Global Regulatory Affairs Specialist
Listed on 2026-09-30
-
Quality Assurance - QA/QC
Aspen Surgical is seeking a Regulatory Affairs Specialist, International, in Caledonia, MI. You will prepare and submit regulatory filings for U.S. and global markets, and organize STED documentation to support registrations.
You will coordinate international activities for customers and partners, review technical data, and help maintain ISO/CE compliance. You will work with R&D and QA teams to identify regulatory needs, track changes, and support post‑market activities including vigilance
We are currently recruiting a Global Regulatory Affairs Specialist for our team in MI, United States.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Global Regulatory Affairs Specialist role in the description above.
We appreciate your interest in this position.
Join Aspen Surgical and contribute to our ongoing work.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).