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

H. Lee Moffitt Cancer and Research Institute is a modern facility in Tampa, Florida.  We strive to be the leader in understanding in the complexity of cancer through team science and applying those insights for human benefits.  Be part of the cure by joining Moffitt's team of over 800 research faculty scientists, career staff scientists, postdocs, graduate students and support staff dedicated to cancer research.

 

Position Highlights

Opportunity to join a National Cancer Institute (NCI) designated comprehensive cancer center focused on developing novel cellular therapies for cancer patients. Participate in cutting-edge immunotherapy clinical trials aimed at activating the immune system to combat cancer. Develop and perform assays to evaluate the safety and functionality of cellular products. Contribute to a rapidly expanding portfolio of clinical trials in the cell therapy field.

Ideal Candidate

Experience in cellular therapy or a related discipline. Proficient in cell culture techniques and aseptic processing. Working knowledge of adoptive cell therapy and immunotherapy principles. Familiarity with good documentation practices, laboratory and manufacturing standards, and quality control requirements for product release. Strong communication skills, engaged, and have the ability to collaborate effectively with the Cell Therapy Team. Demonstrated enthusiasm for contributing to cellular product manufacturing. Experience with quality control assays such as ELISA/ELLA, PCR techniques, flow cytometry, microbiology, endotoxin testing, and cell counting. Flexibility to work varied hours, including periodic weekends.

 

 

Responsibilities

Perform cellular product processing and quality control testing with minimal supervision, utilizing multiple processing, cell culture, and separation methods. Conduct qualitative and quantitative assays on cell therapy products, including flow cytometry, PCR techniques, sterility testing, cell counting, and ELISA/ELLA. Adhere strictly to facility standard operating procedures (SOPs) and policies in compliance with FDA, FACT, and CAP regulatory standards for cellular therapy production and analysis. Identify and address issues that could affect product quality or testing performance, following established SOPs when product processing or testing falls outside acceptable criteria and/or levels of performance. Handle fresh and frozen cellular products for shipment and infusion. Maintain aseptic technique and operate within a cleanroom environment. Perform other duties as assigned. Adapt to flexible work schedules, including, but not limited to, shift adaptability and occasional weekend shifts based on production demands.

Credentials and Qualifications

Bachelor’s degree in Medical Technology or a related Biological Science. Demonstrated competency in diverse biological processes with adherence to good documentation practices. Ability to work independently to meet established goals, expected outcomes and deliverables. One (1) – two (2) years clinical laboratory experience or previous cell processing / cell therapy experience or successful completing of Cell Therapy Technologist trainee requirements. Relevant experience includes, but are not limited to, cell culture experience, blood or blood product processing, or immune quality control assay experience (flow cytomertyr cytometry, qPCR, ELISA, endotoxin testing). 20/20 near vision (corrected or uncorrected)