Emma Lester is a Quality Management and Regulatory Affairs professional with over 15 years of experience in the medical device and laboratory developed tests sectors. Currently serving as the Director of Quality & Regulatory Affairs at Cleo Diagnostics, Emma specializes in implementing and maintaining quality management systems in compliance with industry regulations. Their prior roles include Quality Manager at Genetic Technologies Limited and Head of Quality at Incisive Technologies, where they successfully led numerous regulatory projects and built high-performing quality teams. Emma holds a Bachelor of Forensic Science and a Master of Science in Biotechnology, complementing their extensive expertise in regulatory affairs with a solid educational foundation.
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