Carrie Brewer is an experienced scientist in vaccine development with a strong background in Good Manufacturing Practice (GMP) laboratory operations. Carrie worked at Pfizer (formerly Wyeth) as a Scientist II from January 2007 to November 2010, where responsibilities included maintaining regulatory compliance and managing project timelines. Prior to that, Carrie held positions at Wyeth and Catalent Pharma Solutions, with responsibilities ranging from GMP stability testing to conducting investigations of discrepancies in data. Carrie began the career as a Scientist I at Kelly Scientific Resources, supporting GMP release testing. Earlier experience includes a position as a Health Information Systems Technician II at North Oaks Medical Center, where tasks involved patient documentation and medical record management. Carrie holds a Bachelor of Science in Microbiology from Southeastern Louisiana University.
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