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Summary
About the Role
About You
- Minimum of 3+ years of Quality Engineering experience within FDA regulated medical device environments.
- Bachelor's Degree in Engineering, Quality, or related disciplines.
- Good understanding of Quality System Regulations (ISO 9001, ISO 13485, 21 CFR Part 803, 806 & 820).
- Experience in Design Quality/Control and Risk Management (ISO 14971).
- ASQ certifications such as Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), and/or DfSS Green Belt/Black Belt.
Benefits
- Competitive salary range of $97k–$156k.
- Comprehensive Philips Total Rewards benefits program including generous PTO, 401k (up to 7% match), HSA (with company contribution), and education reimbursement.
Over the past decade we have transformed into a focused leader in health technology. At Philips, our purpose is to improve people’s health and well-being through meaningful innovation. We aim to improve 2.5 billion lives per year by 2030, including 400 million in underserved communities. We see healthcare as a connected whole. Helping people to live healthily and prevent disease. Giving clinicians the tools they need to make a precision diagnosis and deliver personalized treatment. Aiding the patient's recovery at home in the community. All supported by a seamless flow of data. As a technology company, we – and our brand licensees – innovate for people with one consistent belief: there’s always a way to make life better. Visit our website: http://www.philips.com/ Follow our social media house rules https://www.philips.com/a-w/about-philips/social-media.html