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Gino Rouss has extensive experience in the field of regulatory affairs, with a focus on medical devices. Gino currently holds the position of Vice President of Regulatory Affairs and Quality at uLab Systems, Inc. Prior to this role, they served as the Senior Director of Regulatory Affairs at MicroPort Orthopedics, where they were responsible for the development and implementation of products under the new EU Medical Device Regulations (MDR). Gino also worked at Medtronic, where they held various roles including Senior Director of Regulatory Affairs, overseeing global regulatory activities and managing product submissions to Health Authorities. Earlier in their career, Gino held positions at Smith & Nephew, where they served as the Group Manager, Manager, and Program Manager of Regulatory Affairs, leading the development of regulatory strategies and managing day-to-day activities. Overall, Gino has demonstrated their expertise in regulatory compliance, strategy development, and successful product approvals in various markets.

Gino Rouss holds a Bachelor of Science (BS) degree in Mechanical Engineering from The University of Memphis. Gino further pursued their education and obtained a Master of Science (MS) degree in Mechanical Engineering from the same institution.