Global Regulatory Affairs Specialist, Medical Devices; PMA)
Listed on 2026-10-06
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Quality Assurance - QA/QC
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Healthcare
Synergy Spine Solutions is seeking a mid-level Regulatory Affairs Specialist to support the global regulatory lifecycle of the Synergy Disc and future motion-preservation technologies. This on-site role in Louisville, CO connects R&D, Quality, Clinical, and commercial teams to maintain approvals across markets.
You will author and compile regulatory submissions, manage PMA/IDE pathways, monitor EU MDR and global standards, and drive post-approval commitments with meticulous attention to detail
We have an opening for a Global Regulatory Affairs Specialist, Medical Devices (PMA) in Louisville, CO, United States within Legal, Management & Operations.
Join Synergy Spine Solutions Inc. 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 Regulatory Affairs Specialist, Medical Devices (PMA) role at Synergy Spine Solutions Inc., based in Louisville, CO, United States.
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