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Design, review, and optimize test designs, reusable test protocols, and test procedures to ensure comprehensive functional and non-functional test coverage across multiple projects and products
Develop and execute tests to verify performance, reliability, security, and compliance based on a risk-based strategy
Document test plans, protocols, and reports while ensuring adherence to regulatory requirements
Analyze product requirements and design changes from a testing perspective, converting them into test specifications and system validations
Work closely with internal and external stakeholders, including functional managers, project managers, test architects, system architects, development engineers, and external test laboratories.
Requirements:
Master’s (MSc) degree in Physics, Electrical Engineering, Mechanical Engineering, or Industrial Engineering
3-5 years of relevant professional engineering experience
Experience working in a highly regulated environment, preferably in the medical device industry
Strong background in Design Verification and Product Verification
Proficiency in Good Documentation Practices
Expertise in selecting effective test design techniques and defining acceptance tests for verification
Ownership of test design, reusable test protocols, and execution planning
Hands-on approach with a proactive mindset
Strong stakeholder management skills across different teams and external partners
Experience in Measurement System Analyses (MSAs)
Familiarity with ISO13485 Medical Device Directive
Analytical and structured thinker, adaptable to change, and open to new ideas
Willingness to travel occasionally.
Nice to have:
Familiarity with ISO13485 Medical Device Directive
What we offer:
Opportunity to work in a multidisciplinary team of technical specialists
Collaboration with senior test architects, software automation architects, and other engineers
Exposure to innovative projects across Philips businesses worldwide
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