Kellie Stefaniak serves as the Vice President of Global Regulatory and Quality. In this role, she leads all global Regulatory, Quality and Clinical Affairs functions at Bioventus. Kellie has more than 25 years of experience in the Medical Device industry, in progressive leadership roles at companies including Abbott, Allergan Medical, and Bausch & Lomb. She is highly experienced in combining scientific, regulatory, and business knowledge to create strategies for new product development and sustaining activities.
Kellie graduated Summa Cum Laude from the New York Institute of Technology, earning her Bachelor of Science degree in Behavioral Science, Psychology. She also completed the RAPS Executive Development Program at the Kellogg School of Management at Northwestern University.
