Rhythmlink in Columbia, SC is seeking a Senior Regulatory Affairs Specialist to lead regulatory activities for new product development and lifecycle management, including cross-functional collaboration with engineering, quality, and clinical teams.
You will develop EU MDR technical documentation, manage 510(k) submissions, and monitor global regulatory requirements to maintain market authorizations and ensure audit-ready records.
#J-18808-LjbffrSenior Medical Device Regulatory Lead in columbia at Unknown Company
This position is listed as full time and onsite.