• Director , Global Quality

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    The Director , Global Product Quality , GMP Processes is a strategic leadership role responsible for **benchmarking, standardizing, and optimizing ... continuous improvement** across all regions and product lines. The Director will lead global initiatives to harmonize...operational efficiency. + GMP Compliance: Ensure all quality processes meet global regulatory requirements (eg,… more
    Otsuka America Pharmaceutical Inc. (12/16/25)
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  • Associate Director , Global Product…

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    **Job Summary** The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial ... product integrity while optimizing operational efficiency. + Works collaboratively within the Global Quality Dept. and other functions within OAPI and OPDC… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Associate Director , Global Product…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    **Job Summary** The Associate Director Controlled Substances, Quality Global Product Quality - API/DP is responsible for directing quality oversight ... and final finished product) for controlled substances + Works collaboratively within the Global Quality Dept. and other functions within OAPI and OPDC to… more
    Otsuka America Pharmaceutical Inc. (12/19/25)
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  • Associate Director , Global Supplier…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    The Associate Director of Global Supplier Quality will be responsible for the execution of supplier quality audit and monitoring across the company's ... + **Compliance & Documentation** + Ensure supplier compliance with global regulatory requirements (eg, FDA, EMA, ICH). + Prepare..., with 2+ years in supplier or external manufacturing quality . + Strong knowledge of GMP regulations… more
    Otsuka America Pharmaceutical Inc. (12/16/25)
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  • Director , Global Packaging…

    Merck (Rahway, NJ)
    **Job Description** The Global Packaging Procurement Director is responsible to lead the Packaging Center of Excellence (COE) organization. The scope for this ... support overall category management for the packaging category led by the global COE's, either directly (for local managed categories) or indirectly through strong… more
    Merck (12/18/25)
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  • Director , Technical Operations…

    Merck (Rahway, NJ)
    **Job Description** The Director , Technical Operations within Global Clinical Supply (GCS) is responsible for technical leadership in support of GCS global ... equipment-based challenges when required. The technical lead may also manage global infrastructure projects to establish, upgrade, and improve the GCS packaging,… more
    Merck (12/03/25)
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  • Director Quality Control

    J&J Family of Companies (Raritan, NJ)
    …a member of Johnson & Johnson's Family of Companies, is recruiting for a Director of Quality Control, CAR-T Manufacturing! This position will be located in ... advance the promise of an immunotherapy CAR-T platform and investigational treatment. The Quality Control Director for an Advanced Therapy CAR-T facility leads… more
    J&J Family of Companies (12/19/25)
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  • Senior Director , Site Quality Head,…

    Teva Pharmaceuticals (Parsippany, NJ)
    Senior Director , Site Quality Head, Goa Date: Dec 1, 2025 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job Id: 63901 ... development, standardization, implementation, monitor effectiveness and continuous improvement of Quality Systems, global and local compliance programs, industry… more
    Teva Pharmaceuticals (12/06/25)
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  • Director , Regulatory Affairs CMC

    Taiho Oncology (Princeton, NJ)
    …MAA's, INDs, CTAs, DMFs, ASMFs, etc. and ensures that they conform to current GMP and meet global regulatory requirements. The incumbent may participate in ... Directs and coordinate regulatory activities of external consultants in consultation with Global Executive Director or designee. + Prepare project and/or status… more
    Taiho Oncology (12/09/25)
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  • Associate Director , Inspection Readiness

    Bristol Myers Squibb (New Brunswick, NJ)
    …extensively with teams and leaders across the BMS network. The Associate Director will support BMS' GMP /GDP Inspection Readiness strategy by supporting ... based on a risk-based approach. **Key Responsibilities** * Monitor and assess global regulatory inspection outcomes, enforcement actions, quality and compliance… more
    Bristol Myers Squibb (12/21/25)
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  • Sr. Director of Software Sales - Life…

