Tim White

Tim White is a seasoned professional with extensive experience in regulatory affairs and quality management within the medical device industry. Currently serving as the Regulatory Affairs Manager at Centrix Inc., Tim White oversees compliance with EU MDR, FDA, and Health Canada regulations, along with various ISO standards. Previously, Tim White held the position of Senior Quality Manager at Viant Medical, managing a 22-member quality department and ensuring compliance with FDA QSR/GMP and ISO 13485. Tim White's career spans multiple roles, including Medical Device Quality Assurance & Regulatory Affairs Management at Abrasive Technology and Manufacturing Manager at Carlisle FoodService Products, showcasing a strong background in quality systems, process improvement, and leadership in high-volume manufacturing settings. Tim White holds an MBA from The Ohio State University Fisher College of Business and a B.S. in Ceramic Engineering from Alfred University.