Chintan Vin
About Chintan Vin
Chintan Vin is the Director (Product Quality Lead) at Bristol Myers Squibb in Seattle, Washington, with extensive experience in quality control within the biotechnology industry and a Bachelor of Science degree in Biotechnology from Washington State University.
Current Role at Bristol Myers Squibb
Chintan Vin holds the position of Director (Product Quality Lead) at Bristol Myers Squibb, stationed in Seattle, Washington. In this significant role since November 2022, he spearheads product quality initiatives, ensuring compliance with regulatory standards. His responsibilities likely involve overseeing quality control processes and leading teams to maintain product integrity, which is crucial in the biotechnology industry.
Previous Roles at Bristol Myers Squibb
Before his current role, Chintan Vin's tenure at Bristol Myers Squibb included several key positions. He was an Associate Director (Product Quality Lead) from 2021 to 2022, a Sr. Principal Scientist (PQL) for six months in 2021, and a Sr. Scientist from 2019 to 2021. In each of these roles, he contributed to maintaining and enhancing product quality, leveraging his extensive experience in quality control.
Work Experience at Immune Design
Chintan Vin worked at Immune Design in various capacities, enriching his expertise in quality control over several years. He served as a QC Manager in 2018, QC Supervisor from 2015 to 2017, Research Associate III from 2013 to 2015, and Research Associate II from 2010 to 2013. These roles, spanning nearly a decade, involved rigorous quality control responsibilities and significant contributions to the company's product development in the biotechnology field.
Educational Background
Chintan Vin graduated from Washington State University with a Bachelor of Science degree in Biotechnology. His academic tenure from 2004 to 2008 encompassed comprehensive studies in Molecular Biology, Microbiology, and Biotechnology. This solid educational foundation provided him with crucial knowledge and skills that underpin his professional expertise in the biotechnology industry.
Expertise in Quality Control and FDA Regulations
Chintan Vin has a robust background in quality control within the biotechnology sector, specifically in areas such as vaccines, oncology, allergy, gene therapy, and infectious disease. His role frequently involves working within U.S. Food and Drug Administration (FDA) regulatory frameworks, ensuring that products meet stringent safety and efficacy standards. His extensive experience makes him adept at navigating complex regulatory environments and implementing rigorous quality control measures.