Job Code 311MW
Fate’s Quality Assurance (QA) group is seeking a motivated and talented individual to support development and implementation of the Document Control program. The successful candidate will assure adherence to standard operating procedures, GXP guidelines, and applicable regulations. The ideal candidate will have experience working in a cGMP environment, and have hands-on experience in document management, change control, and training. Candidates must thrive in a fast-paced team environment and must have excellent attention to detail, communication, organizational abilities, and independent problem-solving skills. This is a full-time position reporting to the Senior Manager, Quality Assurance, and is located at our company’s 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.