EMC Verification Engineer

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 the (EMC) Verification Engineer role you will be a part of the multidisciplinary IntraSight Hardware Team and you will bring innovative 2D and 3D imaging clinical solutions 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 responsible for

• Setting up, preparing, executing, and documenting hardware element and part level and tests, specifically with focus on EMI/EMC, as well to a minor degree other functional and non-functional requirements based on the overall hardware strategy.

• Defining and maintaining test strategies, test plans and test cases at system level (with special emphasis on EMC) and at integration of module/sub- system level in accordance with the higher-level architectural requirements and design specifications.

• Producing high quality documentation with solid arguments backed by evidence.

• Ensuring that test cases are 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.

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

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

• ISTQB Advanced certificate (Must)

• 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 (Medical Device) Products to the market, from conception to full scale production and life cycle management.

• A minimum of 10 years of experience in EMC testing.

• Experience in the Medical Device industry.

• Prior experience in engineering quality in the context of medical device development (documentation, traceability, sourcing) and quality systems. Expert in EMC 60601-1-2.

• Familiarity with Basic Safety 60601-1, 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.