Global Medical Device Regulatory Affairs Associate II

A medical device company located in California is seeking a Regulatory Affairs Associate II. This role involves providing regulatory support for U.S. and global submissions, executing regulatory strategies, and ensuring compliance for product approvals. Ideal candidates will have 2-4 years of experience in Regulatory Affairs, especially within the medical device industry, as well as knowledge of FDA submissions and global requirements. Excellent communication and project management skills are essential. #J-18808-Ljbffr