Job Title: Senior Design Quality Engineer - Systems & Innovation
Job Description
In this role, you have the opportunity to
Drive Design Quality for innovation projects by shaping patient safety, product quality, and reliability early in development. In this senior role, you will execute our shift-left strategy across the V-model, influencing requirements, risk controls, verification, and design decisions to help teams prevent issues upstream and deliver safe, effective, and high-quality product releases.
You are responsible for
Lead Design Quality for multidisciplinary product and systems developments, ensuring quality is built in from concept through release. Drive shift-left quality by strengthening requirements, traceability, risk management, and verification strategies early in development.
Guide teams on system decomposition, interfaces, integration risks, and design control deliverables so development decisions are robust, timely, and evidence based.
Support reliability planning and execution activities, including accelerated testing, field-feedback-driven improvements, and reliability growth initiatives.
Partner with R&D, Systems Engineering, V&V, Regulatory, and Operations to influence technical decisions and improve product safety, quality, and reliability.
Support, challenge, and influence verification and validation strategies, driving statistically justified and risk-based approaches. Lead and coach structured risk management activities, including DFMEA and FTA, ensuring risk controls are translated into requirements and verified effectively.
Use verification, validation, and post-market learning to strengthen design choices, release confidence, and continuous improvement.
You are a part of
You will join a high-impact Design Quality team supporting complex, multidisciplinary product and systems developments in a regulated environment. We are looking for a senior quality leader who can influence early design decisions, challenge constructively, and help teams embed proactive quality practices that improve patient safety, product quality, and innovation outcomes.
To succeed in this role, you should have the following skills and experience
Bachelor’s degree in Engineering with 12+ years of relevant experience, or a Master’s degree with 8+ years of relevant experience, preferably in Systems Engineering, Reliability, Design Quality, or product development within the medical device, health technology, or another highly regulated industry.
Proven ability to influence cross-functional stakeholders across R&D, Systems Engineering, V&V, Regulatory, and Operations to improve development quality and support sound design decisions.
Strong experience in complex product development, ideally including multidisciplinary systems and software-enabled products, with the ability to engage early in the design process and drive proactive quality.
Demonstrated experience with requirements quality, traceability, interfaces, integration, risk management, and risk-based verification and validation planning in a regulated environment.
Preferably certified in Design for Six Sigma (DfSS) at Green Belt level, with willingness to develop further towards Black Belt certification.
Strong experience in structured problem solving, root cause analysis, and risk-based decision-making, using methods such as 8D, DMAIC, DFMEA, FTA, or similar.
Good understanding of medical device regulations, standards, and design control expectations, such as 21 CFR 820, ISO 13485, EU MDR, IEC 60601, IEC 62366, IEC 62304, and ISO 14971.
Strong interpersonal, written, and verbal communication skills, with the credibility to challenge constructively, coach teams, and influence senior stakeholders.
Available to work on site at least 3 days per week.
In return, we offer you
You will join a challenging and innovative environment with strong opportunities to grow your career and expand your impact. We offer a competitive package designed to support your professional development, wellbeing, and work-life balance.
Competitive salary and variable bonus based on company results and individual performance
25 days of leave, with the option to purchase up to 20 additional days annually
Personal development support, including training, coaching, and career growth opportunities
Solid pension scheme and attractive collective health insurance package
Opportunities to purchase Philips shares and products at a discount
A healthy work-life balance in a flexible and supportive environment
Skills Required
- Bachelor's or Master's engineering degree
- 12-14 years of experience in Quality or Reliability Engineering
- DfSS Green Belt certification
- Experience with medical device regulations
- Strong experience with Systems Engineering methodologies
Philips Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Philips and has not been reviewed or approved by Philips.
-
Retirement Support — Retirement support is positioned as a standout, including a strong 401(k) match (often described at 7%) alongside pensions in some contexts.
-
Flexible Benefits — Flexible benefits are emphasized through choice in health insurance options and a broad “Total Rewards” approach that combines compensation, health and wellness, and work-life support.
-
Leave & Time Off Breadth — Leave and time off breadth appears strong, with generous paid time off and policies covering parental leave, caregiving responsibilities, volunteering, and family medical leave.
Philips Insights
What We Do
Do the work of your life to help the lives of others. As a leading health technology company, it is our purpose to improve people’s health and well-being through meaningful innovation. Our goal is to improve 2.5 billion lives per year by 2030. We also strive to be the best place to work for people who share our passion, by promoting personal development, inclusion and diversity while acting responsibly towards our planet and society.






