NL-RD

Test and Verification Engineer.,Job Description Philips is a global leader in health technology, committed to improving billions of lives worldwide and striving to make the world healthier and more sustainable through innovation. Driven by the vision of a better tomorrow. But its not just what we do, its who we are. We are 70,000, wonderfully unique individuals, with two things in common. An unwavering sense of purpose and a relentless determination to deliver on our customers needs. Its what inspires us to create meaningful solutions the kind that make a real difference when it matters most. The world and our customers needs are changing faster than ever before and while we are proud of what we do already, we know we can do more. Thats why we need you, to help us tackle increasingly complex challenges posed by ever evolving health and well-being needs. In this role, you have the opportunity to Be part of a multidisciplinary team of highly skilled technical specialists working on innovative (automated) test solution projects. These projects can cover every phase of the product life cycle, from development (requirements engineering, development and validation of new test methods, test strategy development, definition and execution of test protocols), manufacturing (manufacturing test development, fitness for use, MSAs) and maintenance (development remote monitoring solutions, predictive maintenance solutions, test system health checks, crash support). In your role, you will work with together with (sr.) Test architects, the SW architects (automation) and other T&V Engineers from within our own organization as well as from our customers organization. You are responsible for Creating, reviewing and optimizing test designs, reusable test protocols, and test procedures to ensure complete functional and non-functional test coverage for multiple project and/or products concurrently. Developing and conducting tests to verify functionality (performance, reliability, security, compliance,…) based on a risk-based strategy, against the design input requirements and formally reporting the results. Documenting test plans, protocols, and reports. Reviewing product requirements, designs and product changes from a test point of view and liaising with stakeholders resulting in a testable and maintainable systems and converting requirements into test specifications and tester designs. You are a part of The Test and Verification Engineering team which is part of the Quality & Reliability Engineering department of Philips Innovation Engineering and is a diverse group of more than 28 technical experts located in Eindhoven (NL), Pune (In) and Boston (US). All have extensive experience in the field of test and verification strategy definition, requirement engineering and/or test automation and are actively supporting complex, innovative projects for our customers (all Philips businesses) located all over the world. To succeed in this role, we are looking for a Test Engineer with following characteristics: Masters (MSc) degree in Physics, Electrical Engineering, Mechanical or Industrial Engineering. At least 3-5 years of relevant experience in professional engineering. Experience of working in a highly regulated environment, preferable in medical device industry Professional with experience in Design Verification and Product verification. Experienced with Good Documentation Practices Guides the selection of the most effective test design techniques. Defines acceptance tests for verification of requirements with shared responsibility for project scope, requirements and risks. Has ownership of test design, reusable test protocols and test procedures to ensure complete functional and non-functional test coverage. Has ownership of planning and timely execution. Someone with a hands-on mentality. Stakeholder management within and beyond own team, e.g. functional managers, project manager, test architects, systems architects, development engineers, external test labs, customers.
Able to creates a test plan for a part/element Very good experience in testing and verification process Experience in the execution of Measurement System Analyses (MSAs) Relevant project experience in ISO13485 Medical Device directive is a plus Motivated, self-driven with a determination to succeed and ability to adapt to change Analytical, structured and open to new ideas Open to travel on an occasional basis, .