Senior Associate, Regulatory Affairs - Chemistry, Manufacturing & Control (CMC) - Hybrid

📋 Description RA-CMC post approval change objectives met by project managing marketed product variations. Authoring and compilation of chemistry, manufacturing, and control (CMC) sections for submissions. Coordinate with key partners in the functional departments to support regulatory filings. Hybrid schedule: 3 days in office and 2 days remote from AbbVie locations. 🎯 Requirements BA/BS in Chemical and/or Biological Sciences or related field. 4 years pharmaceutical or industry-related experience; 1–2 years in quality systems or 5 years pharmaceutical experience with 1–2 years in regulatory affairs or related areas (Discovery Strong knowledge of manufacturing unit operations or CTD structure. Excellent oral/written communication; ability to work with global teams and with electronic Ability to manage multiple projects independently and under pressure; detail-oriented. 🎁 Benefits Competitive compensation package; salary range $84,500–$162,000 per year. Comprehensive benefits including PTO, health/dental/vision, and 401(k). Equal opportunity employer; includes Veterans/Disabled; relocation/visa sponsorship details vary by