Manager, Regulatory Affairs for Chemistry Manufacturing & Controls (CMC)

📋 Description

• Hybrid work schedule (3 days in office) at AbbVie Lake County, IL; Irvine, CA or Waltham, MA
• Prepares CMC regulatory strategies to enable first pass approvals; manages content for regulatory
• Represents RA CMC on product development and lifecycle teams; negotiates with and informs peers to
• Interacts with RA, R&D and Operations to ensure regulatory compliance and timely submissions.

🎯 Requirements

• Bachelor’s degree in pharmacy, biology, chemistry, pharmacology, engineering or related field.
• 6 years biopharmaceutical or related industry experience; 3 years in regulatory affairs preferred.
• Strong oral and written communication; ability to work in a complex, matrix environment.

🎁 Benefits

• AbbVie offers a comprehensive package of benefits including PTO, medical/dental/vision insurance
• Eligible to participate in long-term incentive programs.