from a U.S. law school; Current admission to any state bar in good standing (admission to Washington, California, or Massachusetts strongly preferred); 10+ years of professional experience as an attorney; Comprehensive knowledge of biologic and drug development process, pharmaceutical technology, manufacturing processes, GMP, quality assurance & management and related issues, preferably in the areas of cell and gene therapy; Proven knowledge of CMC regulatory submission requirements for global filings (FDA and/or EMA, etc.). Act as the primary legal subject matter expert, reference and point-of-contact for the Technical Operations functions at Sana, including Manufacturing, Quality, Process Development, Supply Chain & CMC Portfolio, External Manufacturing, External Supply & Procurement, CMC Regulatory Affairs, Analytical Development & Operations and other Technical Operations teams.