Global CMC Regulatory Lead - Late-Stage Submissions

A leading pharmaceutical company is looking for a CMC Global Regulatory Affairs professional to develop and execute regulatory strategies for small molecules during late-stage development and throughout the commercial lifecycle. Responsibilities include ensuring compliance with global regulations, planning regulatory submissions, and representing CMC Regulatory Affairs in project teams. The role requires significant experience in regulatory affairs and strong analytical, leadership, and problem-solving skills.

This position also involves approximately 20% travel.
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