Hakim M.

Hakim M. has extensive experience in the medical device industry, working at GMED since September 2010. Hakim holds various titles including Responsable organisme de formation, Responsable de la planification et des ressources externes, and Certification project leader. Hakim is responsible for managing medical device certification and auditing the company for compliance with ISO13485, ISO9001, and MDD 93/42/CE standards. Prior to GMED, Hakim worked at Resmed as a Product Quality Engineer from September 2005 to August 2010, where Hakim managed non-conformity goods from suppliers and led projects to improve production lines. Hakim graduated from the University of Technology Compiègne in 2005.