Job Description

Job Title Systems EngineerSystems Engineer:You will be a part of the Engineering group that is responsible for implementing technical strategies, evaluating, and developing products, and providing a superior level of technical support that benefits the organization. The Systems Engineer: Lead collaborates closely with Engineers, Architects, and Test in the Ventilation business within Sleep and Respiratory Care to develop and commercialize Class 2 medical devices.You will be involved in all system engineering aspects of the Philips V-model, starting with conceptualization, writing requirements, functional and technical design, check & optimize, verification, integration and finally the validation. In your role, you will support system architects and engineers to integrally manage all system engineering aspects in a model-based way supported by the appropriate tools. You will maintain and develop knowledge and expertise resulting in state-of-the-art approaches to serving our customers.Your role:Incorporates essential operating mechanisms of systems engineering of medical device design and engineering principles and adheres to medical device regulations.Defines User Requirements, system requirements, FMEA, architecture, and interfaces to meet product requirements, risk analysis and industry standards; conducts system design analysis to select key components and defines control methods; and coordinates build and design integrationWorks together to support product verification and validation planning, resolution of technical integration issues, safety agency interface, system testing and coordination and interfaces with Philips design center.Conducts design reviews as part of the product development process to ensure customer requirements are met and the designs are manufacture-able, serviceable, and reliable. In addition, it does the same for subsystem requirements and product integration.As a System Engineering Expert, you will:Lead and Support the development of System engineering content in R&D (Research and Development) projects across the business.Manage the system engineering information and its traceability (requirements, risks, design decisions, protocols, results) in the model-based system environment of the businessCreate adequate requirements and designs for solutions, products, services, and testersDeploy best system engineering practices globally in Philips to R&D project teams or organizations via training & coaching to enhance maturityIdentify improvement opportunities in Philips businesses proposition and develop actionable proposals, plans and tailored training materials or workshops to address theseManage your activities and services according to good project management practicesCoordinate small teams of system engineers if applicableYou\'re the right fit if:Bachelors, MS or PhD in a relevant field including Electrical, Mechanical Engineering, or other related science.8 to 20 years of experience successfully developing complex medical device (hardware, software, consumables) products for acute care/hospital markets is necessary.Additional technical knowledge and hands-on experience in ventilation will be added advantage.Defines User Requirements, system requirements, FMEA, architecture, and interfaces to meet product requirements, risk analysis and industry standards; conducts system design analysis to select key components and defines control methods; and coordinates build and design integrationExperience with Sustenance Engineering, Change review Board, Defect ManagementExperience with conducting cross-discipline feasibility and trade off studies to evaluate electronic, mechanical, and pneumatic performance from subsystem to system level for issue resolutionsAnalytical and architectural thinking, system view, physical insight, flexibility, and a hands-on mentality to deliver sustainable results and creative solutions.Strong understanding of System Design process including Model-based Design approach and Test-Driven design methodologiesReview System Verification and Validation plan/protocols, Test Method Validation (TMV)Conducting Technical Review & Decision MakingUnderstanding of global medical device regulatory environments and clearance processes.Effective communication, computer, documentation, presentation, and interpersonal skills are required, as well as the ability to work both independently and as part of a team.Maintains strict confidentiality of sensitive information.About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won\'t stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.

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If you\xe2\x80\x99re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion .#LI-PHILIN

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