Peter Fransen Email & Phone Number

Eindhoven, Nb, Nl

Eindhoven, Noord-Brabant, Nederland

Eindhoven Area, Netherlands

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).

High Tech Campus 34, Room 5.038, 5656Ae Eindhoven

Risk management trainer and facilitator. Quality management.

High Tech Campus 34, Room 4.038, 5656Ae Eindhoven

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

Eindhoven Area, Netherlands

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.

Eindhoven Area, Netherlands

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.