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. Preparation of document packages for international regulatory submissions from all areas of company, internal audits and inspections.

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-clinica...