Advita Ortho, LLC seeks a Director of Post Market Surveillance and Clinical Affairs to lead the integrated post-market quality assurance and clinical affairs functions in Gainesville, FL. You will drive compliance, evidence planning, PMCF, and regulatory reporting to support product safety and lifecycle decisions.
The role requires extensive FDA/ISO-regulated medical device experience, leadership of cross-functional teams, and strong technical writing skills, with a focus on risk management and
#J-18808-LjbffrSenior Director, Post-Market Surveillance & Clinical Strategy in gainesville at Unknown Company
This position is listed as full time and onsite.