Joe Zhou is an accomplished regulatory affairs and analytical development professional with extensive experience in the pharmaceutical industry. Currently serving as the Senior Director of Regulatory Affairs - CMC at EyePoint Pharmaceuticals, Joe has previously held key positions including Director of Analytical Development at Entasis Therapeutics and Astria Therapeutics, Inc., as well as Head of Pharmaceutical Development and Regulatory CMC at CutisPharma Inc. Additionally, Joe served as Associate Director of Analytical Development at Merck, demonstrating a strong track record in driving development initiatives and ensuring compliance in complex regulatory environments.
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