• Lead Engineer, CSV

    Bristol Myers Squibb (Summit, NJ)
    …Completes all qualification and validation documentation with accuracy, completeness, and compliance to BMS standards. + Independent ownership of all lifecycle ... site customers while promoting a positive learning, team environment. + Author quality procedures and training documents. + Deliver training on procedures and best… more
    Bristol Myers Squibb (11/22/25)
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  • Pharma Technical Writer

    System One (New Brunswick, NJ)
    …business hours) Compensation: $34.87- $44.29 Type: Contract Overview Leading pharmaceutical company looking for an experienced Technical Writer. Ideal candidates ... of experience specifically for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. Responsibilities + Co-authors/ authors scientific… more
    System One (09/23/25)
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  • Validation Engineer III

    AbbVie (Branchburg, NJ)
    …skills with demonstrated ability to work within a team environment. + Knowledge of quality / compliance management as well as regulations and standards affecting ... facilities, utilities, product, processes etc.in line with project, operations and quality objectives. Level of responsibility and performance is commensurate with… more
    AbbVie (09/30/25)
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  • Director, Global Trial Lead

    Bristol Myers Squibb (Madison, NJ)
    …oversight for multiple, complex clinical trials and programs, ensuring delivery of high- quality data and regulatory compliance . + Spearheads collaboration with ... clinical trials with expertise in planning, execution, and oversight. Ensures regulatory compliance , patient safety, and timely delivery of high- quality data.… more
    Bristol Myers Squibb (11/25/25)
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  • Sr. Corporate Counsel & Chief Privacy Officer

    Terumo Medical Corporation (Somerset, NJ)
    …Corporation (TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high- quality medical devices used in a broad range of applications for ... programs that drive clear economic value, better clinical outcomes and improved quality of life for patients. TMC is part of Tokyo-based Terumo Corporation;… more
    Terumo Medical Corporation (11/25/25)
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  • Senior Vaccine Customer Representative - Richmond…

    Merck (Trenton, NJ)
    …health care providers such as physicians, nurses, pharmacists as well as quality directors, immunization managers, and office managers. Within their geography there ... patient health outcomes, customer feedback, marketplace dynamics, and progress towards quality goals. + Providing customers with key insights by keeping apprised… more
    Merck (11/22/25)
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  • Manager, R&D Applications

    Sumitomo Pharma (Trenton, NJ)
    Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the US (Sumitomo Pharma America, Inc.), focused on addressing patient ... from implementation to ongoing optimization + Lead and initiate troubleshooting quality and/or functionality issues associated with technology systems in scope +… more
    Sumitomo Pharma (11/15/25)
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  • Scientist II

    Sumitomo Pharma (Trenton, NJ)
    Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the US (Sumitomo Pharma America, Inc.), focused on addressing patient ... and biomarker studies conducted with CROs and academic investigators to ensure high- quality , timely delivery of data + Maintain organized, detailed logs of studies… more
    Sumitomo Pharma (11/05/25)
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  • Calibration and Metrology Technician

    ThermoFisher Scientific (Teterboro, NJ)
    …to patients around the world. The Ridgefield site exemplifies our commitment to quality , patient-safety and innovation in the pharmaceutical industry, making a ... and repairing complex utility systems, providing technical support, ensuring compliance with documentation and safety standards, and responding to high-priority… more
    ThermoFisher Scientific (09/04/25)
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  • QC Lab Supervisor- Full Benefits

    Kelly Services (Princeton, NJ)
    …to Hire- Princeton NJ The **QC Chemistry Supervisor** will lead all Quality Control Chemistry laboratory operations to support GMP manufacturing, testing, and ... release of raw materials, intermediates, and finished products in compliance with FDA, EU, and international regulatory standards. **Key Responsibilities:** + Lead… more
    Kelly Services (11/29/25)
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