Senior CMC Regulatory Affairs Director — FDA Pathways Lead

A biotechnology company in Redwood City is seeking an experienced Associate Director/Director of CMC Regulatory Affairs. This role will lead regulatory activities for the ECO Synthesis platform and will engage with the FDA's Emerging Technologies Program to secure advanced manufacturing designations. The ideal candidate should have over 8 years in CMC regulatory affairs with strong knowledge of GMP and experience in regulatory submissions.

This position offers competitive benefits including comprehensive healthcare and generous paid time off.
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