Steve Ryan

Steve Ryan is an experienced regulatory operations professional with a career spanning over two decades in the biopharmaceutical industry. Currently serving as Senior Director of Regulatory Operations at Zenas BioPharma since March 2024, Steve has a strong history of managing regulatory submissions and systems across various organizations. Previous roles include Director of Regulatory Operations at Beam Therapeutics and Foghorn Therapeutics, where responsibilities included submission management, Veeva RIM implementation, and collaboration with cross-functional teams. Steve's expertise includes extensive experience with FDA submissions and regulatory requirements, having also contributed to key projects at companies such as Blueprint Medicines, Wave Life Sciences, Sage Therapeutics, Alnylam Pharmaceuticals, Cubist Pharmaceuticals, and Genzyme Corporation. Steve holds an Associate in Applied Science degree in Industrial Design from Wentworth Institute of Technology.