Quality Engineer - Medtech 80-100%

Location Neuchâtel Availability Immediately Type Fixed Reference 41270 Published on 08/07/2026 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% Job Description ### • 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 modifications, deviations, and 8D reports, and drive effective corrective and preventive actions (CAPA) • Plan and accompany internal and external audits (clients, authorities, and suppliers) as a reference person • Coordinate and drive process qualifications and validations (IQ/OQ/PQ), and ensure their implementation • Ensure batch release and ensure that only compliant products continue the process • Contribute actively to the continuous improvement of quality processes using Lean methods and an efficiency- and impact-oriented approach • Participate in the development of the certified quality management system and provide your ideas in accordance with ISO 13485 and FDA requirements Profile ### • 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 environment focused on continuous improvement • An open culture • 6 weeks of vacation • Attractive employee benefits Quality Engineer - Medtech 80-100% / Fixed