As of May 1st, 2019 I became Head of Quality for Philips Research and responsible for the quality of Research services through continuous improvement and deployment the Philips Research Quality Management System.The Research QMS spans 7 laboratories around the globe (Eindhoven, Hamburg, Paris, Cambridge (US), Bangalore, Shanghai and Skolkovo (RUS).

Risk management trainer and facilitator. Quality management.

Managing QMS changes, CAPA Coordinator, Document & Record Control process owner, Training Manager, ...Quality Engineer for SW Development projects.

Supporting the SW projects to comply with the applicable QMS (CDP2 or Customer QMS) and applicable legislation / regulation / standards: - Create quality plans for projects- Help apply QMS processes and WoW's- Support in applying requirements of relevant standards- Create Product risk management plans and V&V plans- Monitor Requirements traceability upon completion- Assist in experimental setups (compliance to relevant standards, like ISO14155)- Prepare milestone reviews by collecting the status of all deliverables- Ensure proper approval of deliverables- Facilitate risk assessments and provide training- Participate in review meetings- Review and approve Corrective Actions and Preventive Actions (CAPA)- Review and approve Product change controls for Quality & Regulatory compliance impact and determine requirements for implementationAssure Quality & Regulatory compliance of project activities and output.Help create a Quality Management system for Connected Digital Platform & Propositions.

Advise venture managers and BPO's in the biomedical domain on quality & regulatory issues, like setting op clinical trials, CE-marking, vigilance reporting, etc.Setting up and maintaining ISO13485 quality management systems for Lab. ventures. Planning and executing audits. Document sales & contracting processes of Philips Research Europe - Eindhoven, and make them compatible with Philips'​ Internal Control Standards and Sarbaines-Oxley (SOx) regulations.Setting-up and maintaining our group's PBE management system.

Supporting the SW projects to comply with the applicable QMS (PInS or Customer QMS) and applicable legislation / regulation / standards: - Create quality plans for projects- Help apply QMS processes and WoW's- Support in applying requirements of relevant standards- Create Product risk management plans and V&V plans- Monitor Requirements traceability upon completion- Assist in experimental setups (compliance to relevant standards, like ISO14155)- Prepare milestone reviews by collecting the status of all deliverables- Ensure proper approval of deliverables- Facilitate risk assessments and provide training- Participate in review meetings- Review and approve Corrective Actions and Preventive Actions (CAPA)- Review and approve Product change controls for Quality & Regulatory compliance impact and determine requirements for implementationAssure Quality & Regulatory compliance of project activities and output.Help create a Quality Management system for PInS Software.

Writing technical documentation for, machinery, software, etc.