Latest Cmc Regulatory Affairs jobs in Kenilworth, NJ

21 Cmc Regulatory Affairs Jobs in Kenilworth, NJ

Principal Scientist (R5), Biologics Analytical Research & Development (B-AR&D) Merck - Kenilworth, NJ GMP laboratories, Biologics Process Research and Development, Global Quality and Regulatory Affairs-CMC, and our partners in in the commercial/manufacturing to support commercialization of our company's 23 days ago
Trial Supplies Manager Ivory Systems - Summit, NJ, United States and Service Providers, including but not limited to Clinical Research and Development, Global Study Management and Monitoring (GSMM), Project Management, BMS Affiliates, Medical Affairs (MA), Regulatory, CMC Yesterday
Trial Supplies Manager Innova Solutions - Summit, NJ, United States Affairs (MA), Regulatory, CMC, QA, Packaging Vendors, CRO's, IRT Organizations, and Global Clinical Supply Chain Functional Operations to ensure all needs are met. Working with teams for optimal use Yesterday
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
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Manager Global CMC Regulatory Affairs Johnson and Johnson - Raritan, NJ Johnson & Johnson Innovative Medicine is recruiting for a Manager, CMC Regulatory Affairs to be located in Raritan, NJ; Titusville, NJ; or Beerse, Belgium. At Johnson & Johnson,we believe health 7 days ago
CMC2 - Regulatory Affairs - Animal Health Diverse Lynx - Rahway, New Jersey Role: CMC2 - Regulatory Affairs - Animal Health Type: Contract Contract Location: Rahway, NJ - Onsite from day 1 (locals only) Contract Duration: 11 months Hourly Pay Rate: $44 W2 and $52 C2C 22 days ago
Scientific - Global Regulatory CMC Manager TechDigital Corporation - Summit, New Jersey . 5. Represent Regulatory CMC on cross-functional development/commercial teams and Regulatory Affairs teams. 6. Participate in global regulatory interactions with health authorities, with supervision. 7 Yesterday
Executive Director, Biologics Analytical Research and Development GMP Operations Lead Merck - Rahway, NJ 07065 with staff, colleagues across CMC development and commercialization, Quality Assurance, Technical Operations, and CMC Regulatory Affairs as needed to ensure understanding of needs, proper prioritization 6 days ago
Trial Supplies Manager LanceSoft Inc - Summit, New Jersey , Global Study Management and Monitoring (GSMM), Project Management, Clients Affiliates, Medical Affairs (MA), Regulatory, CMC, QA, Packaging Vendors, CRO s, IRT Organizations, and Global Clinical Supply 2 days ago
Quality - Trial Supplies Manager HonorVet Technologies - Summit, New Jersey , 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. " Working with teams for optimal 3 days ago

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