Quality Assurance Coordinator

As a Quality Assurance Coordinator, you support international quality operations and transformation initiatives, ensuring compliance, continuous improvement, and product excellence in a regulated medical device environment. This role involves providing QA support for transformation projects, daily QA operations, audit preparation, nonconformance management, and QMS implementation and improvement. The position is a 1-year contract.

Must Have

• Provide Quality Assurance support for international transformation projects
• Support daily Quality Assurance operations
• Support preparation and follow-up for internal and external audits
• Execute and verify quality assurance activities
• Support nonconformance management, root cause analysis, and CAPA execution
• Support the implementation, maintenance, and continuous improvement of the Quality Management System
• Contribute to process improvements, SOP/WI updates, and quality awareness initiatives
• Collaborate with cross-functional and international stakeholders
• Degree in science or engineering
• Relevant working experience in Quality in the regulated industry, ideally in the medical device industry
• Fluent in English

Good to Have

• Experience in supply chain quality
• Any other language is an advantage

Quality Assurance Coordinator As a Quality Assurance Coordinator, you support international quality operations and transformation initiatives, ensuring compliance, continuous improvement, and product excellence in a regulated medical device environment. We offer 1 year contract. ### Your role: * Provide Quality Assurance support for international transformation projects, including quality transition planning, intra-company quality agreements, and change control activities. * Support daily Quality Assurance operations such as system installation quality reviews, returned material assessments, inspection documentation review, and correction & removal activities. * Support preparation and follow-up for internal and external audits. * Execute and verify quality assurance activities in line with established procedures and regulatory requirements. * Support nonconformance management, including NCR review and approval, root cause analysis, and CAPA execution within defined timelines. * Support the implementation, maintenance, and continuous improvement of the Quality Management System in accordance with ISO 13485, FDA 21 CFR 820, and EU MDR 2017/745. * Contribute to process improvements, SOP/WI updates, and quality awareness initiatives across the organization. * Collaborate with cross-functional and international stakeholders to ensure consistent and streamlined quality processes across sites. You’re the right fit if: * Degree in science or engineering * Relevant working experience in Quality in the regulated industry, ideally in the medical device industry * Experience in supply chain quality is a plus * Dynamic, confident, approachable * Fluent in English, any other language is an advantage How we work together We believe that we are better together than apart. For this role, this means working in-person at least 3 days per week. About Philips 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. * Learn more about our business. * Discover our rich and exciting history. * Learn more about our purpose. If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care here.