• Associate Principal Scientist, Regulatory Affairs…

    Organon & Co. (Jersey City, NJ)
    Director ) is responsible for developing and implementing Regulatory Chemistry , Manufacturing & Controls (CMC) strategies for assigned small molecule and/or ... lead the preparation and submission of CMC dossiers for programs in clinical development, marketing applications and post-approval life cycle maintenance phases. The… more
    Organon & Co. (07/22/25)
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  • Senior Specialist, Project Management…

    Merck (Rahway, NJ)
    …for building and executing CMC development plans. Under the guidance of the CIPM Director & Portfolio Lead, the core responsibility of this individual will be to ... lead project management efforts to support Chemistry Manufacturing & Controls (CMC) product development from First in Human to Transfer to Supply, driving line of… more
    Merck (08/28/25)
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  • Lab Supervisor- Chemistry

    Hunterdon Health Care System (Flemington, NJ)
    …other hospital support staff. Reporting Relationships Reports to (position): Director Laboratory Services Supervises (position(s): Medical Laboratory Scientists, ... Assistants Qualifications Minimum Education: Required: Bachelor's Degree in chemical, biological, clinical laboratory science or medical technology from an… more
    Hunterdon Health Care System (08/09/25)
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  • Director , Clinical Microbiology

    Atlantic Health System (Morristown, NJ)
    …CAP and industry best practice system-wide Director of Quality, and the Medical Director under the supervision of the VP, Laboratory Services. All activities ... The Technical Director supports the Clinical disciplines of... Clinical disciplines of the laboratory such as Chemistry , Hematology, Microbiology, Specialty Testing, and Blood Bank to… more
    Atlantic Health System (08/22/25)
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  • Sr. Director , Scientific & Medical

    Taiho Oncology (Princeton, NJ)
    …vision allow us to consistently pursue and develop life-changing innovations. As Senior Director of Scientific & Medical Communications, you'll play a pivotal ... at every stage of the product lifecycle. Position Summary: ​​ The Sr. Director , Scientific & Medical Communications (SDSMC) leads the strategic development,… more
    Taiho Oncology (08/09/25)
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  • Director , Small Molecule Formulation…

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    Director , Formulation Development is an experienced leader in the development of pharmaceutical products in a virtual environment with extensive technical, strategic ... to work effectively with CDMOs. The position reports to Executive Director , CMC & Product Development. **Job Description** **Pharmaceutical Development:** + You… more
    Otsuka America Pharmaceutical Inc. (09/05/25)
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  • Associate Director , Small Molecule…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    **Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and drug ... studies. + Collaborate cross-functionally with analytical team members, process chemistry , formulation development, regulatory affairs, quality assurance, and other… more
    Otsuka America Pharmaceutical Inc. (08/27/25)
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  • Senior Director , Global Product Quality,…

    Bristol Myers Squibb (Summit, NJ)
    …their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Senior Director , Cell Therapy Global Product Quality Lead ( Sr. Dir. CT- ... , control strategies, comparability, specifications, and stability . The Sr. Director m onitors commercial operations through periodic reviews of process and… more
    Bristol Myers Squibb (09/05/25)
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  • Director Regulatory Affairs

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …+ Bachelor's degree or advanced degree in technical area such as biology, chemistry , engineering or medical -related field and a minimum of nine years ... **maker of possible** with us. The Regulatory Affairs (RA) Director is responsible for the management and setting the...Advance degree preferred. + RAC certification. + Experience with Clinical Trial applications (US IDE). + Medical more
    BD (Becton, Dickinson and Company) (08/08/25)
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  • Associate Director , Literature Analyst

    Merck (Rahway, NJ)
    …through information science. We are seeking a passionate, experienced Associate Director to connect scientists and stakeholders with focused scientific literature ... knowledge services that empower research teams across the organization. As Associate Director , you will collaborate closely with cross-functional teams to design and… more
    Merck (09/06/25)
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