Global Regulatory Affairs CMC Lead — Associate Director

A leading biopharmaceutical company in Wilmington, Delaware is seeking an Associate Director of Regulatory Affairs CMC. This role involves managing CMC regulatory submissions and strategy for drug products, ensuring compliance with regulatory standards, leading meetings with stakeholders, and maintaining knowledge of relevant regulations. Candidates should have 4-8 years of experience in regulatory affairs and be fluent in Japanese and English. The position requires strong communication skills and an understanding of CMC regulations.
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