Regulatory and Quality Affairs Manager, Adele Simms, has 20+ years’ experience in biotech, medical devices and in vitro diagnostic with roles from Production Scientist to Compliance Manager, Quality Director, Regulatory Affairs Specialist, and as an independent QMS and Medical Directives Auditor working on behalf of LRQA and BSi. She has a BSc and MSc in Biological Sciences from the University of Essex, and a HNC in Business and Finance.
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