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Smeet Doshi M.S. is a highly experienced regulatory affairs professional specializing in medical devices, currently serving as a Senior Regulatory Affairs Specialist at Zimmer Biomet since November 2022, leading new product introduction and development within the Craniomaxillofacial and Thoracic Division. Prior experience includes a role as Regulatory Affairs Specialist at Medtronic Brain and Spine Therapies, where Smeet received the Global Regulatory Affairs Excellence Award for FY2022, and contributed to the preparation and submission of various regulatory documents. Previous positions include Regulatory Affairs Operations Specialist at Endologix LLC, where Smeet designed technical documentation for Class III products, and multiple internships focused on regulatory strategy and compliance in medical device fields. Smeet holds a Master of Science in Medical Devices and Diagnostic Engineering from the University of Southern California and a Bachelor of Engineering in Biomedical Engineering from the University of Mumbai.