Global Regulatory Affairs Lead – Medical Devices

A global medical technology company is seeking a Senior Regulatory Affairs Specialist to lead global regulatory strategies and submissions for their Orthopaedics portfolio. This role, based in Memphis, TN, requires at least 5 years of experience in regulatory affairs within the medical device sector. Responsibilities include preparing regulatory submissions, managing compliance, and leading projects within a collaborative environment. The position offers competitive compensation and benefits, promoting work-life balance and wellbeing. #J-18808-Ljbffr