Hybrid CMC Regulatory Specialist — CTD/eCTD Expert

A prominent pharmaceutical company is seeking a Regulatory Affairs Specialist to support regulatory submissions with a focus on Chemistry, Manufacturing, and Controls (CMC). This role involves authoring and reviewing Module 3 content for CTD and eCTD submissions. The ideal candidate will have 1-2 years of experience in the pharmaceutical industry and a Bachelor's or Master's degree in Chemical Sciences. Strong communication skills and knowledge of ICH guidelines are essential for success in this hybrid role based in North Chicago, IL. #J-18808-Ljbffr