דרושים Developer Pulse Programming Clinical Mri 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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Your role:

• Provides expert guidance to customers on complex clinical procedures and protocols, leveraging deep knowledge and experience to optimize the performance and utilization of equipment.
• Takes a proactive approach in managing customer escalations, complaints, and feedback, independently assessing situations and implementing effective strategies to address concerns and maintain customer satisfaction.
• Applies specialized knowledge in breadth and/or depth to a variety of issues and projects within the team, ensuring effective solutions and innovative approaches to complex challenges.
• Works under limited supervision and broad guidelines, regularly applying independent judgment on matters of significance to drive project success and compliance.
• Collaborates across multidisciplinary teams, including product development, research and development, and regulatory affairs, to drive innovation and improve product performance based on customer insights.
• Leads initiatives to enhance the organization's clinical support capabilities, including the development of new training materials, processes, and tools, to ensure continuous improvement and excellence in customer service delivery.
• Undertakes complex clinical or system application assignments, exercising autonomy and discretion in decision-making, and adapting to evolving circumstances to achieve desired outcomes.
• Takes ownership of documenting and maintaining service records with meticulous attention to detail, ensuring accuracy and completeness within the Service Management System.
• Conducts thorough investigations into customer complaints or escalations, gathering relevant data and evidence to facilitate resolution and prevent recurrence.
• Stays updated on new product releases, software updates, and industry developments through ongoing training, self-study, and participation in education programs and industry events.
• Develops and maintains strong relationships with healthcare professionals by actively participating in discussions, providing ongoing support, and soliciting feedback, ensuring that their concerns are effectively addressed.

You are fit if:

• Hold a Bachelor’s or master’s degree in engineering , Medical, Science, or a related field.
• Have 2+ years of experience in the medical industry, clinical support, healthcare, or customer service.
• Demonstrate deep clinical expertise and confidently guide customers on complex procedures and equipment usage.
• Proactively resolve escalations and complaints, ensuring high customer satisfaction.
• Apply specialized knowledge to solve complex challenges and drive innovation.
• Work independently, exercising sound judgement under broad guidelines.
• Collaborate effectively across functions like R&D, product development, and regulatory affairs.
• Lead initiatives to enhance clinical support through training tools and process improvements.
• Manage complex clinical or system assignments with autonomy and adaptability.
• Maintain accurate service documentation with meticulous attention to detail.
• Investigate customer issues thoroughly to drive resolution and prevent recurrence.
• Stay current with product updates, software releases, and industry trends.
• Build strong relationships with healthcare professionals, actively listening and responding to their needs.

Onsite roles require full-time presence in the company’s facilities.

This role is an office-based role.

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Your role:

• You are part of The Cardiology Informatics Clinical Excellence team. The Cardiology Informatics team in Eindhoven (within the Philips' Enterprise Informatics business group), a leader in cardiology informatics solutions with over 5000 customers globally. You will work closely with global ISCV customers and clinical application specialists, and the Cardiology Informatics R&D teams located in Eindhoven (Netherlands), Bangalore (India) and Blumenau (Brazil).
• Serve as a Clinical Application Specialist collaborating closely with global ISCV R&D development teams.
• Define clinical requirements and provide support to R&D, focusing on refining clinical features, prioritizing customer feedback, validating products, leading clinical testing, assessing risks, and understanding regulatory factors.
• Translate clinical requirements from customers, product management, and marketing to engineering teams for efficient development and verification processes.
• Conduct training sessions for field clinical application specialists and customers on new clinical features and products, while keeping abreast of the latest innovations in cardiology imaging.
• You'll build and maintain strong relationships with validation and collaboration sites.
• Discover the many benefits of a career at Philips. Speak with your recruiter to learn more about the benefits available in your region.

