Jyothy Pillai | VP, Head of Regulatory Affairs & Quality Assurance
Ocugen

Jyothy has over 20 years’ experience in Biopharmaceutical Research, Quality Assurance and Regulatory Affairs at GlaxoSmithKline and Merck. During her career, she has contributed to the development and global commercialization of early, mid and late phase Biologics including recombinant proteins, monoclonal antibodies, antibody drug conjugates, bispecific & fusion proteins. Jyothy is a trained auditor, led and participated in several GMP audits, hosted regulatory inspections, and led implementation of GMP facilities & audit ready processes. Prior to joining Ocugen, Jyothy was part of the late phase biologics development team of Global Regulatory affairs at Merck, responsible for global regulatory clinical trial applications for co-formulated Biologics in 40 markets including US, Canada, China & European Union. Jyothy obtained her MS in Chemistry from Dayalbagh University, Agra, India and M.S. in Regulatory Affairs and Quality Assurance from Temple University School of Pharmacy, Philadelphia, PA.