Philips

Hardware Integration Engineer

Posted Jun 11, 2025
Project ID: PHIAJP00002363
Location
Best
Hours/week
40 hrs/week
Timeline
11 months , 4 weeks
Starts: Jul 1, 2025
Ends: Jul 1, 2026
Payrate range
5000 - 6000 €/month
Application Deadline: Jul 1, 2025 12:00 AM

Hardware Integration Engineer


You are responsible for

  • Setting up, preparing, executing, and documenting hardware element and part level specifications, designs and tests, for both functional as well as non-functional aspects based on the overall hardware strategy.

  • Defining and maintaining requirements, design, implementation, test and integration of module/sub- system in accordance with the higher-level architectural requirements and design specifications.

  • Producing high quality documentation with solid arguments backed by evidence. Ensuring that the design is consistent with the higher-level architecture and requirements.

  • Reviewing product specifications, writing test protocols and acceptance criteria, and executing, and documenting element and part level tests.

  • Determining the approach for element/part acceptance tests (including basic safety and EMC).

  • Contributing to the hardware test strategy, driving automated testing & hardware test.

  • Supporting regulatory submissions activities to comply with all applicable medical standards/regulations, life cycle management, complaint investigations, and post-market surveillance activities.


To succeed in this role

You should have the following skills and experience:

  • Bachelors or Master's degree in Electrical Engineering or equivalent relevant degree.

  • A solid track record in creating audit-proof documentation.

  • The ability to absorb large amounts of information and compress that into understandable bite-sized clear and succinct documents for both technical and non-technical stakeholders.

  • Experience with releasing Medica Device Products to the market, from conception to full scale production and life cycle management.

  • A minimum of 10 years of experience in designing and testing electronics system elements or parts.

  • Prior experience in engineering quality in the context of medical device development (documentation, traceability, sourcing) and quality systems.

  • Expert in Basic Safety 60601-1 Familiarity with EMC 60601-1-2, Quality Management 13485, and risk management standards 14971 for Medical Devices.

  • Experience using laboratory tools equipment such as oscilloscopes and soldering stations, etc. High quality standards and a drive for continuous improvement.

  • Taking ownership with a pro-active mindset and eager to learn.

  • Tool experience: knowledge of PLM database(s) (i.e. Windchill is a plus) and requirements/test case management tools (e.g. DNG, Doors) and proficiency in MS Office suite.

  • Hybrid way of working, 3 days at the office at minimum.



Please take these minimum requirements into consideration for this position.

Education

  • Bachelor's / Master's Degree in Electrical Engineering, Electronic Engineering, Mechanical Engineering, Computer Science Engineering or equivalent.


For this project, you’ll work for Philips and become a contract or permanent employee of a Randstad company. As a contractor at Philips, you'll enjoy cutting-edge challenges and unexpected experiences that make you a more in-demand professional.

Why work on a project at Philips?

If you’re looking for meaningful work and a chance to tackle complex challenges, broaden your skills and expertise, and become an even more sought-after professional, you’ll find all that and more with project work



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