Fate Therapeutics, Inc. is seeking a highly motivated Scientist of Quality Control (QC) with ddPCR and other molecular assay experience to support its cellular therapy programs. This role will focus primarily on ddPCR analytical methods and will also cross-train on flow cytometry and cell based analytical methods. This role will be responsible for providing oversight and support for execution, optimization, transfer, qualification, and validation of analytical methods supporting manufacturing in-process control (IPC) and lot release of product, within a Good Manufacturing Practices (GMP) environment. The successful candidate will have experience participating in high performing teams executing analytical test methods, working with mammalian cell culture, analyzing emerging data to assess the characteristics of hematopoietic and stem cell-based therapeutics, and GMP method qualification and validation. This role requires extensive interaction with Research & Development, Quality Assurance, Program Management, Regulatory Affairs, Technical Operations, and Contract Manufacturing Organizations (CMOs). This is a full-time position located at our corporate headquarters in San Diego, CA.