Latest Pharmaceutical Regulatory Affairs jobs in Florham Park, NJ

26 Pharmaceutical Regulatory Affairs Jobs in Florham Park, NJ

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 23 days ago
Senior Manager, US Regulatory Affairs - GDP Shionogi Inc. - Florham Park, New Jersey in a scientific discipline such as life sciences, pharmacy, bioscience; advanced degree preferred. 5+ years of experience in regulatory affairs within the pharmaceutical or biotech industry, with a focus on quality 23 days ago
Associate Director, US Regulatory Affairs, Advertising & Promotion Proclinical Staffing - Morristown, 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 18 days ago
Senior Director, Regulatory Affairs - GDP Shionogi Inc. - Florham Park, New Jersey Qualifications Bachelor's degree in a scientific discipline such as life sciences, pharmacy, bioscience; advanced degree preferred. 12+ years of experience in regulatory affairs within the pharmaceutical 23 days ago
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Regulatory Manager Mindlance - Bridgewater, NJ, United States of relevant Regulatory Affairs experience (regionally and/or global), in early development. Yesterday
Regulatory Affairs Specialist Katalyst Healthcares & Life Sciences - Short Hills, New Jersey preferred). Bachelor's or master's degree required in science, engineering or related field (advanced degree preferred). Proven and relevant regulatory affairs experience in pharmaceutical, vaccine 9 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 16 days ago
Senior Scientist/Associate Director RACMC Daiichi Sankyo, Inc. - Bernards, NJ minutes. - Works with cross functional teams and various departments to include Marketing, Medical Affairs, Regulatory Affairs, Supply Chain Technical Operations, Pharmaceutical Technology and others where 12 days ago
USA-Regulatory Affairs Specialist Project Lead I (Scientific) The Fountain Group LLC - Bridgewater, New Jersey and strategy in collaboration with GRT (Global Regulatory Team) and is accountable for the communication of the key outcomes to senior management. Experience: • At least 8-10 years of relevant pharmaceutical Yesterday
USA-Regulatory Affairs Specialist Project Lead I (Scientific) Mindlance - Bridgewater, New Jersey years of relevant pharmaceutical/biotechnology experience in R&D, including at least 5 years of relevant Regulatory Affairs experience (regionally and/or global). EEO: “Mindlance is an Equal Opportunity 3 days ago

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