Lilly is seeking a Director, GRA-CMCD Lifecycle Innovation to provide scientific, strategic, and operational regulatory leadership for post-approval CMC activities across Lilly's parenteral product portfolio. This role drives lifecycle strategies, data package quality, and timely submissions with global teams across sites and CMOs. Responsibilities include leading variations, assessing changes, coordinating with Manufacturing and Quality, and mentoring regulatory staff to ensure compliant,

Also on the board Same function, level within a rung

Level

Manager

Location

Indianapolis, IN

Occupation

Regulatory Affairs Managers

Industry

Pharmaceutical Preparation Manufacturing

Posted

yesterday

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