Senior Connectivity Ip Counsel jobs at Philips in Netherlands, Eindhoven

Your role:

• Champion collaboration between the business community and BPO’s for Export Control, tackling supply chain bottlenecks and ensuring seamless ERP process integration for GTS, while partnering with Business Analysts and Functional Consultants to ensure alignment.

• Lead as the product owner for the project scrum team, ensuring processes are designed to requirements, delivered as envisioned, and documented in alignment with the Philips Process Framework.

• Translate user requirements into a clear, prioritized user story backlog and drive transformation by clarifying the impact of new solutions and ways of working across IT, data, people, and processes.

• Enable learning by delivering process training, building competencies, and preparing engaging end-user documentation.

• Evaluate and refine process change proposals, escalating relevant ideas to BPOs, supporting local improvements, and sharing best practices with other BPEs.

You are the right fit if:

• Hold a bachelor’s or master’s degree in Business, Economics, Supply Chain Management, IT, or Industrial Engineering & Management Sciences, and bring 5–7 years of proven experience in supply chain management, trade compliance, and/or IT.

• Demonstrate strategic thinking with the ability to see and shape the bigger picture, and leverage strong knowledge of SAP ERP, SAP-GTS, and their organization-wide implementation.

• Offer expertise in trade compliance (export control) and its application within SCM/Operations, with an affinity for the healthcare and personal health business.

• Inspire others with strong influencing and communication skills, acting as a bridge builder, while taking decisive action and showing initiative.

• Apply proven change management skills, think analytically, and contribute as a collaborative team player.

• Communicate fluently in English (verbal and written) and in the local language.

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

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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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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Senior Mechatronics Systems Technologist

You willacross Innovation Engineering. Help shapein Mechatronics aligned withand. Serve as abetween cutting-edge academic/industry research and practical application within regulated medical device environments.

Your role:

Technology Leadership:

• Define and evolve the mechatronics technology roadmap, with a strong link to digital- and AI applications.
• Identify gaps in current capabilities and develop plans to close them.

Expert Contribution:

• Drive mechatronics design in product and system development, including modeling, simulation, and analysis.
• Select optimal sensing and actuation strategies, and apply advanced control techniques including AI-based methods.

Competence Building:

• Mentor team members across locations (e.g. Eindhoven and Pune).
• Be a trainer – take ownership of the Mechatronics training curriculum and organize company-wide trainings with support of the Philips University
• Champion AI, model-based design, and system performance innovations.

Stakeholder Engagement:

• Act as an internal consultant across projects.
• Engage externally with universities, consortia, and industrial networks to stay ahead of trends and attract top talent.

You're the right fit if:

Must-Have Qualifications:

• Academic thinking level: PhD or MSc in Mechanical, Electronics, or Mechatronics Engineering (focus on Dynamics & Control ).
• 10+ years of experience in mechatronics and hardware/system design.
• Deep expertise in control theory , sensing & actuation , and AI for control systems .
• Strong stakeholder and communication skills.

Strong Preferences:

• Demonstrated leadership in regulated product development (preferably medical devices).
• Thought leadership presence (conference speaking, academic collaborations).
• Systems Engineering familiarity (V-model, requirements management).
• Risk and quality compliance: ISO-14971, ISO-13485, EU-MDR.
• DfSS/DMAIC certification (Greenbelt or Blackbelt).
• Experienced in Matlab/Simulink, AI tooling (e.g., ML models, neural nets, MPC).

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 .

Support the Multi-Vendor Services (MVS) Biomedical business as an entry-level Portable Equipment Handler, located onsite at a customer facility in Valhalla, NY. This role will provide administrative support to the onsite biomedical team.Your role:

• Provide an outstanding customer experience, become a viable team member, and quickly get up to speed with technical expertise.

• Identifying and resolving customer issues, providing the customer with the appropriate communication, and involving appropriate site service personnel.

• Responsible for customer relationship management through the effective use of technical knowledge to inspect, ship, and maintain low-risk biomedical equipment at customer sites; generate service revenue; adhere to state and federal regulatory requirements.

• Shift time: Monday - Friday: 7 AM - 3 PM, with opportunity for overtime on weekends. Must have the ability to work flexible hours, as needed based on business needs.

• May attend factory training classes and apply lessons learned through on the job training (OJT) and experience.

You're the right fit if:

• Ability to be onsite inValhalla, NY.

• High school graduate or vocational certification in electronics, biomedical equipmentservicing/engineering,or equivalent combination of education and experience in the electronics industry.

• Experience with biomedical equipment or administrative backgrounds in a healthcare/medical setting preferred.

• May require travel to customer sites other than assigned site, zone office, or identified locations for meetings. Occasional overnight stays and travel by air or train may be required for training.

• Ability to understand and utilize technical vocabulary to perform tasks according to either verbal or written instructions.

• Ability to display strong organizational and multi-tasking skills, self-discipline, and autonomy to work independently in a high-pressure environment.

• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this.

This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.

We are seeking a highly motivated Senior Information Security Manager to lead the design, implementation, and oversight of our strategic security initiatives across IT, Integrated Supply Chain (ISC), and Operational Technology (OT) environments. While prior experience in OT security is a plus, strong IT security professionals eager to grow into the OT domain are encouraged to apply.

In this pivotal role, you will protect sensitive data, ensure system integrity, and mitigate risks—all while ensuring compliance with regulatory requirements such as NIS2, HIPAA, EUMDR and FDA standards.

Security Strategy & Risk Management

• Develop and execute a comprehensive IT and OT security strategy aligned with industry best practices.

• Identify, evaluate, and mitigate security risks across IT, supply chain, and OT environments.

