Full-time Posted June 24, 2026
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Job Description

Position Summary You will lead Chemistry, Manufacturing and Controls (CMC) regulatory strategy for development and lifecycle activities. You will work with cross‑functional teams across development, manufacturing, quality and regulatory to prepare submissions and respond to regulatory requests. Your work will directly support timely access to medicines and continued supply for patients. Responsibilities Drive the CMC strategy, coordinate timely preparation and authorship of technical (CMC) regulatory documents, and identify risks to submission data and package, providing well‑defined mitigation strategies. Mentor or train staff; manage project activities for multiple complex projects and teams, providing strategic direction, data assessment and conclusions within and across departments. Engage and lead CMC Subject‑Matter‑Expert activities internally and externally to improve compliance, harmonisation and efficiency. Deliver CMC regulatory strategy to support major inspections or qualit...

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