Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.

If you are passionate about regulatory affairs and want to play a meaningful role in bringing medical device innovation to patients around the world, this is an opportunity to build your expertise within a collaborative and supportive global environment. As a Regulatory Affairs Specialist 2, you will work across regions, products and teams, contributing directly to the success of our orthopaedics portfolio and helping ensure our technologies meet regulatory requirements worldwide.

What will you be doing?

In this role, you will be part of a collaborative regulatory affairs team supporting both new and existing medical devices. Your work will span global regulatory submissions and sustaining activities for our legacy orthopaedic portfolio. You will partner closely with project teams to shape regulatory strategies, support product changes and maintain ...