Global Regulatory Strategy Lead, Medical Devices

A global health-tech leader is seeking a Principal Regulatory Affairs Specialist to lead and influence regulatory strategies ensuring compliance for medical devices. The role requires 8+ years of experience in FDA regulated environments and expertise in regulations related to hardware and software. You will mentor other professionals and provide strategic guidance on lifecycle management while enhancing safety and efficacy of medical devices. This role supports a hybrid working environment with onsite requirements at least three days per week. #J-18808-Ljbffr