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