Penny Davis is a Technical Regulatory Senior Director at Genentech, where they leverage over 17 years of experience in managing diverse biotherapeutic modalities throughout the product lifecycle. Previously, Penny held roles at notable organizations including Pfizer, Biogen Inc, and MedImmune, contributing to regulatory affairs and global CMC strategies. Prior to these positions, Penny completed a PhD in Pharmacology at the University of Alabama at Birmingham and served as a Howard Hughes Post-doctoral fellow in Internal Medicine at Washington University in St. Louis.
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