Edgar S. is an experienced professional in quality engineering and validation within the biotechnology and pharmaceutical industries. With a background that includes roles at Abbott as a Quality Engineer II, Takeda, Thermo Fisher Scientific, Gilead Sciences, and Grifols, Edgar has expertise in new product development, change proposal approvals, process validations, and quality control within regulated environments. Notably, responsibilities have included leading manufacturing teams, overseeing validation protocols, and advising on process optimizations for medical device manufacturing. Edgar holds a Master of Science in Quality Assurance from California State University-Dominguez Hills and a Bachelor of Science in Biology from Loyola Marymount University.
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