As Quality Manager I am investing me a lot to get our ISO 9001 certification renewed and to get an ISO 13485 certification for medical equipments later on. The company's products are addressing both the research and the patients.
I am also handling organization functional restructuring to improve the information flux leading to better decision-making.
This implication requires to connect existing IT system like MRP, PLM, CAD and SAGE by rationalizing the exchanged data and the processes.
I am also member of several forums focusing on the medical devices international regulations and thus be looked as legal council for the company about all the MD regulatory aspects.
Mes compétences :
Commercial
Développement commercial
Ingénierie
Management