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