Senior Director of Technology, Quality & Regulatory
Christie has responsibility for technical engineering, quality, and regulatory functions for Vonco Products. Christie joined Vonco Products in March 2019. She has extensive experience with quality and regulatory requirements in the medical device industry. Christie completed her Bachelor of Science Degree in 2009, maintains multiple ASQ Certifications (CMQ/OE, CQE, CQA), and holds a Leadership Certificate from Cornell University. Prior to joining Vonco Products, Christie worked with large companies in the medical device industry – Viant Medical, Vyaire Medical (formerly CareFusion), and Hollister Incorporated. These certifications and work experience have allowed Christie to guide Vonco’s path as we expand our capabilities into regulated industries. Christie was instrumental in the upgrade of Vonco’s quality management system to meet the requirements of ISO 13485:2016 and has navigated through the FDA 510(k) Premarket Notification process for Vonco’s first Class 2 medical device. She has provided guidance in our design and development process to drive Vonco to success when designing, validating, and integrating new products into the Vonco portfolio. When facing customers, we lead with the ‘risk free’ approach of Quality, Technical Innovation and Fast Custom Development. Christie plays a significant role in guiding/supporting the team that helps Vonco continue to deliver on this promise. Christie’s background and knowledge allow her to provide direct guidance to Vonco in support of our Leak Proof Guarantee and medical device contract manufacturing initiatives. Christie resides in Salem, WI. In her free time, she enjoys traveling, golfing, training with her German Shepherds, and live music.