Global Medical Device Regulatory Strategist
Listed on 2026-09-16
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Healthcare
Healthcare Compliance, Medical Science Liaison, Medical Device Industry
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
Our team is growing, and we are hiring a Global Medical Device Regulatory Strategist in MI, United States.
Join Everis and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the Global Medical Device Regulatory Strategist role at Everis, based in MI, United States.
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