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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.

We focus on doing Quality right

We get it, not everyday is easy working in Quality & Regulatory. Somedays can be stressful, but know that at Philips we have your back and we make sure that we focus on doing Quality right.  Quality is at the heart of everything we do.

Our journey in health technology
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Learn about our strategy to address global healthcare challenges and extend our leadership in the health technology industry. 

Embracing the unexpected is a fantastic opportunity to learn and grow

As a professional with quality in his DNA it’s no surprise Quality Site Leader Jon has a keen eye for detail and a methodical approach.  But happens when things don’t quite go to plan?  

A message from Philips CEO

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

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Philips’ quality and regulatory function has recently been rebuilt under new leadership to propel us even further forward. Our renewed sense of purpose makes this an excellent time to join and spearhead our growing team. Together we'll improve billions of lives worldwide. 

We're looking for fully fledged quality and regulatory professionals with strong technical skills and an innate ‘quality gene' to join the team and make excellence our standard operating procedure.

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Do you have the Quality Gene to be a part of Philips Quality & Regulatory team?

What do we mean by ‘quality gene'?

We use the term to define the perfectionists, the brave professionals who aren’t afraid to do the right thing versus the easy thing, even if it means going against the crowd. You'll thrive on leading change within diverse initiatives, and inspiring others to join you on that journey.

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Our people and 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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Xin Li -  Senior Quality System Manager
"At Philips, everything we do is fuelled by three things: “professional knowledge”, “communication skills” and “important responsibility”. The work we are doing here is changing the world as it is right now..."
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..."
Ling Xiao Yun – Post Market Surveillance
"Meet Ling Xiao Yun, Post Market Surveillance Manager, Shanghai, making a real difference to people's lives..."
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..."
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..."

Our newest blog articles

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The 5 Most Commonly Asked Questions by Q&R Candidates
"We expect to ask our potential Quality hires a lot of smart questions. But job candidates often have good inquiries for us, as well. From the Q&R structure at Philips to the culture to the opportunities for professional growth and advancement, Quality professionals want to know what it's like to work for one of the world's largest health technology companies...."
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Do not fear change. For Philips, change means opportunity
"Do not fear change. I believe most Quality professionals agree with this statement. Change is something that’s inherently part of the medical device industry. We focus so much time and energy on continuous improvement that compared with other professions we are better prepared to be change agents. For Philips, change means opportunity...."
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4 tips for ensuring your regulatory team is ready for the new 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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