• Senior Director , MSAT Biologics

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …culture, purification, and formulation + Proven track record in process development , scale-up, and technology transfer of biologics products + Strong ... **Position Overview:** The Senior Director , MSAT Biologics provides strategic and...knowledge of cGMP regulations and ICH guidelines relevant to biologics manufacturing + Experience with PAT ( Process … more
    Otsuka America Pharmaceutical Inc. (10/13/25)
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  • Principal Scientist, Biologics Analytical…

    Merck (Rahway, NJ)
    …stability assays for testing of clinical trial material and in support of product and process development + A strong team player with excellent oral and written ... **Job Description** The Biologics Analytical Research & Development department...and Capillary Electrophoresis (CE) techniques + Extensive experience with process - and impurity-related residual assay development using… more
    Merck (08/19/25)
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  • Senior Director , Early Development…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …drug development process , preferably with experience in early phase development covering both biologics and small molecule - Experience in managing and ... **Senior Director , Early Development Team Lead** **Role...- Working knowledge of all functional areas of exploratory development , including, CMC (small molecules and biologics ),… more
    Otsuka America Pharmaceutical Inc. (10/17/25)
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  • Senior Clinical Director , Oncology Early…

    Merck (Rahway, NJ)
    …marketed Oncology medicines. Our Oncology medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the ... in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and Assist the Executive Director /AVP in… more
    Merck (10/25/25)
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  • Associate Director , MSAT, Downstream Drug…

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …relevant experience in the biopharmaceutical industry with a strong focus on biologics downstream process development , scale-up, technology transfer, and/or ... **Job Summary** **​** The Associate Director , MSAT - Downstream provides specialized technical leadership...Collaborate closely with Upstream MSAT, Validation MSAT, QA, Regulatory, Process Development , Analytical Development , and… more
    Otsuka America Pharmaceutical Inc. (10/17/25)
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  • Director , Business Development…

    Boehringer Ingelheim (NJ)
    **Description** In the role of Director of Business Development & Key Account Management (BD&KAM) you will primarily execute on the contract manufacturing ... an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our… more
    Boehringer Ingelheim (10/16/25)
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  • Director , Raw Materials & Medical Device…

    Merck (Rahway, NJ)
    **Job Description** **Raw Materials & Medical Device Director , Small Molecule Analytical Research & Development ** The Small Molecule Analytical Research and ... during internal and external compliance audits + Ensuring operational excellence and drive process improvements + Staff development and talent recruiting + Work… more
    Merck (10/15/25)
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  • Director , Microbiology GMP Operations AR&D

    Merck (Rahway, NJ)
    …Our Research and Development Division's microbiology team is seeking a Director for the Rahway NJ GMP microbiology operations. The primary objective of the ... formulations, and their processes for non-sterile and sterile products. The Director will also collaborate with Development Quality, Pharmaceutical Operations,… more
    Merck (10/29/25)
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  • Executive Director Quality Systems…

    Bristol Myers Squibb (Madison, NJ)
    …strategic compliance initiatives in partnership with cross-functional teams, including Process Development , Analytical Development , Global Manufacturing ... lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Executive Director , Cell Therapy Quality Compliance, is responsible for ensuring robust… more
    Bristol Myers Squibb (10/22/25)
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  • Senior Director , Cell Therapy Quality…

    Bristol Myers Squibb (Madison, NJ)
    …qualification, validation, and routine operation. + Partner closely with Automation, Engineering, Process Development , Regulatory, Supply Chain, and CMC teams to ... digitized quality platforms. + Proven ability to lead quality support for process development , MS&T, and external manufacturing initiatives. + Strategic thinker… more
    Bristol Myers Squibb (10/30/25)
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