Mhairi Coyle

Mhairi Coyle, PhD, currently serves as a Clinical Submissions Specialist at QIAGEN, focusing on IVDR submissions for companion diagnostic trials. Previously, Mhairi held the position of Senior Project Manager in QA/RA at Abbott, managing critical regulatory projects, including compliance transitions for IVDR and MDR regulations. Mhairi has also worked as a Project Manager at Symbiosis Pharmaceutical Services Limited, coordinating internal projects such as FDA audit preparations, and contributed to external collaborations as a Lead Product Development Scientist at Quotient Limited. Early career experience includes roles as a Protein Scientist at Piramal Healthcare UK and as a Downstream MS&T Lab Representative at Eli Lilly and Company, emphasizing project management and technical transfer in biotech processes. Mhairi holds a PhD in Bio-Organic, Bio-Analytical and Protein Chemistry from the University of Strathclyde and a BSc (Hons) in Chemistry, IT and Instrumentation from Glasgow Caledonian University.