Job Code 254JB
Fate Therapeutics, Inc. is seeking an experienced and highly motivated regulatory professional to support Regulatory Affairs Operations. This is a full-time position reporting to the Executive Director, Regulatory Affairs. This position will be responsible for operational aspects of all regulatory submissions, ensuring that the submissions are of the highest quality and submitted on-time. The position will also support the compilation, archiving, and tracking of regulatory submissions and health authority correspondence in partnership with Regulatory Program Management, cross-functional Teams, and external partners. Emphasis will be on strategic planning, management, and execution of all aspects of Regulatory Affairs Operations.
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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.