Medical Device Regulatory Affairs Associate – Hybrid (12mo)

A medical device company is seeking a Regulatory Affairs Associate II in San Diego, California. The role requires hands-on regulatory experience with FDA submissions and EU MDR compliance. You will manage regulatory submissions, maintain Technical Documentation, and interact with regulatory bodies. The position offers a hybrid work schedule, making it an ideal opportunity for professionals with a background in medical device regulations. This contract position may convert to full-time employment based on performance. #J-18808-Ljbffr