UCB is seeking a Global Regulatory Affairs CMC Lead - Early Development to shape global regulatory CMC strategies for early-development biologics. You will collaborate with cross-functional teams across regions to plan, author and submit high-quality regulatory documentation and engage health authorities to enable timely approvals.
Based in a hybrid setup with offices in Slough, Brussels or Raleigh/Atlanta as possible, you will monitor regulatory changes, coach colleagues, and drive lifecycle
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London
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