Regulatory Affairs Manager

Location: North Haven, Connecticut, United States of America

We anticipate the application window for this opening will close on - 4 Nov 2026

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

A Day in the Life

As the Regulatory Affairs Manager, you will be responsible for establishing strategies for worldwide product approval and submission activities, directly executing submission activities focused on the U.S. and EU, and ensuring regulatory compliance for products within the Surgical Operating Unit. The Regulatory Affairs Manager is expected to achieve results through hands-on leadership and the delegation of responsibilities to individual contributors. This role requires collaboration with business partners to develop regulatory strategies that support business goals and translate those strategies into work plans for the Regulatory Affairs teams.

This position requires working onsite four days per week at one of our Surgical locations: North Haven, CT (preferred), Lafayette, CO, Mounds View, MN or Mansfield, MA.

Responsibilities may include the following, as well as other duties that may be assigned.

Additional Locations: Boston, Massachusetts, United States of America