Latest Pharmaceutical Regulatory Affairs jobs in Bridgewater, NJ

23 Pharmaceutical Regulatory Affairs Jobs in Bridgewater, NJ

Associate Director, US Regulatory Affairs, Advertising & Promotion Proclinical Staffing - Plainsboro, NJ, United States Associate Director, US Regulatory Affairs, Advertising & Promotion - Permanent - NJ & MA Proclinical is seeking an Associate Director, US Regulatory Affairs, Advertising & Promotion for a large 5 days ago
GPV Case Management Product Specialist GForce Life Sciences - Princeton, NJ, United States experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions **Relevant experience includes experience in the pharmaceutical 2 days ago
Senior Director, Global Regulatory Leader, CAR-T Therapy Johnson and Johnson - Raritan, NJ years in drug development any of the following areas (e.g. Global Regulatory Affairs, R&D or health authority role) is required. * 10 years within the pharmaceutical/biotech industry is required, along 2 days ago
GPV Submission Specialist GForce Life Sciences - Princeton, NJ, United States experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions **Relevant experience includes experience in the pharmaceutical 22 days ago
Forum: Start a Discussion Join
Manager Global CMC Regulatory Affairs Johnson and Johnson - Raritan, NJ Affairs * Conducts due diligence/licensing evaluations where needed * Bachelors in Science (engineering, biological, pharmaceutical or chemical) with minimal 6 years of proven experience or equivalent 7 days ago
Associate Director, Regulatory Affairs Catalent - Somerset, New Jersey Associate Director, Regulatory Affairs Position Summary: Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing 3 days ago
CMC - Regulatory Affairs Katalyst Healthcares & Life Sciences - South Plainfield, New Jersey and relevant regulatory affairs experience in pharmaceutical, vaccine, or biological products; or related fields Knowledge and hands on experience on Animal Health CMC Marketing authorization experience. Proven 7 days ago
Scientific Director, Medical Affairs- CNS/Psychiatry Florham Park, NJ with regulatory. activities. Qualifications Advanced Degree PhD or PharmD. Additional post doctorate experience highly preferred. Typically, 5-105 years of experience in the pharmaceutical industry or equivalent 17 days ago
Quality - Trial Supplies Manager Trial Supplies Manager Artech LLC - Summit, New Jersey Management, Client Affiliates, Medical Affairs (MA), Regulatory, CMC, QA, Packaging Vendors, CRO s, IRT Organizations, and Global Clinical Supply Chain Functional Operations to ensure all needs are met 3 days ago
Associate Director/Director, Regulatory Affairs - GDP Shionogi Inc. - Florham Park, New Jersey in a scientific discipline such as life sciences, pharmacy, bioscience; advanced degree preferred. 7+ years of experience in regulatory affairs within the pharmaceutical or biotech industry, with a focus on quality 10 days ago

Top locations