Rhys Davies
About Rhys Davies
Rhys Davies is a QA Associate specializing in Computer System Validation at MeiraGTx, where he co-leads the Data Governance program. He has a strong educational background in biochemistry and molecular oncology, and extensive experience in quality management across various organizations.
Work at MeiraGTx
Rhys Davies currently holds the position of QA Associate, CSV at MeiraGTx, where he has worked since 2019. In this role, he co-leads the Data Governance program, focusing on the implementation and validation of systems for clinical trials, manufacturing, quality control, and engineering. He is responsible for delivering company-wide training on the Quality Management System and authors and manages quality technical agreements. His work supports the development and implementation of electronic Quality Management Systems across the organization.
Previous Experience in Quality Assurance
Before joining MeiraGTx, Rhys Davies worked as a QA Associate at Seqirus from 2015 to 2017 in Liverpool, United Kingdom. He then served as a Quality Specialist at Clinigen Group from 2017 to 2019 in London, United Kingdom. In these roles, he gained experience in liaising with GMP and GCP business functions and managing client audits related to Quality Management Systems and Pharmacovigilance.
Education and Expertise
Rhys Davies has a solid educational background in the sciences. He studied at Bro Myrddin Welsh Comprehensive School, achieving 11 A*-C GCSEs, and completed A levels in Mathematics, Biology, and Chemistry from 2006 to 2008. He earned a BSc (Hons) in Biochemistry from The University of Liverpool between 2009 and 2012, followed by a Master of Research (MRes) in Molecular Oncology from 2012 to 2013.
Skills in Quality Management Systems
Rhys Davies specializes in liaising with GMP and GCP business functions to implement and validate systems essential for clinical trials and manufacturing processes. His expertise includes managing and hosting client audits related to Quality Management Systems and Pharmacovigilance. He plays a key role in ensuring compliance and quality standards within the organization.