Regulatory Affairs Specialist — Global Medical Devices

A leading medical technology company located in Tempe, Arizona is seeking a Regulatory Affairs Specialist to provide primary regulatory support for product lines. The role involves preparing regulatory submissions, ensuring compliance, and guiding teams on regulatory requirements. Qualified candidates should have a Bachelor’s degree in a relevant field and at least one year of experience in regulatory affairs within the medical device industry. The position emphasizes detail-oriented work with a focus on communication and problem-solving abilities. #J-18808-Ljbffr