Careers in Quality

You're passionate about quality, and so are we.

Our quality control starts with our people. As a quality professional, we welcome your skills, expertise and capabilities. That's because you'll be safeguarding the quality, innovation, and value that our organization delivers all the time, every time to our patients, customers and partners.

Embrace your ‘quality gene' at Philips

Do you have the Quality Gene?

Quality is at the heart of everything we do at Philips, and it all starts from our biggest priority: our customer.

Quality Systems

Watch how Katherine Moehrke, Document Control Manager at Philips in Highland Heights, Ohio USA, makes sure we have the right product quality and comply with all regulations within healthcare technology.

Health Watch team

Watch how Vanja Hommes, Head of Regulatory and Clinical Affairs, ensures that quality is embedded in every step of the design process to help develop the Philips Health Watch.

China Imaging team

Watch how Senior Quality Systems Manager Xin Li ensures that internal quality systems at Philips' Suzhou office are running according to local safety and quality requirements.

A message from Philips CEO

A message from Philips CEO to Quality & Regulatory professionals about the importance of their work and their elevated importance to Philips Quality Transformation.

Our quality and regulatory function has recently been rebuilt under new leadership to propel this vital business area even further forward. This makes it an excellent time to join and spearhead our growing team. Together we'll affect improve billions of lives worldwide.

We're looking for fully fledged quality and regulatory professionals with strong technical skills, combined with the ‘quality gene' to join the team and make excellence just the start.

What do we mean by ‘quality gene'?

We use the term to define those who are brave perfectionists in all they do. You won't be afraid to do the right thing vs. the easy thing, even if it means going against the crowd. You'll thrive on leading change in times of diversity, and inspiring others to join you on that journey.

Our People & their stories

Ronit Dahan-Iluz - Quality and Regulatory Director

"Meet Ronit, Quality and Regulatory Director at Philips, who is leading and driving change for the better..."

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Mak Song Wen - Quality & Regulatory Specialist

"While I was a Bio-engineering undergraduate at Nanyang Technological University (NTU), I saw an opening for a Quality & Regulatory Specialist (Q&R) at Philips in an email from the school’s Career Affairs Office..."

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Katherine Moehrke - Document Control Manager

"Meet Katherine Moehrke, Document Control Manager, who provides essential quality checks and control to ensure all documentation and products are efficiently and correctly released in compliance with regulations..."

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Ling Xiao Yun – Post Market Surveillance

"Meet Ling Xiao Yun, Post Market Surveillance Manager, Shanghai, making a real difference to people's lives..."

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Vanja Hommes - Head of Regulatory and Clinical Affairs

"Meet Vanja Hommes, Head of Regulatory and Clinical Affairs at Philips, who helps design products of the highest standard..."

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Sarah Xu - Senior Regulatory Affairs Specialist

"Meet Sarah Xu, Senior Regulatory Affairs Specialist at Philips in Beijing, China, making a real difference to people's lives..."

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Life at Philips

It takes multiple expertise to build continuous improvement

"It sounds like a daunting task: build a flexible suite of continuous improvement solutions that provide a path to help find and maximize opportunities for doing more with less, all the while helping focus on patient care requires a multi-disciplinary approach and a unique focus on quality..."

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Our culture: How we make life better

Everything we do at Philips is about making life better for people around the world. How? By creating meaningful innovations that solve a range of healthcare challenges big and small. Working together with us you’ll be part of a diverse global culture that puts people first: our own and our customers.

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4 Tips to ensure your team is ready for the EU MDR

The new EU Medical Device Regulations (EU MDR) go into effect in 2020. To the rest of us that may seem like a long time, but for companies marketing— or planning to market—their devices in Europe the clock is already ticking. The sweeping regulations will likely affect the marketing of most CE-marked devices.

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