Quality Engineer - Medtech 80-100%

• 06 July 2026 • 100% • Indeterminate duration • Murten Our client operates in a regulated environment with high quality requirements. This position will allow you to have a concrete impact, with responsibilities, influence and visible results. CDI - Rate 80-100% Quality Engineer - Medtech 80-100% • Higher technical education (HF/HES), completed by a specialization in quality management • Several years of experience in quality assurance in a production environment, ideally in medical devices according to ISO 13485 • Good knowledge of Lean Management • Excellent communication skills with internal and external stakeholders • Good mastery of MS Office as well as experience with CAQ and ERP systems • Languages: French, German (C1), English (B2) We offer • A position with responsibilities and direct influence on quality processes and visible results • A demanding, stimulating and continuous improvement-oriented environment • An open culture • 6 weeks of vacation • Attractive employee benefits • Ensure compliance with the highest quality standards and promote a sustainable quality culture in a regulated environment (GxP, ISO 13485, FDA 21 CFR Part 820) • Manage changes, deviations and 8D reports, and drive effective corrective and preventive actions (CAPA) • Plan and accompany internal and external audits (customers, authorities and suppliers) as a reference person • Coordinate and drive process qualifications and validations (IQ/OQ/PQ), and ensure their implementation • Ensure the release of batches and ensure that only compliant products continue the process • Actively contribute to the continuous improvement of quality processes through Lean methods and an efficiency- and impact-oriented approach • Participate in the development of the certified quality management system and bring your ideas in accordance with ISO 13485 and FDA requirements