Regeneron Pharmaceuticals, Inc seeks an Associate Director in Uxbridge to lead global CMC regulatory strategies for hematology and oncology portfolios. The role requires on-site work three days a week, with some remote collaboration. Candidates should have a minimum of 10 years of industry experience, including 5+ years in CMC, and a proven track record in regulatory interactions.
You will be responsible for regulatory strategy development, mentoring staff, and ensuring compliance throughout the drug development process. This is an excellent opportunity to join a company committed to building an inclusive work culture.
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