Certified Lead Auditor EN ISO 13485:2016 ( Quality Management Systems for Medical Device Manufacturers)
2016 - 2016
University of Applied Sciences in Hamburg
Master of Science ( Biomedical Engineering)
2008 - 2009
University of Applied Sciences in Hamburg
Bachelor of Science ( Biomedical Engineering)
2002 - 2008
Christian Teaching Institute
Baccalaureate ( Philosophy)
1986 - 1999
Lead Auditor Training
M.Sc Georges Hakim's Skills
TÜV Süd Certified Regulatory Affairs Manager
TÜV Süd Certified Technical Documentation Specialist
TÜV Süd Certified Quality Management System Specialist
Regulatory Affairs
Project Management
Technical Documentation
Conformity Assessment
Medical Devices
ISO 14971
ISO 13485
M.Sc Georges Hakim's Summary
m.sc Georges Hakim, based in St. Gallen, Saint Gallen, Switzerland, is currently a Director Global Quality Assurance and Regulatory Affairs at Leica Microsystems, bringing experience from previous roles at Medela, Inc.. m.sc Georges Hakim holds a 2016 - 2016 Certified Lead Auditor EN ISO 13485:2016 in Quality Management Systems for Medical Device Manufacturers @ BSI Training Academy. With a robust skill set that includes TÜV Süd Certified Regulatory Affairs Manager, TÜV Süd Certified Technical Documentation Specialist, TÜV Süd Certified Quality Management System Specialist, Regulatory Affairs, Project Management and more, m.sc Georges Hakim contributes valuable insights to the industry. m.sc Georges Hakim has 2 emails on RocketReach.