Quality Assurance Coordinator

Philips UK

Zaventem, , Belgium
Quality management system
Iso 13485 compliance
Fda 21 cfr 820 compliance
Support international quality operations and transformation initiatives, ensuring compliance, continuous improvement, and product excellence in a regulated medical device environment

Job Summary

  • Support international quality operations and transformation initiatives, ensuring compliance, continuous improvement, and product excellence in a regulated medical device environment.
  • Provide Quality Assurance support for international transformation projects, including quality transition planning, intra-company quality agreements, and change control activities.
  • Collaborate with cross-functional and international stakeholders to ensure consistent and streamlined quality processes across sites.

Matching Summary

Support international quality operations and transformation initiatives, ensuring compliance, continuous improvement, and product excellence in a regulated medical device environment.

Skills & Requirements

Must-have

  • Quality Management System
  • ISO 13485 compliance
  • FDA 21 CFR 820 compliance
  • EU MDR 2017/745 compliance
  • nonconformance management
  • root cause analysis
  • CAPA execution

Nice-to-have

  • dynamic and confident
  • approachable
  • cross-functional collaboration
  • continuous improvement mindset

Key Requirements

  • Degree in science or engineering
  • Relevant working experience in Quality
  • Experience in regulated industry
  • Experience in medical device industry
  • Fluent in English

Work Rights

Not specified

Tailored Resume

Cover Letter