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Mayo Brown

Sr Manager Regulatory And Product Quality at Oxford Biomedica Solutions

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.

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