At Moffitt Cancer Center, we strive to be the leader in understanding the complexity of cancer and applying these insights to contribute to the prevention and cure of cancer. Our diverse team of over 9,000 are dedicated to serving our patients and creating a workspace where every individual is recognized and appreciated. For this reason, Moffitt has been recognized on the 2023 Forbes list of America’s Best Large Employers and America’s Best Employers for Women, Computerworld magazine’s list of 100 Best Places to Work in Information Technology, DiversityInc Top Hospitals & Health Systems and continually named one of the Tampa Bay Time’s Top Workplace. Additionally, Moffitt is proud to have earned the prestigious Magnet® designation in recognition of its nursing excellence. Moffitt is a National Cancer Institute-designated Comprehensive Cancer Center based in Florida, and the leading cancer hospital in both Florida and the Southeast. We are a top 10 nationally ranked cancer center by Newsweek and have been nationally ranked by U.S. News & World Report since 1999.
Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. Join our committed team and help shape the future we envision.

Summary

 

Quality Supervisor – Cell Therapy Quality Program Administration

H. Lee Moffitt Cancer Center is internationally recognized for our focus on personalized cancer care and translational research. The mission of Moffitt is clear, focused, and fully stated in nine words, “To contribute to the prevention and cure of cancer.” With a tradition of excellence that began with the first patient admission in 1986, dedicated Moffitt physicians, scientists, and staff members have remained committed to excellence in an atmosphere characterized by kindness, caring, and hope.

Job Summary:

The Quality Supervisor will be responsible for working with the Quality Management Manager to establish and maintain a robust Quality and Patient Safety Program in the Cell Therapy Core Facility that results in the administration of safe and effective products to patients and clinical trial participants. The Quality Management Supervisor must be able to work independently, manage the day-to-day operations of the department, and supervise the Quality Management Staff. The Quality Management Supervisor shall work with the Quality Management Manager to oversee and ensure compliance with departmental and institutional quality and patient safety policies, applicable regulations and accreditation standards of Cellular Therapy (e.g. FDA, GMP, GTP, AABB, FACT, CAP, JCAHO). Other responsibilities as assigned.

Credentials and Qualifications:

Bachelor’s Degree (required) – Medical Terminology or related biomedical science or related field Master’s Degree (preferred)— Medical Terminology or related biomedical science or related field Six Sigma Yellow Belt within 1 year of hire (required) ASCP, AMT, Six Sigma Green Belt, ASQ (preferred) Minimum five (5) years' experience in either regulated clinical and/or manufacturing laboratory (required) Minimum of three (3) years experience with GMP/GTP regulations for Human Cell and Tissue product manufacturers, biologics manufacturers and/or blood bank establishments (required) Minimum of one (1) year in a supervisory position (required) Minimum of three (3) years in a supervisory position (preferred) Knowledge of basic statistical tools for the development and analysis of quality metrics Demonstrate exceptional written and oral communication skills Experience with patient/product safety, performance improvement, project management and working with medical staff