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Quality Manufacturing Engineer - Medical Technology (m/f/d):

In this role you will have the opportunity to guide, advise and support Business Categories, Markets and enabling functions to always do the right thing. This involves being a confident advisor and to always aim for creating products that deliver high quality and outstanding reliability to the lives they will improve. You are empowered to use your voice and expertise to have a positive impact on your team, our business, and health technologies that will improve the well-being and care for people around world.

Your role:

• You will be part of the Quality department that supports patient monitoring products and solutions. We ensure world-wide product approval and compliance with all applicable regulations and requirements.

• You and your team work closely together with our internal stakeholders in order to achieve timely releases of innovative products and processes that deliver high quality and outstanding reliability to the lives they will improve.

• You will be responsible for achieving a state of high-quality performance, compliance and sustainability in the factories while pursuing continuous quality improvement through the application of Quality Engineering practices.

• This flexible role offers you the opportunity to work with international teams, while benefiting from a hybrid working model (spend at least 3 days working from the office and up to 2 days from home).

• From a competitive salary to flexible working, a career at Philips comes with all sorts of wonderful benefits. Be sure to speak to your recruiter about benefits in your region.

You're the right fit if:

• You hold an Engineering degree in a relevant technical discipline or equivalent professional qualification and relevant practical experience

• You have 3+ years’ work experience as Quality Engineer in a highly regulated industry (preference for the medical device industry)

• You have strong experience with Process Validation methodologies combined with Risk management knowledge (e.g. PFMEA)

• You have experience handling non-conforming Products and CAPAs

• Knowledge and experience with application of Standards like ISO13485, ISO14971, 21CFR820 as well as working knowledge of ISO 2859 and ISO 3951 is preferred

• You are a social team player who thrives in a global cross functional environment

• You have good communication skills verbal and in writing

• You have a hands-on and solution-oriented mentality with a high focus on product quality

• You are business fluent in both English and German languages.

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 improve 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 commitment to diversity and inclusion here.

Equal Opportunities Disclaimer

We’re proud to be an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, pregnancy and pregnancy-related conditions, age, national origin, disability, protected veteran status, gender identity or any other factor protected by applicable federal, state, or local laws.

For more information, read our Inclusion and Diversity Policy and, to know more about your Human Rights, we encourage you to view this report.

For candidates with disabilities, we’re committed to supplying reasonable accommodations during the recruitment process, as well as when you enter our employment. If you need a reasonable accommodation because of a disability for any part of the employment process, please make your recruiter aware.

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