Bryan Vincent
About Bryan Vincent
Bryan Vincent is the Upstream Processing Supervisor at Bristol-Myers Squibb in Hopewell, with 18 years of experience in cGMP manufacturing and a background in biology from Rutgers University.
Title
Bryan Vincent holds the title of Upstream Processing Supervisor at Bristol-Myers Squibb. He also serves as a Senior Manufacturing Associate at the same company, located in Hopewell.
Current Role at Bristol-Myers Squibb
Bryan Vincent started his current role as Upstream Processing Supervisor at Bristol-Myers Squibb on March 1, 2018. He oversees upstream processing activities and ensures adherence to current Good Manufacturing Practices (cGMP). In addition to this role, he also holds the position of Senior Manufacturing Associate, contributing his extensive expertise to multiple facets of the company's operations.
Previous Experience
Bryan Vincent has a diverse background in biopharmaceutical production. He worked at Medarex as an Assistant Manager, Biopharm Production for 10 years (2001-2011) and as an Assistant/Associate Scientist for 4 years (2001-2005). He also served as a Supervisor at Biopharmaceutical Production from 2005 to 2007.
Education and Expertise
Bryan Vincent earned a Bachelor of Science in Biology from Rutgers University. With 18 years of experience in cGMP manufacturing, he specializes in areas such as High-Performance Liquid Chromatography (HPLC), inventory management, process engineering, protocols, supervisory skills, training, and validation.
Years of Experience in cGMP Manufacturing
Bryan Vincent brings 18 years of experience in cGMP manufacturing to his current roles at Bristol-Myers Squibb. His expertise spans various specialized fields, including HPLC, process engineering, and supervisory skills, making him a valuable asset in both his supervisory and manufacturing associate capacities.