Latest Pharmaceutical Product Development jobs in Bernardsville, NJ

40 Pharmaceutical Product Development Jobs in Bernardsville, NJ

Manager, U.S. Oncology Product Communications Daiichi Sankyo, Inc. - Bernards, NJ Education Qualifications (from an accredited college or university) - Bachelor's Degree in relevant discipline required \r\n Experience Qualifications - 4 or More Years Experience in a corporate, product 3 days ago
Senior Manager Regulatory Affairs Gan & Lee Pharmaceuticals - Bridgewater, NJ, United States in a scientific or related discipline, 5+ years of pharmaceutical industrial experience, at least 3 years of regulatory CMC experience with US product development. • Deep knowledge of US and EU regulations 13 days ago
Senior Regulatory Affairs Associate Breckenridge Pharmaceutical, Inc. - Berkeley Heights, NJ, United States or product development operations. Familiar with cGMP/cGCP requirements. Required to attend off-hours teleconferences with overseas partners. 14 days ago
Director, R&D Quality, Global RD/PV QA Daiichi Sankyo, Inc. - Bernards, NJ in the area of Clinical Development Must possess a profound understanding of the science of product development Demonstrated accomplishments working within a global/matrix environment in the pharmaceutical 2 days ago
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Senior Quality Assurance Specialist Germer International - Pharmaceutical Recruiting - Piscataway, NJ, United States in real-time to maintain manufacturing efficiency and product quality. Qualifications: Bachelor's degree Experience in formulation development within the pharmaceutical industry, with a strong understanding 7 days ago
Stability Scientist LanceSoft, Inc. - New Brunswick, NJ, United States Substance and Drug Product manufacturing and good understanding of analytical and/or Microbiology methods. Very good skills to drive development of technical or scientific initiatives for solving complex 10 days ago
Director, Regulatory Affairs Companion Diagnostics Daiichi Sankyo, Inc. - Bernards, NJ of our oncology pharmaceutical products. Provides innovative approaches to resolve complex regulatory issues and increase speed to patients. Responsibilities CDx development: Provide critical strategic and tactical 6 days ago
Associate Director, Tech Management Lead mAb Daiichi Sankyo, Inc. - Bernards, NJ Extensive experience in CMC related functions including (mAb, Drug Substance, Drug Product, or New Modality) process and product development preferred Travel Ability to travel up to 30%. Global and domestic 14 days ago
Stability Scientist Eclaro - New Brunswick, NJ, United States and guidance documents. A thorough knowledge of cGMP regulations as referenced in The Code of Federal Regulations (21CFR) and their specific application to stability programs in a pharmaceutical manufacturing 29 days ago
Senior Statistical Analyst (Remote) - Pipeline Abbvie - Madison, NJ of new pharmaceutical products. The primary responsibilities for this role include the analysis and reporting of clinical trial data and leading the statistical programming activities for clinical studies 4 days ago

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