Alexander John Hallam
About Alexander John Hallam
Alexander John Hallam is a QA Manager with extensive experience in microbiology and quality assurance. He has held various positions in the pharmaceutical and biotechnology sectors, including roles at Sanofi and Instil Bio, and has a strong background in laboratory management and training.
Current Role as QA Manager
Alexander John Hallam currently holds the position of QA Manager at Instil Bio, where he has been employed since 2021. His role involves overseeing quality assurance processes and ensuring compliance with regulatory standards. He is based in the Manchester Area, United Kingdom, and has been instrumental in leading quality initiatives within the organization.
Previous Experience at Instil Bio
Prior to his current role, Hallam worked at Instil Bio as an Associate QA Manager for three months in 2020. He also served as a Senior QA Scientist at the same company for ten months in 2020. His tenure at Instil Bio has provided him with valuable experience in quality assurance and regulatory compliance within the biopharmaceutical sector.
Background in Microbiology
Hallam has a solid background in microbiology, having worked as a Microbiologist at Sanofi from 2015 to 2017. He also served as a Microbiology Technician at Eurofins Agroscience Services for two months in 2014. His experience in microbiology has equipped him with extensive knowledge in method validation, equipment qualification, and environmental monitoring.
Education and Qualifications
Hallam earned his Master's Degree from the University of Birmingham in 2014, following a Bachelor's Degree from Lancaster University in 2013. His academic background supports his professional expertise in quality assurance and microbiology. Additionally, he is qualified as a First Aider, Health and Safety officer, and Fire Warden, highlighting his commitment to workplace safety.
Training and Development Initiatives
In his professional capacity, Hallam has designed GMP training programs aimed at enhancing colleagues' skills in cleanroom activities. This initiative reflects his focus on facilitating the transition of research projects to Good Manufacturing Practice (GMP) standards, contributing to the overall quality and safety of laboratory operations.