Latest Cmc Regulatory Affairs jobs in Lexington, MA

19 Cmc Regulatory Affairs Jobs in Lexington, MA

Associate Director, Regulatory Affairs CMC Accede Solutions Inc - Lexington, Massachusetts Hybrid Role The Associate Director of Regulatory Affairs CMC will support development CMC team activities for an emerging portfolio of biologics products. This position will oversee CMC Health 21 days ago
Associate Director, Regulatory Affairs CMC Keros Therapeutics - Lexington, MA Applicants and employees are considered for positions and are evaluated without regard to mental or physical disability, race, color... 29 days ago
Senior Medical Director Novo Nordisk - Lexington, MA , , Medical Writing, Program Management, CMC and Regulatory Affairs teams. Will be interfacing with both internal TRU and Novo Nordisk global development leadership, and external stakeholders including KOLs 2 days ago
Director, Regulatory Affairs Vaccines CMC Takeda - Boston, MA, United States Vaccines CMC where you will provide program leadership and develop CMC regulatory strategy for global vaccine programs in various stages of development. You will represent the vaccine regulatory affairs team 9 days ago
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Medical Director Novo Nordisk - Lexington, MA with the VP Medical/Scientific Development, Clinical Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams. Will be interfacing with both internal and external 6 days ago
Director, Non-Clinical Toxicology MapLight Therapeutics, Inc. - Burlington, MA, United States Collaborate with CMC, Program & Portfolio Management, Clinical, and Regulatory Affairs to develop program-specific strategies for appropriate data generation in support of development candidate nomination, IND 6 days ago
Senior Director, CMC HireMinds - Watertown, MA, United States and CMC teams and related functions, including discovery, non-clinical development, Formulation, Analytical Development, QA, and CMC Regulatory Affairs. Formal descriptions can be supplied for interested 12 days ago
Project Manager, CMC Regulatory Affairs GSK - Waltham, MA together. The Project Manager, CMC Regulatory Affairs will be responsible for the CMC regulatory activities in the investigational, late phase development and/or early commercial lifecycle management of GSK Yesterday
Senior Director, Program Leader Astria Therapeutics, Inc. - Boston, MA, United States and integrate diverse R&D activities including but not limited to, preclinical research, clinical development, CMC, regulatory affairs, new product planning, business development and finance. The ideal candidate 6 days ago
Director, GRA CMC Pharmaceuticals, Oligonucleotides Takeda - Cambridge, MA, United States to the Executive Director and Head, CMC Regulatory Affairs, Pharmaceuticals. How you will contribute: Responsible for demonstrating Takeda leadership behaviors. Serve as a member of the GRA-CMC Pharmaceuticals 12 days ago

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