Carolyn Glickman is an experienced professional in the fields of quality assurance and regulatory affairs, currently serving as the Premarket Quality Chapter Lead for Clinical Collaboration at Roche. Previously, Glickman held the position of Director of Regulatory Affairs at Visby Medical and served as Director of Quality and Regulatory at Complete Genomics Inc. Glickman's earlier roles include Senior Manager of Quality Engineering at Genomic Health and Senior QA Specialist at Baxter BioScience, where Glickman also worked as a Principal Engineer. Glickman holds a Bachelor of Science in Biomedical Engineering from The Johns Hopkins University and a Master of Science in Chemical Engineering from UCLA.
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