Daniel Mannion
Head of Global Compliance
Masters in Molecular and Cellular Biochemistry (Oxford). Medical Device Compliance Quality Assurance Specialist (CE Marking, FDA (510(k))
Masters in Molecular and Cellular Biochemistry (Oxford). Medical Device Compliance Quality Assurance Specialist (CE Marking, FDA (510(k)), ISO 13485 Lead Auditor, 6 Sigma Green Belt, Dipl. Leadership and Management. Several years of experience as a Quality Engineer with global high-tech electronic medical device companies. Has also implemented and worked on IATF 1694, ISO 9001, ISO 14001, TS16949 and AS9100 quality standards and VDA 6,3 process audits. NEBOSH General Certificate.