Job Code 301LR
Fate Therapeutics is seeking an experienced and motivated Senior Manager or Associate Director of Quality Assurance to support Fate’s internal and external cGMP manufacturing operations. The successful candidate must thrive in a fast-paced team environment, have excellent communication, planning and organizational skills, and manage quality assurance activities to meet Fate’s priorities and timelines. The candidate must have experience and a proven track record of establishing and maintaining a quality management system to support GXP-compliant manufacturing operations and will be expected to effectively follow Fate’s SOPs and policies. This is a full-time position reporting to the Quality Assurance Associate Director and is located at our corporate headquarters in San Diego, California.
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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.