Global Regulatory Affairs Leader, Medical Devices
Listed on 2026-10-07
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Business
Regulatory Compliance Specialist
Rauland, a division of AMETEK, seeks a Sr. Manager, Regulatory Affairs to lead the global regulatory function and ensure compliance with FDA, EU MDR, and other international requirements. You will shape regulatory strategy across product development, market access, and lifecycle management.
You will oversee submissions and registrations, advise cross‑functional teams, drive post‑market activities, audits, and continuous improvement, while building a high‑performing regulatory organization.
Step into the Global Regulatory Affairs Leader, Medical Devices role at AMETEK in Mount Prospect, IL, United States and grow with us.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Mount Prospect, IL, United States.
This opportunity is part of our work in Legal, Management & Operations.
The advertised compensation is 175..
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