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Mayo Brown is an experienced professional in the field of regulatory science and quality assurance, currently serving as Associate Director of Regulatory Science - CMC at Oxford Biomedica since March 2022. Responsibilities include developing global regulatory CMC strategies, leading high-quality regulatory submissions for gene therapy products, and assessing changes for post-approval modifications. Previously, Mayo held the role of Sr. Manager of Regulatory Science - CMC at Homology Medicines, where oversight of external manufacturing and quality operations was a key focus. Additional experience includes positions as Manufacturing Specialist at bluebird bio and Sanofi Genzyme, contributing to various aspects of manufacturing operations, technology transfer, and compliance. Educationally, Mayo holds a Bachelor's degree in Chemical Engineering from Villanova University.