• Drive Security Projects, Programs & Initiatives across different locations

• Maintain regulatory compliance with HIPAA, FDA, and other relevant standards.

Security Architecture & Operations

• Design and maintain secure architectures for both IT and OT systems.

• Implement and manage firewalls, IDS/IPS, and advanced security tools such as Nozomi Guardian

• Define and enforce security frameworks and policies specific to supply chain technologies.

Incident Response & Threat Management

• Develop and lead end-to-end incident response plans and security playbooks.

• Conduct regular risk assessments and implement remediation strategies with minimal operational disruption.

• Perform threat modeling (e.g., STRIDE, PASTA, DREAD) and simulate cyberattacks to test resilience.

• Utilize the MITRE ATT&CK framework to analyze adversarial behavior and implement countermeasures.

Compliance & Governance

• Partner with service owners to continuously improve technical and administrative security controls.

• Define, monitor, and report on key security metrics and KPIs.

• Collaborate with the Philips Security Office and broader governance teams to align initiatives and drive continuous improvement.

Vendor & Stakeholder Engagement

• Lead supplier security assessments and ensure compliance with enterprise and regulatory standards.

• Promote security awareness and deliver training across internal teams and external partners.

• Serve as a trusted advisor to stakeholders on evolving threat landscapes and proactive defense strategies.

You're the right fit if you have:

• Bachelor’s or Master’s degree in Information Security, Computer Science, or a related field.

• 8+ years of experience in cybersecurity, with proven leadership in enterprise environments.

• Knowledge of OT security is preferred but not mandatory—willingness to learn and adapt is key.

• Strong experience with security tools, frameworks, and standards.

• Excellent communication skills, with the ability to influence across all levels of the organization.

How we work together:

This role is an office-based 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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As a Senior Model-Based System Engineer (MBSE) at Philips, you will be responsible for applying and improving the MBSE approach in various projects for different Philips businesses. You will play a crucial role in delivering high-quality (sub) systems models of products by meeting user and business requirements, managing complexity, providing technical leadership, and stakeholder management. Additionally, you will contribute to improving Systems Engineering capability across Philips by defining methods and setting up Philips standards for MBSE, coaching, and training others.

Your role:

• What we do today affects someone’s life tomorrow; it is a quality policy of Philips. Striving for the highest quality of healthcare products, you will be working on implementing and applying Model-based Systems Engineering (MBSE) in R&D departments within various Philips businesses. Your knowledge and skills will help us continuously improve our Systems Engineering practices and prepare us for the future.

• You will be a part of the Model-Based Systems Engineering competence group within the Innovation Engineering central function, primarily located in the High Tech Campus in Eindhoven. The MBSE group comprises of approx.15 highly skilled and motivated MBSE professionals working on different projects across all Philips businesses. These projects can cover every phase of the product life cycle, from development, manufacturing, market deployment, operation, and maintenance to phase-out. You will also help to deploy MBSE capability throughout the global company by creating and providing training and coaching and/or leading a team of system engineers.

• In this role, from being on the front-end of Philips product development through MBSE deployment activities, you will be able to guide every aspect of MBSE and product development at Philips. Our external engagement with other companies will allow you to also build a strong network of same-minded professionals across High Tech industry.

You're the right fit if:

• 7+ years of experience in an R&D environment in a regulated environment (a medical device company is strongly preferred).

• You are all-round System Engineer, an expert on Requirements Engineering, Risk Management and design.

• You have strong experience in Model Based System Engineering with tools e.g. Cameo and their customization e.g. Structured Expressions, Scripting, Profiles, Custom Diagrams, Validation Rules philosophy and implementation, Plugin Development etc.

• You have experience with SysML at least in Model User Level and with scripting as a plus.

• You are familiar with Structure, Behavior, Requirements and Parametric Models implementation.

• You are able to create MetaModel and DataModel definitions.

• You have a M.Sc. degree in Software, System, Electrical or Mechanical Engineering or in a similar field.

• You are an excellent communicator who can operate on different levels of architectural details with a hands-on mentality.

• Fluent in English

• You are living in the Netherlands

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

This is an office-based 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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Help shape the future of healthcare by designing safe and intuitive diagnostic imaging systems. As a Senior Usability Designer, you will apply human factors and usability expertise to ensure Philips DXR products meet user needs and regulatory requirements—enabling clinicians to deliver faster, more effective care.

Your role:

• Make a greater impact by improving the safety, usability, and effectiveness of our Diagnostic X-ray systems, directly supporting better outcomes for patients and caregivers.

• Collaborate with cross-functional teams—including engineering, clinical, marketing, quality, regulatory, and service—to deliver human-centered solutions that meet global medical device standards.

• Conduct and lead user research, usability testing (formative and summative), task analysis, and risk assessments (usability FMEA), and generate documentation for regulatory submissions (FDA, EU-MDR, CMDE).

• Stay ahead of usability regulations (IEC 62366, ISO 14971, FDA guidance) and advise teams on compliant, user-focused product development.

• You’ll work in a dynamic and collaborative team, with access to a global network of usability experts. The role offers significant personal and professional growth opportunities in a creative, high-impact environment, with strong support for continuous learning and career progression.

You're the right fit if:

• You bring 5+ years of experience in usability , human factors, or user-centered design—ideally in medical devices or other high-regulation industries (aviation, automotive, military).

• You have strong research and communication skills , with the ability to translate user needs into actionable design input and strategic direction.

• You hold a degree in Industrial Design, Product Design, Cognitive Psychology , or a related field with a focus on Human Factors or Human-Computer Interaction (HCI) .

• You’re familiar with medical device usability and risk management standards (e.g., IEC 62366, FDA guidance, ISO 14971, EU-MDR ).

How we work together

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