Global Regulatory Affairs Specialist, Medical Devices (PMA)
Synergy Spine Solutions Inc.
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 #J-18808-Ljbffr Synergy Spine Solutions Inc.
Vacancy posted 1 day ago
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