Teams at LEXEO Therapeutics

Leads CMC Quality Control oversight for gene therapy programs, including external laboratory management, analytical method lifecycle activities, stability and release testing, investigations, specifications, reference standards, comparability, and regulatory submissions. Partners with Analytical Development, Technical Operations, Regulatory Affairs, Quality Assurance, and external vendors to support clinical development, process validation, and commercial readiness. Coordinates sample submissions, shipments, and testing activities while ensuring cGMP and global regulatory compliance.