Director of Quality Assurance and Regulatory Affairs
Candice is the Quality Assurance and Regulatory Affairs Director responsible for ensuring the product we develop and manufacture meets our customer’s needs, The product is manufactured to high standard and complies to the regulations for the markets we sell into. Her goal is to drive a quality culture where we strive to be a world class organization, with customers who return to Dynex for the experience they have had with our products and services.
Candice is an experienced Quality Assurance & Regulatory Director specializing with the in vitro Diagnostic Medical Devices and has been involved with all aspects of product life cycle from initial design through to clinical studies, 510(k) and registrations of products into the Americas, Europe, China, Australia and emerging markets. She joined Dynex in January, 2014 with over 15 year’s direct Medical Device experience.