Teams at Beam Therapeutics

Provides Quality oversight for laboratory, manufacturing, QC, and facilities operations at a cell and gene therapy manufacturing site. Responsibilities include shop-floor presence, batch and logbook review, GMP compliance, product disposition, deviation and CAPA approval, work-order and asset approvals, quality-system improvements, tech transfers, equipment qualification and validation, issue resolution, metrics, and regulatory inspection support. Requires onsite work and a flexible schedule, including alternate shifts.

Leads Beam Therapeutics’ Massachusetts GMP Quality Control organization, overseeing release, stability, method qualification, validation, and transfer testing. Manages QC staff, laboratory investigations, deviations, change controls, CAPAs, data integrity, equipment and system readiness, training, inspection preparation, and continuous improvement. Partners cross-functionally to support clinical manufacturing, commercial and BLA readiness, regulatory inspections, and compliant laboratory operations.

Administer and enhance Beam’s LabVantage LIMS, LES, SDMS, instrument integrations, Attachment Handler configurations, and laboratory automation systems. Partner with QC, QA, IT, validation, and laboratory scientists to digitize workflows, manage data integrity, support integrations, troubleshoot issues, and deliver compliant GMP and non-GMP solutions. Support CSV, GAMP 5, 21 CFR Part 11, audits, inspections, documentation, training, governance, and continuous improvement.