Jim Taufen
About Jim Taufen
Jim Taufen serves as the Director of Regulatory Affairs at AtriCure, Inc., a position he has held since 2018. He has extensive experience in regulatory affairs, having previously worked at Smiths Medical and Boston Scientific.
Work at AtriCure
Jim Taufen has served as the Director of Regulatory Affairs at AtriCure, Inc. since 2018. In this role, he oversees regulatory compliance and strategy for the company, ensuring that products meet all necessary regulations and standards. His tenure at AtriCure includes a previous position as Director of Regulatory Affairs from 2015 to 2016, where he contributed to the regulatory processes in both Minnetonka, MN, and West Chester, OH.
Previous Experience in Regulatory Affairs
Before his current role at AtriCure, Jim Taufen worked as the Director of Regulatory Affairs at Smiths Medical from 2016 to 2018. His responsibilities included managing regulatory submissions and compliance for medical devices. Prior to that, he spent 11 years at Boston Scientific as Regulatory Affairs Manager II, where he was involved in regulatory submissions and product approvals from 2004 to 2015 in Arden Hills, MN.
Education and Expertise
Jim Taufen earned a Bachelor of Science degree in Education from the University of Minnesota. His educational background in Biology supports his expertise in regulatory affairs, particularly in the medical device industry. This foundation has equipped him with the knowledge necessary to navigate complex regulatory environments.
Career Timeline
Jim Taufen's career in regulatory affairs spans several years and various roles. He began his career at Boston Scientific, where he worked for 11 years before moving to Smiths Medical for two years. He then returned to AtriCure, where he has held the position of Director of Regulatory Affairs since 2018, reflecting a commitment to the field of regulatory compliance.