Associate Director, Quality Control

Role: Associate Director, Quality Control at Beam Therapeutics, leading GMP testing operations for clinical and late-stage programs in gene editing therapeutics. Responsibilities: oversee routine GMP testing (release, stability, validation, transfer), ensure laboratory and data systems compliance, manage QC staff, lead investigations and CAPAs, maintain inspection readiness, and support regulatory interactions. Qualifications: advanced degree in a relevant scientific discipline; 8+ years in QC within biologics, cell or gene therapy, or complex modalities; proven leadership in GMP QC labs; strong knowledge of GMP operations, data integrity, and quality systems; experience supporting inspections. HighValue: biologics/gene therapy, GMP QC, regulatory inspection readiness, data integrity, cross-functional collaboration with QA, manufacturing, R&D, and regulatory teams. Work setup: on-site in Cambridge, MA; no travel specified.