דרושים Electronics Engineer - Lcm Philips Best ב-Philips ב-הולנד

Start date: November 1st, 2025

Duration: 5-6 months (with possibility to extend)

Type:Internship, (thesis possible)

Weekly presence:32-40 hours

Job title:

Internship: Software Development Engineer / Website Developer

Your role:

• Develop a responsive and visually appealing website using modern frameworks

• Implement an interactive cost calculator that allows users to input expected service usage information and get instant costs based on price list

• Ensure the website is optimized for performance

• Integrate back-end logic for data processing and storage

• Develop unit, component and system tests to assure proper quality and conformance with requirements

You're the right fit if:

• You are studying towards a BSc (last year) or MSc insoftware engineering/computer science.

• You are interested in cloud development such as AWS

• Basic to intermediate knowledge of modern web development (front-end and back-end)

• Some experience with building websites(academic, internship or professional)

• Ability to work independently and deliver within agreed timelines

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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You will be responsible for maintaining, validating, and verifying complex mechanical components and subsystems, ensuring our advanced medical imaging solutions remain safe, reliable, and compliant with international standards throughout their lifecycle.

• As Senior Mechanical Designer (LCM), you will safeguard the quality, reliability, and patient safety of Philips’ medical imaging systems—supporting clinicians to deliver precise and effective patient care across the globe.

• You will be part of the Engineering Department within the Lifecycle Management (LCM) Mechatronic Development Cluster, part of the IGT Fixed Systems R&D organization. This diverse and collaborative team works on both lifecycle management and new product introductions (PDLM). You will collaborate with colleagues across disciplines (electrical, electronics, mechatronics, compliance, validation, purchasing, and quality) as well as external suppliers and partners.

• This position offers the chance to deepen your expertise in lifecycle management, regulated product development, and cross-disciplinary collaboration. You’ll strengthen your skills in mechanical design, analysis, testing, and verification

• 10+ years in professional engineering, including at least 5 years in mechanical development, testing, or measurement in a highly regulated industry (medical preferred).

• Strong expertise in mechanical design & analysis, lifecycle management, testing, verification, and automation. Hands-on, accurate, and improvement-driven.

• Master of Science in Mechanical Engineering or a related technical discipline.

• Excellent communicator and team player, proactive, energetic, and experienced in cross-functional collaboration. Familiarity with SAFe is a plus.

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’re 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 culture of impact with care .

A strong local stocking plan is a strategic requirement for Service Delivery and as the Regional Service Parts Planner you will drive this plan.

You are responsible for:

• Partnering with colleagues within the SPS regional team, SPS Strategic planning, Business, Markets, SPS Supply management, SPS Master data, SPS ASAP desk, and other disciplines to secure parts availability in your region
• Managing the Planning Process: demand forecasting and stock target setting in your regional locations
• Utilizing the advanced planning tool to periodically validate and update the parts planning, follow-up on planning alerts, and master data management
• Analyzing Stock-outs and Material Availability misses, in order to create and execute on corrective actions and preventive action plans
• Represent SPS Planning in the SPS regional team to ensure impact on service parts are considered and to execute on plan
• Being a contact person in case of escalation regions on customer service level requirements
• Manage overall inventory in your region, including inventory on shelf and aligning with market team son on market managed inventory
• Participate in projects as needed, contributing to structural improvements on SPS priorities

To succeed in this role, you’ll need a customer-first attitude and the following :

• Master or Bachelor’s Degree with Supply Chain Planning and/or Supply Chain operations,
• At least 5-8 years of working experience in Supply Chain operations, preferably at large company in an international environment,
• Fluency in English
• Strong analytical capabilities, clear communicator, standout colleague,
• Detail oriented and able to make clear decisions with available information
• Experience in working with a Supply Chain Planning tool, SPM preferred
• An excellent understanding of SAP ERP Systems and Data
• Experience within Customer Service and Healthcare industry is preferred
• Creativeness, thinking in solutions and driving implementation
• Experience with LEAN deployment is preferred

Your role:

• You make a substantial contribution to the innovation of our clinical products. You help in engineering advanced 3D clinical applications.
• You oversee and implement the hyper-automation-based software build, test and deployment for our present and future interventional Applications (iApps).
• You define best practices including the test and integration strategy and policies for software deployment, evaluate and recommend state-of-the-art tools, technologies, and methodologies for test implementation.
• You are a self-starter, results-driven, working accurately and as team player striving for continuous improvement of test automation (hands-on, transformational and strategic)
• You become part of an extremely driven International cross-functional R&D team of the business unit Image Guided Therapy Systems R&D. Your local team is in Best (Eindhoven North), The Netherlands, and you will collaborate with other teams globally. Thereby making it a multidisciplinary international endeavour, where flexibility is key. Read more about our cardiology solutions via our site.

Minimum Required Qualifications ​

EducationBachelor's / Master's Degree in Computer Science, Software Engineering, Information Technology or equivalent.

Minimum 5 years of experience with Bachelor's OR Minimum 3 years of experience with Master's in areas such as Software Development, Software Design and Architecture, Testing and Quality Assurance or equivalent.

