Mark Lund-Conlon is a Validation and Computer System Validation (CSV) Specialist with extensive experience in regulatory compliance for IT implementations in the pharmaceutical sector. They served as a Director and Senior Consultant at Mouse Matters Limited from 2011 to 2019, advising clients on SAP and Pharmaceutical CSV projects globally. Mark has held roles such as SAP EWM Implementation Project Test Manager at United Drug and GxP Validation & Compliance Specialist at Smith & Nephew, showcasing expertise in managing complex testing, validation activities, and compliance audits. Currently, they are a CSV Specialist at the CPI Medicines Manufacturing Innovation Centre, focusing on enhancing medicine manufacturing processes while ensuring regulatory compliance. Mark holds a BEd (Hons) in Education & English and an MA in Literature.
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