Industrialization // DFMAT (Design For Manufacturing Assembly and Testing) // Process Validation // Equipment Qualification // manufacturing transfers // NPI (New Product Introduction) // Medical Devices- Design, implement and validate manufacturing processes, tools and equipment for quality, efficiency and costs and release/handover towards factory- Securing factory Manufacturing and Supply Chain Requirements / Design Rules and defining and implementing standards at R&D (based on DFMAT principles)- Review and approval of product designs created by R&D- Global (dual) manufacturing transfers and ramp up (applying lean principles)- Process Validation and Equipment/Tool Validation to assure consistent produced medical devices in NPI projects;... Following V-model based PDLM (Product Development Launch and Maintenance) milestone process... Applying PFMEA, PMAP (process flow), PVP, EQ, IQ, TMV, OQ, PQ and PPQ... Complying to safety and regulatory requirements- Responsible for release of M-BOM and production routing Master data- Preparation, review and release of manufacturing documentation (SOP) like Work Instructions and Device History Records (DHR) as per factory Quality Management System (QMS)- Assuring product design (DMR, configuration and BOM) and supply chain to enable Make2Stock, late customization and configuration bundling- Bridging between GME (Philips Global Manufacturing Engineering) - PI (Product Industrialization) - BU (Business Unit) on strategic manufacturing and testing aspects- Recruiting, interviewing and onboarding new team membersDXR - Diagnostic X-Ray @ Philips Healthcare (Medical Systems)

NPI (New Product Introduction) // industrialization // DfX // mechanics // complex High-Tech assembly (Semicon systems)- Technical and quality responsible for sub-systems (Building Blocks) and full system assembly, in collaboration with supplier, semicon customer, development teams and production- Definition (based on DfX, pFMEA), release and secure (Control Plans, SPC, Qualification Reports, Work Instructions) of assembly and qualification processes and production flows- Transfer production and qualification processes to production in cleanroom (Proto / Release for Volume / Pilot phase)- Organizing and participating in review sessions for Engineering Changes (internally @ VDL and externally with TPD owner) and transfer to stakeholders (supplier, logistics, supply chain, factory engineering, production)- Problem solving in pilot phase (8D)- Coordinating/monitoring issue resolution, component/assembly deviations and product qualifications

NPI (New Product Introduction) // assembly // industrialization // process development and improvements // medical X-ray detectors- Development of assembly processes and mechanical tools for X-ray detectors and sub-assembly and release; manufacturability (DfA), risk analysis (pFMEA, process windows), upscaling, efficiency, ISO 9001/13485- Definition of assembly processes, production flows, routings and production floor (cleanroom class 100, ISO 5)- Definition, maintenance and applying of design rules- Transfer of assembly, control and testing processes to production; capability runs, training of operators and assembly engineers- Definition (requirements), purchase, acceptance and release of production equipment and mechanical tools (FAT/SAT)- Definition and introduction of process and equipment prescriptions and control plans (OCAP)- Initiate improvement projects, executing and implementing (yield improvements, cost down)

Process development // immuno assays // medical devices // bio chemistry- Improve, upscaling and transferring to manufacturing of production processes for production of disposable cartridges and specification of new processes (including bio materials)- Execution of verification of developed processes and documentation according product creation and quality system- Definition of requirements for production equipment, acceptance and release (FAT/SAT)- Leading team of Process Development Engineers

Quality // Reliability // electronics // physics // optics // chemistry- Link between R&D - Process Development - System Engineering- Definition of test roadmaps (reliability, test strategies)- Definition, execution and implementation of release and test procedures for materials and developments (e.g. electrical driving and material developments)- Execution & analysis of (reliability) tests, including failure analysis- Definition, purchase and release of test setups; tooling, equipment, automation, climate chambers- Daily leading T&C team of 8 engineers/technicians (academic, bachelor, intermediate vocational)- Growing team capacity (from 2 up to 8 persons) and capabilitiesDevelopment Engineer:- Definition, execution and reporting of feasibility studies (project lead); e.g. footprint reduction, spacering, oil motion control- Definition and realization of measurement/test setups- Process and material innovation, release and introduction in pilot and production line

Chemistry ◾ optics ◾ physics ◾ electronics◽ Detection and filtering of hazardous nano-particles in exhaust fumes◽ Manipulation of direction of light via anisometric plate-like particles by electrical field (Smart Light Management)◽ High reflective, high temperature resistant coatings for lighting applications