Moffitt Cancer Center

Opportunity to join a NCI designated comprehensive cancer center involved in the development of novel cellular therapy treatments for cancer patients. Working knowledge of Adoptive Cell Therapy. Robust communicator, engaged, and will work closely with members of the Cell Therapy Team.. Comply with the facility's standard operating procedures and policies which incorporate the cGMP/cGTP, FACT, and CAP regulatory standards applicable to cellular therapy product production and analysis.. Bachelor's Degree in a laboratory science in biotechnology, medical technology, biology, chemistry, or biochemistry

technical writer

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 Position Highlights: <ul><li> Opportunity to join a NCI designated comprehensive cancer center involved in the development of novel cellular therapy treatments for cancer patients </li><li> Responsible for supporting Cell Therapies management with client project producing high-quality cGMP and processes documentation. </li><li> Initiating and preparing batch records as well as preparing material and product specifications based on project requirements </li></ul> The Ideal Candidate <ul><li> Strong detailed knowledge of cGMP manufacturing environment </li><li> Working knowledge of Adoptive Cell Therapy </li><li> Understanding of good documentation practices and requirements </li><li> Robust communicator, engaged, and will work closely with members of the Cell Therapy Team. </li><li> Exhibit interest and excitement in participating in the advancement of cellular products </li><li> Advanced skills in MS Office and Excel </li></ul>Responsibilities <ul><li> Work closely with technical development team to establish documents and reports and maintain throughout the development lifecycle. </li><li> Manage and escalate timing issues related to documentation including authoring, review, and approval. </li><li> Comply with the facility's standard operating procedures and policies which incorporate the cGMP/cGTP, FACT, and CAP regulatory standards applicable to cellular therapy product production and analysis. </li><li> Interpret, follow, and communicate regulatory guidelines and apply knowledge to documents as applicable. </li><li> Create and maintain standard templates and modules. </li><li> Other duties as assigned. </li></ul>Credentials And Qualifications <ul><li> Bachelor's Degree in a laboratory science in biotechnology, medical technology, biology, chemistry, or biochemistry </li><li> Minimum of 2 years of experience in laboratory operations. </li><li> Strong detailed knowledge of cGMP manufacturing environment </li><li> Demonstrated ability to work independently to achieve expected outcomes</li></ul>

START NEW SEARCH