Global Regulatory Affairs Specialist, Medical Devices

A global medical technology company is seeking a Regulatory Affairs Specialist in Tempe, Arizona. You will provide primary support for regulatory submissions and compliance processes for medical devices. The role entails participating in product development teams, reviewing product changes, and ensuring regulatory adherence across global markets. Ideal candidates will have a Bachelor’s degree in a technical field and experience in the medical device industry. Travel may be required up to 25%. #J-18808-Ljbffr