Susan Walden

Susan Walden is an experienced regulatory affairs professional with over 28 years in the medical device industry, primarily at Medtronic and Mozarc Medical. Most recently serving as a Regulatory Affairs Operations Program Manager at Mozarc Medical, Susan led process improvements and developed systems to enhance regulatory submissions and product release activities for international markets. During a notable tenure at Medtronic, Susan held various roles, including Principal Regulatory Operations Specialist and Regulatory Affairs Manager, where responsibilities encompassed managing submissions, developing quality SOPs, and participating in regulatory transformation efforts. Susan holds a Bachelor of Arts in Organizational Leadership from Bethel University, earned between 2000 and 2002.