Quality Engineer

Be part of a collaborative and professional workplace where you can make a meaningful impact on patient lives globally, contributing to audits, projects, and continuous improvement initiatives with a real influence on quality outcomes.

Our Team

As part of our Quality Team in Struer, you will work across projects and daily operations to ensure compliance, support manufacturing, and drive continuous improvement within a regulated medical device environment.

What You Will Do

• Support the setup, planning, and introduction of new products into production in collaboration with development teams
• Perform batch release activities in compliance with regulatory requirements and our Quality Management System
• Support manufacturing by ensuring effective in-process, incoming, and outgoing quality control
• Implement customer-specific quality requirements within production processes
• Identify and implement process improvements, including optimisation within SAP
• Drive deviations and CAPAs in collaboration with cross-functional teams
• Partner with customers to review quality agreements and participate in regular quality and project discussions
• Contribute to continuous improvement initiatives to enhance compliance, efficiency, and product quality outcomes

Who You Are (Basic Qualifications)

• Bachelor’s degree in engineering or a related field
• Understanding of product development processes and quality requirements
• Strong knowledge of quality documentation standards and compliance practices
• Ability to collaborate effectively across functions in a professional environment
• Proactive mindset with the ability to identify and drive improvement opportunities
• Strong communication skills in English
• Experience working with SAP and MS Office

What Will Put You Ahead

• Knowledge of ISO 13485
• Experience with Quality Management Systems and good documentation practices
• Experience in assembly, or cleanroom production environments
• Audit experience