Regulatory Affairs Associate II — Global Submissions Lead

A global regulatory consulting firm seeks a Regulatory Affairs Associate II to support US and international submission requirements. The role involves regulatory strategy execution and compliance oversight. Candidates should have 2-4 years of experience in the medical device industry and a strong understanding of FDA regulations. This position offers a hybrid work arrangement, with locations in Lake Forest, San Clemente, or San Diego. #J-18808-Ljbffr