Preferred Qualifications

• You have 5+ years of experience in software development (C++, C#), combined with 3+ years experience in test and integration from lower level class/unit development, APIs, up to the larger system level.
• Experience in technical implementation of automation pipelines and practices like continuous integration, trunk-based development, automating the deployment process using test first approaches like developer-driven automated testing and shift left.
• Good abstraction skills and keep the high-level overview, you are not afraid to dig into the details, analyse, and solve issues when needed.
• Ability to communicate clearly both verbally and in writing, as well in creating clear architectural overviews and roadmaps. You can bring your point across to technical and non-technical stakeholders.
• Respected for being hands-on and fully up to speed with modern software test engineering methodologies (TDD, BDD and varieties of ATDD/executable specifications, test doubles)
• Passionate about coaching and implementing DevOps practices while applying latest software technologies and driving continuous improvement (i.e. via DORA metrics), given your up-to-date knowledge

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Your focus will be on supporting our imaging modalities Computed Tomography (CT).You will take ownership of challenges and demonstrate a proactive approach to finding solutions.

As server solutions and system communication play an increasingly important role in our services, expertise and interest in IT solutions will be a valuable asset.

Your role:

• Performing service activities such as regular preventive maintenance (PM), corrective maintenance (CM), troubleshooting, upgrades, installations, and modifications, in accordance with relevant Philips quality standards.

• Maintaining a holistic overview of the system and its functional environment, with attention to features from both a technical and user (clinical) perspective.

• Responsible for the completeness and accuracy of service data, with special attention to test and verification results.

• Timely and accurate submission of work reports, escalation reports, and other relevant administrative tasks as assigned.

• Timely escalation to our Western Europe service support organization.

• Reporting customer feedback and timely follow-up on relevant assigned quality and regulatory training.

You're the right fit if:

• 2 years of experience in IT, Network Diagnosis, System Connectivity, Remote Service within Engineering, Medical, Electromechanical Industries, or Science related environment or equivalent. Knowledge/Experience in Computed Tomography machines and systems as a plus.

• Familiar with computer tools and office software.

• Skilled in building and maintaining customer relationships and related contacts; team player.

• Independent and service-oriented with a logical and methodical approach to problem-solving.

• Structured, organized, with a high level of personal integrity and self-discipline.

• Fluent in spoken and written Dutch and English, Category B driver’s license – must have.

• Preferably hold a bachelor’s degree in Electronics / Mechanics or Electrical Engineering.

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Your role:

• Ensure the required EMC performance during the design, implementation, and verification of complex RF electronics systems

• Prepare and guide EMC (Pre-)Compliance tests of complex electronics systems

• Apply EMC standards to complex electronic medical systems

• Design, realize, and verify analog and complex RF (radio frequency) electronic circuits and systems

• Review PCBA designs on signal integrity and power integrity

• Stay up to date with developments in the field and propose ways to strengthen relevant team competencies

• Define the scope of activities and translate customer wishes into clear requirements and plans

• Provide input to project plans, including effort estimations based on requirements

• Report technical progress and outcomes to stakeholders through clear communication and documentation

• Build a strong network within and outside the organization to promote departmental competences and skills

You’re the right fit if you have:

• A Master’s degree in electrical engineering or a comparable field

• At least 10 years of experience in a product development environment

• Proven experience with the development of products compliant with EMC standards

• Hands-on experience with RF measurements and EMC tests

• Solid experience with complex electronic systems including RF

• Strong modeling and simulation skills (LTSPICE, Matlab/Simulink, HFSS/CST)

• A hands-on, pro-active, and can-do attitude

• A strong focus on quality and attention to detail, combined with a customer-oriented mindset

• Excellent communication skills in English

• Networking skills and a collaborative, team-player spirit

• Preferred is experience with medical product development and experience with working in multidisciplinary teams, including multi-site (i.e. global) development

• You are currently living in The Netherlands

This is an office role

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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• Discover .

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Beyond setting targets, you’ll serve as a technical coach, providing hands-on guidance to project teams and ensuring compliance with regulatory and internal quality standards. Your role will be pivotal in translating system-level requirements into actionable quality strategies, identifying risk early, and embedding reliability into every stage of development
Your role:

• Ensuring that appropriate Quality plans include all stages of the product’s lifecycle and support Quality Plan design for Software

• Validating key design inputs like usability, reliability, performance, supportability, manufacturability, localizability, safety, security, privacy serviceability, sustainability and costs

• Providing effective oversight on the execution of the Software Quality Plan, risk management activities and all design related activities during the lifecycle

• Leading quality problem solving

• Drive Design for Reliability and Design for Six Sigma

• Acting as a single point of contact in project teams for End2End Design Software Quality

• Ensure the voice of the customer is represented in project teams

• Using post-market data for analytics and statistics to report on the product’s performance in the market (provide feedback to manufacturing, suppliers, or design teams) and initiate field actions when required

• Ensuring the product’s design quality related requirements/criteria are complete and meet the Quality standards for every project milestone

• Making substantial contribution to integrate reliability engineering activities with the medical device development activities

You're the right fit if:

• Master’s degree or Bachelor's degree in engineering, science or a technical field.

• Minimum 7 years of experience in software engineering, software design or software development

• Prior experience in quality engineering or a demonstrated interest in quality-related disciplines is strongly preferred

• Certification in Design for Six Sigma (DfSS) at Green Belt or Black Belt level is advantageous

in-person at least 3 days per week.
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.
• Learn more about .
• Discover .
• Learn more about .