Job Code 382MW
Fate’s Quality Assurance (QA) group is seeking a motivated and talented individual to support clinical-stage development quality assurance activities. This role will work cross-functionally to execute and improve the material control and supplier quality management program and ensure compliance and assess risk and quality of materials used in the development of clinical stage cell therapy products. The successful candidate will assure adherence to standard operating procedures, GXP guidelines, and applicable regulations. Experience working in a cGMP environment is a must and candidates must thrive in a fast-paced team environment and have excellent attention to detail, communication, organizational, and independent problem-solving skills. This is a full-time position reporting to the Associate Director, Quality Assurance, and is located at our company’s headquarters in San Diego, California.
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For consideration send cover letter and curriculum vitae to: email@example.com and reference job 382MW.
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.