Senior Regulatory Affairs Lead: FDA Submissions & Compliance

A global biopharmaceutical services company is seeking a Senior Regulatory Affairs Associate in Little Rock, Arkansas. This role focuses on leading regulatory processes and ensuring compliance with FDA regulations. The ideal candidate will have 3–5 years of regulatory experience and a strong background in project management. Key responsibilities include documentation preparation, regulatory submissions, and supporting audits. The position offers a dynamic work environment and collaboration with various internal teams to drive regulatory strategies. #J-18808-Ljbffr