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Design Quality Engineer

Job in Aberdeen, Harford County, Maryland, 21001, USA
Listing for: Philips Benelux
Part Time position
Listed on 2026-07-06
Job specializations:
  • Engineering
    Quality Engineering, Regulatory Compliance Specialist
  • Quality Assurance - QA/QC
    Quality Engineering, Regulatory Compliance Specialist
Job Description & How to Apply Below

Design Quality Engineer

As a Design Quality Engineer, you will work closely with R&D to ensure product quality and product safety. You will be part of a global team within the CT organization and will drive quality initiatives across the global business.

You will work within the Quality Management System and actively contribute to its continuous improvement.

Please apply in English.

Your role:

  • Coordinating and supporting quality activities while ensuring compliance with regulatory requirements, patient safety, and product quality throughout the entire product lifecycle.
  • Proactively supporting development teams during the development process, both for new product introductions and lifecycle management, while providing independent quality assessments.
  • Supporting risk analyses and maintaining risk management documentation through objective and independent evaluations.
  • Coordinating product safety certifications in collaboration with testing and integration teams and managing interactions with external certification bodies.
  • Actively supporting external and internal audits and implementing resulting improvement measures.

The position offers:

  • A broad variety of tasks through continuously evolving technical challenges.
  • A high degree of ownership, autonomy, and decision-making responsibility.
  • The opportunity to implement new regulatory requirements in practical development projects while collaborating with stakeholders across multiple functions.

You're the right fit if you have:

  • Bachelor's Degree in Mechanical Engineering, Electronics Engineering, Science or equivalent/ Vocational Education.
  • Basic knowledge of the regulatory framework and requirements applicable to medical devices.
  • Knowledge of electrical engineering, preferably including high-voltage technology.
  • Experience with risk management and medical device safety requirements.
  • Strong analytical thinking and problem-solving skills, with the ability to build convincing arguments.
  • Curiosity and motivation to explore, use, and further develop AI tools to support daily work.
  • Fluent English and German (please apply in English)

We believe that we are better together than apart. For this role, it means working in-person at least 3 days per week. 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 the lives of others.

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