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Suresh Guntireddygari PhD has several years of experience in the field of Quality Assurance and Regulatory Compliance. Suresh started their career in 2006 as a Postdoctoral Research Associate at Organix Inc. Suresh then worked at Inotek Pharmaceuticals as a Scientist in Medicinal Chemistry from 2007 until 2007. After that, they worked for over a decade at PerkinElmer, Inc. in various roles including Principal Quality Assurance and Regulatory, Principal GMP Scientist, and Staff Scientist. In 2019, they joined Lyra Therapeutics as Principal Quality Assurance, and in 2020 they moved to Enanta Pharmaceuticals as Manager, Quality Assurance, CMC/Development, where they worked until mid-2022. Suresh then joined Vedanta Biosciences, Inc. as Associate Director, Quality Assurance until early 2023, when they joined Bill & Melinda Gates Medical Research Institute as QA GMP Compliance Lead.

Suresh Guntireddygari PhD received their Ph.D. from Indian Institute of Chemical Technology, focused on Synthetic Organic & Medicinal Chemistry. Suresh received their M.S. from Osmania University, specializing in Organic Chemistry. Following their Ph.D., they worked as a Postdoctoral Research Associate in Medicinal Chemistry at the University of South Florida.