Senior RA-CMC Lead for Post-Approval Changes

AbbVie in North Chicago, IL is seeking an experienced Regulatory Affairs - CMC professional to independently manage post-approval variation dossiers and author CMC sections. This role will ensure timely preparation of submission documents and coordinate with cross-functional partners globally.

You will lead, coach, and develop junior staff, drive programs across multiple post-approval changes, and ensure CTD content and formatting standards are met across projects.