Quality Engineer - MedTech - ALL / ANG / FR

Location Neuchâtel Availability Immediately Type Permanent Reference 41490 Published on 18/07/2026 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 as well as 8D reports, and lead effective corrective and preventive measures: CAPA • Plan and support internal and external audits (clients, authorities and suppliers) and act as the main interlocutor • Coordinate and lead qualifications as well as process validations: IQ/OQ/PQ, and ensure their proper implementation • Be in charge of batch release and ensure that only compliant products continue the process • Actively contribute to the continuous improvement of quality processes, using Lean methods • Participate in the development of the certified quality management system and contribute own ideas, in compliance with ISO 13485 and FDA requirements Profile ### • Higher technical education in Mechanics (or equivalent), completed by 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 interlocutors • Very good mastery of MS Office as well as experience with CAQ and ERP systems • Languages: German = native language, very good knowledge of English and French Advantages: • 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 / Permanent