Quality Engineer Market Returns Investigator Medical jobs at Philips in Netherlands

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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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 role:

• Leads the medical writing team in planning and delivering high-quality, compliant documents through effective resources, budget, and timeline management.
• Compiles and analyzes clinical and safety data to support medical device performance in alignment with EU regulatory standards (MEDDEV 2.7.1 Rev. 4, EU Medical Device Regulation).
• Author and maintain clinical documentation, including Clinical Evaluation Plans and Clinical Evaluation Reports, Post-market Clinical Follow-up Plans/Reports, and Investigator Brochures, contributing to Risk Management and Post-Market Surveillance activities.
• Drives collaboration and knowledge-sharing across medical, clinical, and regulatory teams, including Medical Affairs, Clinical Development, Research & Development, and Regulatory Affairs.
• Develops clinical evidence strategies for New Product Introductions, including performance claims and coordination on usability and non-clinical evidence.
• Collaborates with cross-functional teams to ensure regulatory compliance and to define medical writing scope and clinical evidence strategy.
• Optimizes medical writing processes by identifying and implementing automation, standardization, and workflow efficiencies.
• Translates complex scientific data into clear, impactful narratives for regulatory bodies, clinicians, and stakeholders to support product development and commercialization

You're the right fit if:

• You’ve acquired a minimum of 10+ years combined experience working within FDA regulated medical device and clinical environments, with a focus on the development of clinical evidence/documents (manuscripts, scientific abstracts, conference presentations/posters, reports based on clinical studies, and data/analytics).
• You have detailed knowledge of medical device regulations, requirements, and standards for FDA and EU especially for medium risk devices (Class II/Class IIA) focused on AI/software and information products.
• You have proven strategic/functional management experience in building and developing highly organized and capable teams. Experience in project management (a plus if you have experience in agile), mentoring, training, performance management and development of team members.
• You have a demonstrated track record of learning agility and comfort in taking on /shaping complex/uncertain business problems and creating creative/pragmatic solutions.
• You have a passion for simplification and optimizing processes and workflows, identifying opportunities for automation and software tools that improve productivity, compliance, and reduce time to market.
• You have a minimum of a Master’s degree in life sciences or equivalent discipline (REQUIRED).
• Preferred experience: Background in Real-World Data/Analytics (such as Epidemiology, Health Services Research, Health Economics or Medicine) and healthcare quality improvement. Project management background and familiarity with agile tools (Azure Dev Ops/Jira), information management (Confluence, Distiller, Endnote) or dashboarding/visualization (Tableau, PowerBI).
• Near-native level of English

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As Quality Director for the Premium and Clinical Segment in MR, you will lead and direct all aspects of quality assurance across the segment, driving strategic planning, compliance management, and business transformation for this segment. You will shape and execute quality strategies that ensure adherence to standards, regulatory compliance, and continuous improvement across the organization.

Your role:

• Lead quality assurance strategy development, execution oversight, and capability building to ensure compliance and excellence.

• Contribute to strategic planning by refining mission, vision, and policies to align with organizational goals.

• Oversee product release processes, ensuring compliance with safety and environmental regulations.

• Drive business transformation aligned with company strategy, enabling rapid growth through quality-led initiatives.

• Establish and manage supply chain quality assurance practices at the delivery model level.

• Direct product recall procedures, ensuring swift resolution and regulatory compliance.

• Own supplier qualification, audits, and assessments, and support internal and external audit readiness.

• Lead cross-functional discussions to resolve quality compliance issues and support business needs.

• Act as a senior-level expert, shaping company objectives and contributing creatively to goal attainment.

• Drive comprehensive talent management, including succession planning, performance management, and career development.

• Executes business transformation aligned with company business strategy, complies with quality regulations and budget, possesses a comprehensive grasp of solution strategy, facilitating end-to-end transformation for rapid growth, inclusive of skills and business partnerships.

• Oversees quality assurance activities, including strategy design, execution oversight, independent assessment, and compliance by design initiatives, and building and developing the quality assurance capability.

You're the right fit if:

• Bachelor’s degree in Engineering, Physics, or a related technical discipline.

• Over 12 years of experience in Quality, Regulatory Affairs, or Product Safety, with deep expertise in the medical device industry. Strong knowledge of ISO 13485, ISO 14971, and global regulatory frameworks including EU MDR and FDA.

• Demonstrated leadership in managing quality professionals, with a solid track record in people management.

• Extensive experience across the full spectrum of quality management, including CAPA, risk management, regulatory compliance, design quality, change control, and continuous improvement initiatives.

• Proven ability to lead teams and audits, develop strategic plans, communicate effectively across functions, and deliver impactful results with strong business insight.

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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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.

• Learn more about .

• 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 .