Global Regulatory Affairs Lead — Medical Devices (Onsite 4x/wk)

Medtronic in Lafayette, CO is seeking a Regulatory Affairs Manager to establish strategies for worldwide product approval and submission activities, focusing on U.S. and EU regulatory compliance for Lung Health and Gynecologic devices. The role requires onsite work four days a week at specified Surgical locations and leadership of cross-functional regulatory teams to meet business goals and regulatory timelines.