Virginia Carroll

Dr. Carroll is a Senior Pharmaceutical Quality Assessor within the Division of Biotechnology Manufacturing, Office of Pharmaceutical Manufacturing Assessment, OPQ, CDER, FDA and serves as a team lead for microbiology review of biologic license applications and supplements, including biosimilars. She has participated on multiple pre-license inspections for protein biological products with a focus on aseptic processing and sterility assurance. Prior to joining FDA in 2017, she completed post-doctoral studies at the University of Maryland, Baltimore and taught college microbiology courses. She holds a PhD in in Microbiology from the University of Virginia.