Quality Engineer - MedTech - ALL / ANG / FR

Location Neuchâtel Availability Immediately Type Fixed Reference 41289 Published on 09/07/2026 Mandated by one of our clients, we are looking for a: 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 • Take charge of change management, deviations, and 8D reports, and drive effective corrective and preventive measures: CAPA • Plan and accompany internal and external audits (clients, authorities, and suppliers) and intervene as the main contact person • Coordinate and drive process qualifications and validations: IQ/OQ/PQ, and ensure their proper implementation • Be in charge of batch release and ensure that only compliant products continue the process • Contribute actively to the continuous improvement of quality processes using Lean methods • Participate in the development of the certified quality management system and provide own ideas, in compliance with ISO 13485 and FDA requirements Profile ### • Higher technical education in Mechanics (or equivalent), completed by a training in quality management • Several years of experience in quality assurance in a production environment (ISO 13485) • Knowledge of Lean Management = an asset • Excellent communication skills with internal and external stakeholders • Very good mastery of MS Office and experience with CAQ and ERP systems • Languages: German = mother tongue, very good knowledge of English and French The benefits: • Join a modern and dynamic company • A stimulating technical environment, in contact with high-value-added products • Good conditions Quality Engineer - MedTech - ALL / ANG / FR / Fixed