Global Regulatory Affairs Specialist - Medical Devices

Terumo Medical Corporation seeks a Regulatory Affairs Associate positioned in New Jersey to manage the regulatory requirements for medical devices. The role involves preparing required documents and submissions to obtain clearance for products. Ideal candidates will possess strong organizational skills, in-depth knowledge of regulatory requirements, and a background in life sciences or engineering. This position demands proactive contributions to the growth of the regulatory affairs department and interaction with various internal and external parties. #J-18808-Ljbffr