Associate Director, CMC Regulatory Strategy & Submissions

A biotechnology firm in California is seeking an experienced Associate Director/Director of CMC Regulatory Affairs to lead regulatory activities for their ECO Synthesis platform. The role involves developing regulatory strategies, preparing submissions such as INDs and DMFs, and collaborating with cross-functional teams to ensure compliance with FDA and global standards. Candidates should have an advanced degree in life sciences and over 8 years of relevant experience.

The position offers an opportunity to influence regulatory pathways for innovative therapeutic technologies.
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