Didier Hallard
About Didier Hallard
Didier Hallard serves as the Director Qualified Person at Kite Pharma, Inc. in Santa Monica, California, a position he has held since 2019, bringing extensive experience from previous roles in quality assurance across various companies in the Netherlands and the United States.
Work at Kite Pharma
Didier Hallard serves as the Director Qualified Person at Kite Pharma, Inc. since 2019. In this role, he is responsible for ensuring compliance with regulatory requirements and overseeing quality assurance processes. His tenure at Kite Pharma is marked by a commitment to maintaining high standards in pharmaceutical manufacturing and product quality. The company is located in Santa Monica, California, where Hallard contributes to the development and commercialization of innovative cancer therapies.
Previous Experience in Quality Assurance
Before joining Kite Pharma, Didier Hallard held several positions in quality assurance across various organizations. He worked as a Senior Consultant - Qualified Person at Xendo from 2016 to 2018. Prior to that, he served as Associate Director QA CMO and Qualified Person at Biomarin Nederland B.V. for one year. His earlier roles at Biomarin included Director QA and Qualified Person from 2009 to 2015, where he focused on quality management systems and compliance.
Education and Expertise
Didier Hallard has an extensive educational background in pharmacy and quality assurance. He earned his Doctor of Pharmacy degree from Université De Tours, completing his studies from 1987 to 2004. Additionally, he obtained a Doctor of Philosophy from Leiden University, studying from 1996 to 2000. His academic qualifications provide a strong foundation for his expertise in pharmaceutical quality assurance and regulatory compliance.
Career Progression in the Pharmaceutical Industry
Didier Hallard's career in the pharmaceutical industry spans over two decades, with a focus on quality assurance roles. He began his career at Eurofins Central Laboratory as a Study Coordinator and QC Manager from 2000 to 2002. He then progressed through various positions at Octoplus, including Manager Quality Assurance and Supervisor Qualified Person. His experience in these roles has equipped him with a comprehensive understanding of quality systems and regulatory requirements in the pharmaceutical sector.