Regulatory jobs in New Brunswick

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Found 8 jobs

  • Lead, GxP External Engagement

    • New Brunswick, NJ
    • Bristol-Myers Squibb Company

    Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on he

  • PDT ANALYTICAL RESEARCH/25

    • New Brunswick, NJ, United States
    • Bristol-Myers Squibb Company

    Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on he

  • Research Investigator II

    • New Brunswick, NJ, United States
    • Bristol-Myers Squibb Company

    Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on he

  • Research Investigator

    • New Brunswick, NJ, United States
    • Bristol-Myers Squibb Company

    Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on he

  • Regulatory (CMC) Compliance Manager

    • New Brunswick, NJ, United States
    • Bristol-Myers Squibb Company

    Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on he

  • Senior Research Investigator

    • New Brunswick, NJ, United States
    • Bristol-Myers Squibb Company

    As the Sr. Research Investigator you will be responsible for route scouting and the design and implementation of safe, efficient and robust chemical p

  • Research Investigator II

    • New Brunswick, NJ, United States
    • Bristol-Myers Squibb Company

    Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on he

  • Senior CMC Documentation Scientist

    • New Brunswick, NJ, United States
    • Bristol-Myers Squibb Company

    This position involves coordinating filing activities, compiling information from scientists, and authoring the CMC sections of regulatory documents (