Global Medical Device Regulatory Strategist

Everis is seeking a Regulatory Specialist to obtain and maintain regulatory approvals for medical devices in international markets, ensuring ongoing compliance with FDA, ISO 13485, and global standards. You will collaborate with R&D, QA, Clinical, Manufacturing, Marketing, and Supply Chain to manage submissions, lifecycle activities, and post-market obligations while monitoring regulatory changes.

This role involves coordinating with distributors and authorities to facilitate registrations and

We are seeking a motivated Global Medical Device Regulatory Strategist to join Everis in MI, United States.

The position is based in MI, United States.

This opportunity is part of our work in Legal, Management & Operations.

The advertised compensation is 65.000 - 95.000.

We aim to respond to suitable candidates as soon as possible.

Full responsibilities and requirements are described in the listing above.