• Associate Director, Regulatory Affairs

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    **Job Description Summary** As Associate Director, Regulatory Affairs, you will be responsible for leading RA team members involved in device project activities and ... Thursday. Associates may work at home on Friday. **Job Description ** We are **the makers of possible** BD is...of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products… more
    BD (Becton, Dickinson and Company) (08/27/25)
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  • Director, Regulatory Policy & Intelligence

    Organon & Co. (Jersey City, NJ)
    **Job Description ** **The Position** Leading the Regulatory Policy and Intelligence activities for Global Regulatory Affairs covering all Therapeutic Areas and ... division, R&D departments as well as commercial organization and manufacturing organizations. + Leveraging new technologies where possible, drive innovative… more
    Organon & Co. (07/23/25)
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  • Compliance Investigator

    Actalent (Allendale, NJ)
    …writing and reviewing deviations and investigations. + Experience working within a pharmaceutical company supporting manufacturing . + Experience within a quality ... Job Title: Compliance Investigator Job Description We are seeking a dedicated Investigator responsible...and complete investigations and deviations to ensure compliance with manufacturing and GMP standards. + Conduct root cause analysis… more
    Actalent (09/03/25)
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  • Foundations for the Future Rotational Development…

    Syensqo (West Deptford, NJ)
    …a relative environment. This may include but is not limited to - Specialty Chemical, Pharmaceutical Manufacturing , Oil & Gas, Pulp & Paper, or Food & Beverage ... one in hands-on field work and advanced analytical problem-solving in chemical manufacturing environments around the country. The Program is designed to offer you… more
    Syensqo (08/15/25)
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  • Principal Scientist (Director) - Outcomes Research…

    Merck (Rahway, NJ)
    **Job Description ** This position resides within our company's Value and Implementation (V&I), Outcomes Research organization, which is responsible for real-world ... a relevant discipline (eg, Outcomes Research, Health Economics, Epidemiology, Pharmaceutical Administration, Public Health, Health Policy, Medicine, or Clinical… more
    Merck (09/03/25)
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  • Associate Director, Small Molecule Analytical…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …analysis techniques, fostering their professional growth and expertise in pharmaceutical stability studies. + Collaborate cross-functionally with analytical team ... in a GMP environment. + Prior experience overseeing and working with external manufacturing and analytical sites + Expertise in chromatographic (HPLC, UPLC, GC) and… more
    Otsuka America Pharmaceutical Inc. (08/27/25)
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  • US Executive Director, Medical Affairs,…

    Merck (Trenton, NJ)
    **Job Description ** The Executive Director (ED) for US Medical Affairs (USMA) understands Our Company's enterprise level strategies and leads cross-functionally with ... programs + 5 years of front-line field medical leadership in the pharmaceutical industry, with teams having responsibility for scientific exchange and research… more
    Merck (08/20/25)
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  • Associate Director External Quality Assurance

    Organon & Co. (Jersey City, NJ)
    **Job Description ** **The Position** Individual contributor responsible for ensuring that all Organon products managed by External Quality Assurance (EQA) are ... launches, historical relationship between Organon and the contract manufacturer, manufacturing process complexity. The incumbent ensures that effective and robust… more
    Organon & Co. (08/19/25)
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  • Sr MES PAS-X Specialist role

    Capgemini (Raritan, NJ)
    **Job description ** **:** Support autologous manufacturing Site. This is a manufacturing support role responsible for the generation of electronic ... teams. **KEY RESPONSIBILITIES** **:** Job Scope And Responsibilities Requirements: Manufacturing Electronic Batch Record (EBR) generation using PAS-X () Hands-on… more
    Capgemini (07/26/25)
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  • Senior Analyst, QC Biochemistry

    BeOne Medicines (Pennington, NJ)
    **General Description :** Perform QC Biochemistry laboratory activities to support GMP manufacturing , testing and release of material, intermediates and finished ... ensure timely generation and reporting of test results in support of manufacturing operations. + Support routine operations, including but not limited to instrument… more
    BeOne Medicines (08/29/25)
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