Mark Asquith

Mark Asquith is currently the Validation Manager at QIAGEN, where they oversee project planning and the generation of validation documentation. Previously, Mark worked as a Validation Specialist at Validation in Partnership, managing validation documentation and execution across various equipment and environments. They also held a contract position as a Validation Specialist at Lonza Biotechnology Ltd. and served as a Steriliser Support Officer at AstraZeneca Pharmaceuticals, focusing on the qualification of autoclaves for aseptic manufacturing. Mark has extensive experience in validation processes and has contributed to successful customer and FDA audits.