Ying Zheng is a seasoned professional in regulatory affairs with extensive experience in the pharmaceutical industry. Currently serving as Senior Manager in Regulatory Affairs at Sanofi since August 2017, Ying Zheng focuses on US regulatory strategies for rare diseases, highlighting expertise in expedited programs and FDA interactions. Prior experience includes managerial roles at Teva Pharmaceuticals and a regulatory affairs position at AustarPharma, with responsibilities encompassing ANDA submissions and project coordination. Ying Zheng also has a strong academic background, holding a Ph.D. in Microbiology and Immunology from Stony Brook University, alongside an M.Phil. from The University of Hong Kong and a B.S. from Peking University.
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