Senior Design Quality Engineer

Are you an experienced professional with a passion for quality and medical innovation? Do you want to play a key role in ensuring the safety and reliability of advanced medical systems that save and improve lives? Then the role of Senior Design Quality Engineer at Philips IGT Systems is for you.

Your Role

As a Senior Design Quality Engineer, you are the strategic leader who sets quality and reliability standards for medical products. You coach and support project teams, ensuring that these innovations not only meet the highest requirements but even exceed them. You act as the crucial link between product development and real-world experiences.

Your Responsibilities

• Define Quality Strategy: You develop the strategy for patient and user safety, quality, and reliability for the entire product lifecycle.

• Oversight and Supervision: You provide effective oversight of the execution of quality plans and risk management activities from start to finish.

• Expert Guidance: You are the go-to subject matter expert for project teams and departments on Design Control and quality standards.

• Lead Problem-Solving: You are responsible for leading teams in resolving quality-related issues.

• Data Analysis: You use data from products already on the market to initiate design adjustments and continuously improve the products.

• Verification and Validation: You validate key design inputs and collaborate with V&V teams to ensure thorough testing.

Your Team

You will be part of the global Philips Patient Safety & Quality organization, within the Design Quality team of our IGT-Systems Business. Together, we constantly strive for product quality improvements to exceed the expectations of both internal and external stakeholders.

What You Bring

We are looking for an inspiring leader who sees excellence as a way of life and can motivate others to prioritize quality above all else. You have a sharp analytical mind and are a proactive, critical partner.

• A Bachelor's degree with 12+ years or a Master's degree with 8+ years of experience, preferably in a Quality or Reliability Engineering role in the medical or aerospace industry.

• Experience with Design Controls and leading FMEA activities.

• Knowledge of global medical regulations and standards, such as ISO 13485 and EU MDR.

• Experience with Systems Engineering and problem-solving methodologies (root cause analysis).

• Skilled in analyzing development and field data to improve the performance and safety of products.

• Excellent communication, consultancy, and project management skills.

• The willingness to work in the office at least 3 days a week.

You will be employed by a Randstad company.