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

📋 Description

• The Senior Associate RA CMC is responsible for ensuring RA-CMC post approval change objectives are
• Communicate with key partners in functional departments to support regulatory filings.

🎯 Requirements

• BA/BS in Chemical and/or Biological Sciences or relevant discipline
• 4 years pharmaceutical/industry experience; 1-2 years in quality systems or cross-functional
• 5 years pharma experience including 1-2 years in regulatory affairs or 1-2 years in Discovery
• Strong knowledge of manufacturing unit operations or CTD structure
• Excellent oral and written communication; ability to work with global teams
• Experience with electronic document management systems; ability to manage multiple projects

🎁 Benefits

• AbbVie benefits package including paid time off, medical/dental/vision insurance, and 401(k)
• Eligibility to participate in short-term incentive programs
• AbbVie is an equal opportunity employer