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Regulatory Affairs Associate jobs - Bridgewater, NJ

Viewing 1 - 7 of 8 jobs

  • Regulatory Affairs Associate III

    Ascent Services Group - Elizabeth, NJ

    Regulatory Affairs Associate III Elizabeth, NJ RESPONSIBILITIES Regulatory Submissions Preparation of ANDAs, ... as Pharmacy, Chemistry, Biology, etc. 2 years in Regulatory Affairs in generic Pharmaceutical Industry, or 2-4 years...

    22 hours ago from Ascent

  • Regulatory Affairs Labeling Specialist

    Novo Nordisk - Princeton, NJ

    Requisition ID 34616BR Title Regulatory Affairs Labeling Specialist Job Category Regulatory Affairs Job Description ... CMR, Legal, Supply Chain and counterparts in NNAS Regulatory Affairs. Has a positive approach to work projects...

    16 hours ago from NOVO Nordisk

  • Regulatory CMC Technical Associate

    Advanced Clinical - Bridgewater, NJ

    Job Number: 433903 Regulatory CMC Technical Associate OVERVIEW Author Module 3 submission documentation according to ... project teams. The Regulatory CMC Technical Associate may be called upon to author technical reports.

    23 hours ago from

  • Physician (Associate Chief of Staff Education)

    U.S. Department of Veterans Affairs - East Orange, NJ

    with demonstrated leadership ability to serve as the Associate Chief of Staff for Education (ACOS/E). The ACOS/E ... training requirements. Educates VANJHCS leadership about regulatory and accreditation standards as they pertain to...

    22 hours ago from U.S. Department of Veterans Affairs

  • Associate Director/ Director, Clinical Quality Management

    Lexicon Pharmaceuticals - Basking Ridge, NJ

    Job Description: Lexicon Pharmaceuticals is currently recruiting for an Associate Director/Director of Clinical Quality ... Job Summary: The Associate Director/Director of Clinical Quality Management will lead the development and implementation...

    20 hours ago from Regulatory Affairs Professionals Society

  • Associate Clinical Research Scientist

    Novartis - East Hanover, NJ

    Development) as well as Investigator Initiated(Medical Affairs) studies Skills Languages: Fluent English (oral and ... and with an external audience. 9. Project management experience desired 10. Knowledge of GCP and regulatory...

    18 hours ago from

  • Medical Director - Clinical Trials - Inhalable Therapeutics

    Dmc - Summit, NJ

    activities. *** Create and edit clinical sections of regulatory documents including IND applications or NDAs, ... Development Clinical Studies Clinical Trials Medical Affairs Lead Associate Medical Director Lung Infection...

    22 hours ago from