You're the right fit if:

• You hold a Bachelor's or Master’s degree in Ultrasound.
• You have 3+years of sonography experience, knowledge in usage of ultrasound and product features within the cardiology domain.
• You can understand, convey, and teach others the clinical workflows in cardiology specialties and technical use of the specific solutions.
• You have high energy, and self-driven mentality.
• You have an affinity with IT Solutions, you will be able to liaison between clinical and technical conversations.
• You are highly flexible and motivated team player, who can establish relationships with both internal and external customers.
• You are familiar with Philips products, such as IntelliSpace Cardiovascular, Xcelera, XperIM or Philips Ultrasound.
• You have excellent customer-centric & communication skills.
• You are fluent in Dutch and have a good command of English in written word and speech
• You are willing to travel up to 15% of your time and are able to travel globally on a short notice to meet with our customers.

This role 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 improve the lives of others.

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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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• Discover .
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Your role:

• Support the evaluation of innovative (AI) solutions and technologies, contributing to the assessment of their potential to address identified needs and challenges.
• Develop clinical evaluation documentation supporting regulatory submissions and post-market clinical surveillance strategy.
• Define and execute (internal and external) clinical and performance studies, leading in protocol development, data collection, and analysis, ensuring robust scientific methodologies.
• Perform quality reviews, tracking, document control, and management of essential study, clinical evaluation and clinical post market documents.
• Assist in the preparation of strategic thought leadership materials, including reports, presentations, and publications, to support marketing strategies and organizational objectives.
• Act as author for documentation and publications resulting from clinical studies, literature reviews, and other research related activities, sharing insights and findings with relevant stakeholders to advance knowledge and drive impact.
• Conduct research to identify emerging customer needs and trends within the specified domain of diagnosis, treatment, and patient care, informing strategic decision-making and product development initiatives.
• Implement research initiatives, including intellectual property (IP) assessment, contributing to the development and execution of research protocols.

You're the right fit if:

• PhD Degree in Biotechnology, Pharmacology, Biomedical Sciences, Artificial Intelligence, or an equivalent field (preferred).
• Master's Degree in Biotechnology, Pharmacology, Biomedical Sciences, Artificial Intelligence, or an equivalent field, with a strong understanding of research methodologies, clinical study design according to Good Clinical Practices (GCP), and Statistics.
• Additionally, demonstrated relevant experience in technical domains such as advanced image processing, Artificial Intelligence, or nuclear medicine is preferred
• At least 3 years of experience in areas such as Clinical Research or Clinical Trials, preferably within the Medical Devices or Pharmaceutical Industry, or an equivalent field. With a PhD, No prior experience required.
• Strong knowledge of Biostatistics.
• Basic understanding of medical imaging or imaging pros-process (is a plus).
• Experience as a medical/scientific writer or in an equivalent role.
• Knowledge of regulatory processes (preferred).

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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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 .

You are responsible for

• Managing Supplier Relationships, Performance and Contracting based on clear targets and ongoing Business Review Meetings with key suppliers.
• Defining and managing a strong funnel approach of Procurement (Price) and Demand (Quantity) initiatives.
• Program managing the execution of the Funnel initiatives in alignment with Business/Markets/Functions.
• Planning and executing Supply Base Optimization actions and negotiating roadmaps with suppliers by applying game theory and e-Sourcing at scale.
• Developing a Supply based strategy including Playbooks to guide supplier management

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

• University or master’s degree in a relevant technical field or equivalent.
• Minimum 8 years’ experience in Strategic/Category Sourcing, Commodity Management and/or Supply Chain Management or comparable roles.
• Strategic sourcing experience in Logistics categories such as Warehousing and Road transportation.
• Proven capability in managing complex global suppliers on senior management and executive level.
• Solid track record in achieving superior negotiation results by applying creativity and innovation in your negotiation approach.
• Exceptional Communication and Negotiation skills (e.g. Game Theory).
• Experience in supplier strategy development
• Independent thinker with strong networking & influencing skills on senior business management and executive levels (internal and external).
• Dynamic and inspiring leader who can lead virtual teams
• Languages: full professional English and Chinese (both written and verbal)

• Experience in working with best-of-breed sourcing tools
• Availability to travel

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