James Guidry Ii
About James Guidry Ii
James Guidry II is a Cell Therapy Specialist II at Kite Pharma, Inc., with extensive experience in pharmaceutical manufacturing and quality assurance. He has worked with several industry leaders and holds a Bachelor of Science in Biology and an MBA in Healthcare Administration.
Work at Kite Pharma
Currently, James Guidry II serves as a Cell Therapy Specialist II at Kite Pharma, Inc., a role he has held since 2016. His responsibilities include overseeing cell therapy processes and ensuring compliance with industry standards. He has been instrumental in maintaining high professional standards and has demonstrated strong attention to detail in his work. Kite Pharma focuses on innovative cancer therapies, and Guidry's expertise contributes to the company's mission in the biopharmaceutical sector.
Previous Experience in Pharmaceutical Manufacturing
James Guidry II has extensive experience in pharmaceutical manufacturing and quality assurance. He worked at Caladrius Biosciences as a Clinical Manufacturing/Immunotherapy specialist from 2014 to 2016. Prior to that, he was employed at Bbraun Medical as QC Process Control III from 2014 to 2015. His career also includes a position as a Senior Manufacturing Associate at Dendreon from 2010 to 2014 and as a Senior Associate at Amgen from 2006 to 2007. This diverse background has equipped him with a strong understanding of good laboratory practices and compliance.
Education and Expertise
James Guidry II holds a Bachelor of Science in Biology from Xavier University of Louisiana, which he completed from 1996 to 2001. He furthered his education by obtaining an MBA with a concentration in Healthcare Administration from the University of Phoenix between 2011 and 2012. Additionally, he studied Sterile Processing Technology/Technician at Martinson College, earning a certificate from 2015 to 2016. His educational background supports his expertise in laboratory practices and healthcare administration.
Skills in Quality Assurance and Laboratory Practices
Guidry possesses a strong understanding of good laboratory practices (GLP), good manufacturing practices (cGMP), and good documentation practices (GDP). He utilizes Laboratory Information Management Systems (LIMS) and instrumentation to collect, record, and analyze data effectively. His approach to challenges emphasizes creativity and innovation while ensuring compliance with lab protocols, which is essential in the highly regulated pharmaceutical industry.
Recognition and Professional Standards
James Guidry II has been recognized for his exemplary performance in various roles throughout his career. His strong attention to detail and commitment to maintaining high professional standards have contributed to his success in the pharmaceutical manufacturing sector. His work has involved collaboration with industry leaders, enhancing his reputation as a reliable professional in quality assurance and cell therapy.