Remote Senior Associate Director, CMC Regulatory Affairs

Artiva Biotherapeutics Inc. in San Diego, CA seeks an Associate Director of Regulatory Affairs, CMC to lead late-stage regulatory submissions and lifecycle activities for our NK cell therapy programs.

You will author Module 3/CTD content, coordinate with QA, Process Development, Manufacturing, and Clinical teams, and interact with FDA, EMA, and ex-US authorities to ensure compliant, timely filings. This role combines scientific rigor with strategic regulatory leadership.