At Philips, we believe there’s always a way to make life better.
As a Project Support Engineer within the Business Category Hemo, you will support controlled product and component lifecycle execution across the Hemo portfolio, ensuring compliant, on-time delivery of maintenance activities and product releases. In this role you will execute small to medium-sized product, quality, and maintenance projects within the Hemo product portfolio.
Ensure assigned deliverables to the project team comply with QMS and regulatory requirements, operating within the strategy defined by the Program Manager.
Manage small maintenance projects, including hardware updates, CBOM adjustments, and field-driven product improvements.
Coordinate amongst others risk assessments, cross-functional inputs, and controlled execution.
Manage engineering documentation and controlled changes in documentation system (Windchill), ensuring accuracy, traceability, and compliance across configurations and revisions.
Maintain commercial and production documentation (CBOMs, Production Data Packages), supporting alignment with engineering, commercial, and manufacturing stakeholders.
Support procurement activities for the Business Category through Purchase Requisition and Purchase Order creation to enable timely acquisition of materials and services.
Support major product releases within the Business Category by managing defined work packages, securing documentation inputs, and coordinating small-scope deliverables.
Monitor project risks tracks progress within defined Way of Working, and provides clear updates for assigned tasks and projects to the Program Manager and cross-functional teams.
Collaborate closely with engineering, operations, quality, supply chain, and manufacturing to ensure consistent execution of product and component lifecycle changes and maintenance activities.
You have a Bachelor’s degree in a technical discipline (e.g., Mechanical, Electrical, Biomedical, or Industrial Engineering) or equivalent professional experience in a high-tech, highly regulated environment.
You bring 2+ years of experience coordinating and executing technical projects or product lifecycle and maintenance activities within a regulated industry (e.g., medical devices, healthcare, or similar).
You have hands-on experience with engineering documentation systems and controlled change management, including configuration management, lifecycle documentation, documentation reviews, and risk assessments.
You are a strong cross-functional collaborator, comfortable working with engineering, quality, supply chain, and manufacturing teams, able to navigate structured processes and regulatory requirements, and fluent in English (spoken and written).
How we work together
We believe that we are better together than apart. Onsite roles require full-time presence in the company’s facilities. This role is an onsite role.
About Philips
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 our business.
• Discover our rich and exciting history.
• Learn more about our purpose.
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 here.
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