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Regulatory Affairs CMC Associate Director (Biologics)
583! That is the total number of projects and products on our Global Regulatory Affairs CMC project list. All of these innovative projects are aimed at making a difference in patients' lives and we need your help. As a member of our Global Regulatory Affairs CMC team, your role would be to establish and drive global CMC regulatory strategic and operational direction and documentation for projects and products covering development, registration and approval/post approval activities. **There are multiple positions available** Your Responsibilities include but are not limited to: * Formulate, lead and drive global CMC regulatory strategy for Biologics modality projects/products drawing on substantial regulatory expertise with a focus on innovation, maxim


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