Regulatory Affairs Specialist

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

**A Day in the Life**
Supporting Design and Development Control activities with regulatory requirements, direction, tactics and strategies and working in a team environment with all organizational departments.

**Responsibilities may include the following and other duties may be assigned:**

+ Prepare, review, file, and support premarket documents for global registrations for assigned projects.
+ Collaborate with business unit and international regulatory affairs personnel to support marketing authorizations for assigned projects.
+ Review pre-clinical, and clinical protocols and associated reports to be used in submissions for assigned projects.
+ Develop Regulatory Strategies for new or modified products for ...

Ready to Apply?

Submit your application today and join our talented team at Medtronic.

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