Job Code 375AL
Fate Therapeutics, Inc. is seeking a highly motivated Quality Control (QC) Scientist with flow cytometry, qPCR, and/or cell-based assay experience to support its expanding cellular therapy programs. This role will support execution, optimization, transfer, qualification, and validation of methods for manufacturing in-process control (IPC), lot release, and stability testing of clinical drug product within a Good Manufacturing Practices (GMP) environment. The successful candidate will be adept at 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 is a full-time position located at our corporate headquarters in San Diego, CA reporting to the Associate Director, Quality Control.
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About Fate Therapeutics, Inc.
Fate Therapeutics is a biopharmaceutical company dedicated to the development of programmed cellular immunotherapeutics for the treatment of cancer and immune disorders. The Company’s cell-based product candidate pipeline is comprised of off-the-shelf immuno-oncology therapeutics, including NK- and T-cell-based candidates derived from induced pluripotent cells, and immuno-regulatory therapeutics, including hematopoietic cell-based candidates for protecting the immune system of patients undergoing hematopoietic cell transplantation and for suppressing auto-reactive T cells of patients with auto-immune disorders. Its adoptive cell therapy candidates are based on the Company’s novel ex vivo cell programming approach, which it applies to modulate the therapeutic function and direct the fate of immune cells.