Associate Director, Regulatory Affairs – CMC Small Molecules
Monte Rosa Therapeutics
100-1000 employeesJob Description
Department: Not specified
Skills & Keywords
Small Molecules, Regulatory Affairs, CMC, Biotechnology, CMOS, Regulatory Requirements, GCP, NDA, FDA, Document Review, Scientific Writing, Pharmaceutical Industry, IND, Project Management, eCTD, Chemistry, cGMP, Pharmaceutical Sciences
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