
A leading pharmaceutical firm in San Francisco is seeking an experienced professional to define and execute CMC strategies for oral peptide drug products. Candidates should possess a Ph.D. or M.S. in Pharmaceutical Sciences and have over 15 years of experience in pharmaceutical development, particularly with oral solid dosage forms. This role emphasizes leadership, collaboration with cross-functional teams, and the ability to manage CDMO relationships. Strong expertise in CMC documentation and regulatory submissions is crucial.
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