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Group Leader & System Designer iApps
In this role, you have the opportunity to make life better
Looking at the challenges the world is facing today Philips’ purpose has never been more relevant. So, whatever your role, if you share our passion for helping others, you’ll be working towards creating a better and fairer future for all.
In this role you will bring innovative clinical solutions in 2D and 3D imaging and to our customers around the world. We help physicians to decide, guide, treat and confirm the right care in real time during a minimal invasive procedure to enable better outcomes for each patient. We touch patients’ lives when it matters most and we aim to do it in the most reliable, effective and sustainable way.
You are a part of
The System Design team of the Systems Engineering department in the Image Guided Therapy (IGT) Systems R&D organization. We are a team of highly skilled people in the system design, system verification, usability and validation and software development domains. We are located in Best, The Netherlands and in Bangalore, India and collaborate with other teams globally.
We make sure our products exhibit an excellent user experience and support physicians to provide the best treatment in the most demanding conditions, from cardiovascular to oncological and neurological treatment. We are a solution-based, customer-needs driven organization, working seamlessly across organizations to build the IGT of the future!
You are responsible for
Leading a full product(s) release cycle to ensure quality and compliance
Translation of user and business requirements into product requirements
Managing complexity of products in a multi-disciplinary and international set-up
Lead technically the requirements, design & product specifications for the system / subsystem.
Monitoring and managing that the requirements and design is implemented correctly by the Agile Release Train
Drive design for Quality, Reliability and Serviceability of the system / subsystem
Performing safety analysis according to applicable medical device standards
Complying to all applicable medical standards / regulations such as CE (EU-MDR) and FDA
Support regulatory submissions activities
Support project manager on realization, planning and budgets
Contributes to future studies, technical concepts and program roadmap
Support post market surveillance activities
Impact assessment, complaint Investigations and resolution
To succeed in this role, you’ll need a customer-first attitude and the following
Master's degree or equivalent in Engineering
Overall 15+ years of experience in the industry, several years of experience in designing & developing medical devices / products
Knowledge of IEC standards, risk management, verification and validation of software medical devices
Knowhow of design control processes for medical device design.
System thinking mindset and domain expertise in the related area.
Excellent communication skills
Team player
Leadership skills and drive for results
Why should you join Philips?
Working at Philips is more than a job. It’s a calling to create a healthier society through meaningful work, focused on
innovative, customer-first health technology solutions. Help us improve the health and well-being of billions of people, every year. Ultimately creating a career that no one could have planned for. Even you.
Visit our careers website to explore what it’s like working at Philips , read stories from our employee blog , find information
about our recruitment process and answers to some frequently asked questions .
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