Medical Device Regulatory Affairs Associate — Global Submissions

A leading medical device company in Lake Forest, IL, is seeking a Regulatory Affairs Associate to assist with U.S. and global regulatory submissions. The role involves preparing technical documentation, supporting regulatory strategies, and ensuring compliance with FDA and EU requirements. Candidates should possess a Bachelor’s degree and direct experience in medical device regulatory affairs. This position offers a full-time schedule from Monday to Friday, with a duration of 12 months and possible extension. #J-18808-Ljbffr