Aimee Lam
About Aimee Lam
Aimee Lam is a QA Specialist in IT and CSV at MeiraGTx, with a background in quality assurance roles across various organizations in the UK. She holds a BSc (Hons) in Biomedical Science from the University of Surrey and has extensive knowledge of regulatory guidelines and risk-based strategies.
Current Role at MeiraGTx
Aimee Lam currently serves as a QA Specialist, IT & CSV at MeiraGTx, where she has been employed since 2018. In this role, she focuses on quality assurance processes related to computerized systems and data integrity. Her responsibilities include developing risk-based strategies for validation and ensuring compliance with industry regulations.
Previous Experience at MeiraGTx
Prior to her current position, Aimee worked at MeiraGTx as a QA Documentation Controller from 2017 to 2018. During this time, she contributed to the management of quality assurance documentation and processes, ensuring adherence to regulatory standards within the organization.
Career Background in Quality Assurance
Aimee has a diverse background in quality assurance roles across various organizations. She worked as a Quality Assurance Administrator at Retroscreen Virology Group plc from 2014 to 2015. Additionally, she held the position of Quality Assurance Associate at Norgine from 2015 to 2017, where she continued to develop her expertise in quality management.
Educational Qualifications
Aimee Lam earned a Bachelor of Science with Honours in Biomedical Science from the University of Surrey, completing her studies from 2009 to 2013. Prior to this, she attended Palmers College, where she studied Mathematics, Biology, and Chemistry at the A Level, and Hassenbrook Specialist Technology College, where she achieved 14 GCSEs including English, Mathematics, and Science.
Regulatory Knowledge and Skills
Aimee possesses extensive knowledge of key regulatory frameworks, including EU Annex 11, 21 CFR 11, ISPE GAMP5, ISPE Data Integrity, and ICH Q9. She is experienced in implementing and managing computerized systems throughout their lifecycle, which includes validation, SOP authoring, training, change management, and incident management.