Director, CMC Regulatory Affairs — Global Submissions

A biopharmaceutical company is seeking a Director of Regulatory Affairs CMC to lead regulatory strategies and manage submissions for candidate projects. The ideal candidate will have at least 10 years of experience in the biopharmaceutical industry, preferably in a biotech environment. Responsibilities include developing CMC regulatory strategies, representing the company to regulatory agencies, and ensuring compliance. Successful candidates will demonstrate excellent leadership and communication skills.

This position is located in San Diego, California.
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