Quality Assurance Engineer

Quality Engineering at This AG - A Rayner Group Company plays a crucial role in delivering high quality and high performance medical devices to people around the world. It ensures our quality standards are rigorous and robust processes, built into manufacturing at every step from raw material inspection to final product release. Through continuous improvement and teamwork we continue to excel and meet this goal together.

We’re seeking a Quality Assurance Engineer who thrives on collaboration and precision. In this role, you will play a key part in ensuring the highest standards across our processes, working closely with cross‑functional teams to drive continuous improvement and deliver exceptional results.

Please note this role is 100% on-site at our THIS AG HQ in Heerbrugg, Switzerland.

• Initiate and lead CAPA investigations with cross‑functional teams including Production and Process Engineering to deliver defect reduction
• Development, implementation and continual review of quality controls in QA and Production departments. Includes receiving inspection processes, in‑line manufacturing processes and product release
• Manage non‑conformity and supplier activities to ensure compliance and improve performance
• Support new product and process development projects and ensure compliance with applicable regulations
• Drive process and continuous improvement in Manufacturing to improve quality and efficiency of receiving inspection and in‑line process checks
• Build effective working relationships with colleagues and suppliers
• Monitor, trend and report on quality performance data to track KPIs
• Actively promote a Quality culture within Rayner and throughout the supply chain

• Proven track record of process improvement experience resulting in better quality, cost, efficiency and time within a manufacturing environment
• Degree, equivalent qualification, or equivalent industrial experience in a science, clinical or engineering background
• 2-3 years’ experience in a Quality Engineering role
• Experience with Quality System concepts, practices and procedures
• Experience working in a high volume, fast‑paced manufacturing setting
• Working knowledge of standards such as cGMP, FDA 21 CFR Part 820 QSR and ISO 13485 Medical Device Quality Management Systems

• Global appreciation platform to recognise colleagues around the globe
• Fantastic opportunity to work with highly talented teams and individuals and grow with the business
• Being part of an organisation you can be proud to work for changing the lives of millions of people!