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AbbVie Inc. is seeking a seasoned professional to lead global CMC submission activities for biologics, coordinating cross-functional teams to ensure high-quality regulatory documents. The role emphasizes alignment with clinical development strategy and timely responses to authorities. Responsibilities include mentoring dossier authors, developing submission templates, and mitigating regulatory risks while maintaining strong external collaborations and internal leadership.

Also on the board Same function, level within a rung

Level

Manager

Location

Chicago, IL

Occupation

Regulatory Affairs Managers

Industry

Pharmaceutical Preparation Manufacturing

Posted

today

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