Marilyn Monroy is a Principal Scientist (Director) in Global Regulatory Affairs & Clinical Safety, Vaccines CMC at Merck & Co. They have previously served as a Senior Regulatory Associate at GSK, participating in the submission and approval of global CMC applications, and held various engineering roles at Merck from 2008 to 2012, including Staff Biochemical Engineer. With a Master of Science in Quality Assurance Regulatory Affairs from Temple University, they also hold multiple degrees in Chemical Engineering from the University of Florida. Marilyn has a strong background in both regulatory affairs and biochemical engineering, contributing significantly to the development and transfer of live virus vaccines.
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