Teams at MaxCyte, Inc.

Conduct genomic safety research for CRISPR gene-editing therapeutics, including off-target discovery, genome integrity assessment, assay development, validation, and NGS workflows. Maintain and optimize human cell culture and gene-editing studies, operate laboratory automation and sequencing equipment, analyze data, and support client studies. Author SOPs and validation documents, manage quality events and CAPAs, improve laboratory workflows, and train junior scientists.