Director Of Quality Management, Risk & Compliance
Leuven
Our diversified activities include industrial additive manufacturing including aerospace production, AM Software, patient-specific medical devices and medical device software, and consumer products. Responsible, as management representative, for corporate Quality Management and Regulatory Affairs, reporting to the CEO. Also active within our ISO 14001 EMS.Since 2019, we have expanded the scope of our team activities in the direction of risk management, including Information Security, as well as general compliance.I am also leading the company's initiatives with respect to CSR.Achievements include setting up and working with our teams to implement our MDD-to-MDR transition strategy, including CE-marking of medical devices. As a team, we take pride in our excellent external audit track record and continuous certification (ISO 9001, ISO 13485, MDSAP, EN9100)