    Honeywell (Hamilton, NJ)
    …and quality . Operating within a matrixed organization, the Sr Director will collaborate across functions and geographies to deliver customer-centric solutions ... The **Sr Director of Software Sales - Life Sciences** will...process development to commercial scale-up + Demonstrated knowledge of quality systems and regulatory frameworks (eg, GMP ,… more
    Honeywell (11/04/25)
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  • Associate Director , Logistics…

    Merck (Rahway, NJ)
    …execution, along with leadership skills to shape the technical capabilities lead a global , cross-modality technical team. The Associate Director will lead a team ... **Job Description** Reporting into the Director , Logistics and Distribution Technology the Associate Director , Logistics and Distribution Technology will be… more
    Merck (10/16/25)
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  • Director , Commercial Manufacturing…

    Sumitomo Pharma (Trenton, NJ)
    Director , Commercial Manufacturing Validation** . This role functions within SMPA's Global Technology and Quality organization. In this capacity, the ... Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations...are implemented and updated for all development and commercial GMP programs. The individual must have the ability to… more
    Sumitomo Pharma (12/12/25)
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  • Associate Director , Cell Therapy…

    Bristol Myers Squibb (Summit, NJ)
    …partners** + Cell Therapy functions (CT Development, CT Drug Product Operations, CT Quality , VExMO, CTTO, Supply Chain, Finance, Regulatory, etc.) + GPS and Cell ... leadership & collaboration working in, or closely with, Supply Chain, GMP Manufacturing Operations, Manufacturing Science & Technology, Project & Program management,… more
    Bristol Myers Squibb (11/28/25)
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  • Senior Manager, Cell Therapy Manufacturing,…

    Bristol Myers Squibb (Summit, NJ)
    …within the Manufacturing Operations function. This position reports to Associate Director , Manufacturing. **Shift Available:** + Monday - Friday, Onsite Afternoon ... adhere to the BMS values of Inclusion, Accountability, Innovation, Urgency and Passion. GMP : * Is accountable to ensure their Manufacturing Managers and their WCT… more
    Bristol Myers Squibb (12/15/25)
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  • Sr. Manager, Supply Chain

    Mitsubishi Chemical Group (Jersey City, NJ)
    …pharmaceutical company that has tirelessly pursued medical breakthroughs with global reach. Tanabe Pharma Corporation has discovered and produced several ... development, distribution, importation, export, and vendor management in cooperation with Director of Commercial Supply Chain. This incumbent will drive supply chain… more
    Mitsubishi Chemical Group (09/24/25)
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  • Assoc. Dir., Engineering , Combination Products…

    Merck (Rahway, NJ)
    **Job Description** Reporting into the Director Packaging Platform Technical Leadership the Associate Director Medical Device and Combination Product (MDCP) ... supply of commercialized products for the benefit of patients. The Associate Director of MDCP Platform Packaging and Assembly Technical Leadership is integral to… more
    Merck (11/11/25)
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  • Sr. Manager, Microbiology Reliability - Tissue…

    Integra LifeSciences (Princeton, NJ)
    …outcomes and set new standards of care. Under direct supervision of Director , Quality Reliability Microbiology, the Sr. Manager, Microbiology Reliability - ... a medical device manufacturing environment. This position reports into Global Laboratories, Microbiology, and Sterility Assurance but will be...13485, ISO 14644, ISO 14698, BS EN 17141, EU GMP Annex 1, ISO 11135, ISO 11764, ANSI/AAMI ST98,… more
    Integra LifeSciences (11/05/25)
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  • Program Manager

    Catalent Pharma Solutions (Princeton, NJ)
    …that meet or exceed client expectations. The Program Manager will report to the Director , Global Project and Portfolio Management. **Catalent is committed to a ... **Program Manager** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop,… more
    Catalent Pharma Solutions (12/16/25)
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  • Senior Commissioning/Validation Specialist

    Stantec (New York, NY)
    …us create buildings that matter to our world. Together, we are enhancing the quality of life globally through design. Join us and design your place with Stantec. ... FDA or similar facilities where drug products are manufactured, stored in GMP conditions and distributed, including computerized and automated systems which require… more
    Stantec (11/06/25)
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