Adele Simms - Quality & Regulatory Affairs Manager
Adele has over 20 years’ experience in biotech, medical devices and in vitro diagnostics. She has had senior roles across Production, Quality Control, Quality Assurance and Regulatory Affairs at several life science companies such as Lonza Biologics, Wellcome (GSK), Genzyme, Chemicon (Merck) and Scapa Healthcare, specialising in monoclonal antibodies and hydrogel technology. She has also worked as a IRCA certified QMS and Medical Directives Lead Auditor for over 10 years assessing quality systems and technical documentation on behalf of LRQA and BSI. She holds a BSc and MSc in Biological Sciences from the University of Essex, and a HNC in Business and Finance.