Global Regulatory Affairs Lead — Medical Devices; Onsite
Listed on 2026-10-09
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Healthcare
Healthcare Compliance, Healthcare Management
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.
As a Global Regulatory Affairs Lead — Medical Devices (Onsite 4x/wk), you will play an important part at Medtronic in Lafayette, CO, United States.
This is a strong opportunity to take on the Global Regulatory Affairs Lead — Medical Devices (Onsite 4x/wk) role at Medtronic.
We invite applications for the Global Regulatory Affairs Lead — Medical Devices (Onsite 4x/wk) position located in Lafayette, CO, United States.
The following role is for a Global Regulatory Affairs Lead — Medical Devices (Onsite 4x/wk) with Medtronic.
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