Quality Manager

For our client, an innovative company that develops, manufactures, and markets medical devices for therapeutic applications worldwide, we are looking for a

Quality Manager (80% - 100%)
Location: Neuchâtel, NE
Start date: Beginning of 2026

Your responsibilities.

• Drive the continuous development and implementation of the QMS in compliance with ISO 13485, MDR, and MDSAP.
• Act as the official Deputy to the Quality Management Representative & PRRC.
• Lead and manage key QMS processes, including Management Reviews, CAPA, Risk Management, and Change Management.
• Take main responsibility for establishing and updating all compliant technical documentation.
• Manage the complete market access registration process for worldwide distribution.
• Oversee and conduct supplier quality management activities.
• Conduct internal audits as per the audit program and support the company during external audits and inspections (Notified Bodies, Competent Authorities).
• Provide dedicated Quality Management support to various projects.
• Monitor regulatory and standard changes, informing management of their impact.
• Maintain the Document Management System and supervise the quality of product realization records.

Your profile

• A minimum of 2 years of experience in a similar Quality Management role within the medical device industry (industrial production).
• Proven experience with international regulatory affairs and risk management.
• Strong, practical knowledge of the core medical device standards and regulations: ISO 13485, MDR, and MDSAP.
• Fluency in both English (written and spoken) is mandatory.
• Proficiency in French and/or German is a strong asset.