provides leadership and direction to the 24/7 Facilities and Maintenance team ... Department. This team is responsible for ensuring that the Summit West GMP manufacturing facilities and supporting equipment are operated and maintained to ensure… more
    Bristol Myers Squibb (12/03/25)
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  • Associate Director, Global Product Quality…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    **Job Summary** The Associate Director, Global Product Quality - GMP Process is responsible for enabling the optimization and harmonization of key GMP quality ... leadership, coaching, and subject matter expertise to global teams on GMP compliance and quality system execution. **Qualifications** Required + Bachelor's degree… more
    Otsuka America Pharmaceutical Inc. (12/10/25)
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  • GMP Cleaner

    ABM Industries (Millburn, NJ)
    **Overview** **Job Summary Details:** **Job Summary Details:** The GMP Cleaner is responsible for the support activities and disinfection of GMP space, equipment ... and associated areas involved in production facilities within the manufacturing, R&D, warehousing, and final product fill areas according to current Good Manufacturing Practices (cGMPs). **Pay: $23.00 PER HOUR** + The pay listed is the hourly range or the… more
    ABM Industries (12/04/25)
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  • GMP Manufacturing Equipment Supervisor

    System One (Cranbury, NJ)
    Job Title: GMP Manufacturing Equipment Supervisor Location: Cranbury, NJ Hours / Schedule: M-F; some flexibility with start time; 8am - 5pm Type: Contract to Hire ... understanding of mechanical, electrical, and facility systems in a GMP -regulated environment. + Strong working knowledge of OSHA regulations, Lockout/Tagout,… more
    System One (10/18/25)
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  • Technician, Filling Operations (Onsite)

    Merck (Rahway, NJ)
    …Laboratory, and Experimentation (FLEx) Center to support drug product development and GMP clinical supply of sterile dosage forms. Positions will support development ... feedback on product and process development. These roles require adherence to GMP procedures, strong attention to detail in completing GMP documentation,… more
    Merck (12/13/25)
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  • Senior Manager, Global Product Quality - Biologics

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …way that is in accordance with regulatory expectations and applicable GMP /GDP quality standards. This role will provide specialized Biologics Quality Assurance ... and downstream biologics manufacturing processes, ensuring compliance with biologics-specific GMP requirements. This role has global responsibility for managing… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Senior Technician, Filling Operations (Onsite)

    Merck (Rahway, NJ)
    …Laboratory, and Experimentation (FLEx) Center to support drug product development and GMP clinical supply of sterile dosage forms. Positions will support development ... feedback on product and process development. These roles require adherence to GMP procedures, strong attention to detail in completing GMP documentation,… more
    Merck (12/13/25)
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  • Principal Engineer, Assay and Data Automation

    Bristol Myers Squibb (Warren, NJ)
    …strong technical background in automation design, development, and deployment within both GMP and non- GMP labs. This individual will foster effective ... automation platforms for bio-analytical methods that are performed in GMP and non- GMP labs. + Effectively communicate experimental results to influence program… more
    Bristol Myers Squibb (12/06/25)
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  • Senior Engineer, Automation

    Merck (Rahway, NJ)
    …both in terms of facility construction and organizational realization. The GMP facility is designed for multi-product operations with flexible operating suites, ... trialing new automation strategies, and implementing them in the GMP areas + Support capital projects, work to design,...to design, install, and qualify new equipment to support GMP clinical production. Write, review or execute test documents.… more
    Merck (12/05/25)
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  • Facilities Technician- Biopharma/Pharma Industry

    Astrix Technology (New Brunswick, NJ)
    …in maintaining and supporting facility and equipment operations within a GMP biotechnology manufacturing environment. This position is responsible for both facility ... preventive maintenance, troubleshooting, and repair activities, while maintaining full GMP compliance and documentation standards. **Location:** Middlesex County, NJ… more
    Astrix Technology (12/10/25)
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