Quality Manager - Medtech - ALL / ANG / FR
- Employment type
- Full-time
- Location
- Neuchâtel
- First posted
- 03 août 2026
- 100%
- Durée indéterminée
- Neuchâtel
Mandated by one of our clients, we are looking for a:
Quality Manager - Medtech - ALL / ANG / FR
- Higher technical education (ES/HES), completed by training in quality management
- Proven experience in quality assurance in a Medtech production environment
- Experience in team management and a strong interest in technical subjects
- Good knowledge of ISO 13485, FDA 21 CFR Part 820, CAPA, audits and change management
- Experience in Regulatory Affairs = an asset
- Training or good knowledge in Lean Management
- Confident communication with internal departments, clients and suppliers
- Good proficiency in MS Office, CAQ/ERP experience
- Languages: French and German = fluent; English = good level
The advantages:
- A key position with global quality responsibility across two sites
- An international Medtech environment, demanding and oriented towards continuous improvement
- An open culture, rapid decisions and an open-door philosophy
- Opportunities for individual development
- 6 weeks of vacation, attractive social benefits, team events and loyalty bonuses
Our client, an international company active in the development and manufacture of solutions for medical technologies, is looking for a Quality Manager for two sites in Suisse romande. You will play a key role in steering the quality system, managing the QA team and continuous improvement.
- Fulfill the function of Quality Management Representative for the certified and harmonized QMS on 2 sites
- Manage the QA team of the two sites and guarantee the global responsibility for local quality activities
- Maintain and improve the QMS according to ISO 13485, FDA 21 CFR Part 820 and applicable regulations
- Drive internal, client and notified body audits, from preparation to follow-up of actions
- Be the main interlocutor for clients, authorities, notified bodies and partners on quality subjects
- Supervise key QA processes: complaints, CAPA, change management and audit management
- Monitor quality KPIs, report QMS performance to management / Global QA and drive continuous improvement
- Manage QA resources, team leadership and the budget
- Support Regulatory Affairs activities
Automatically translated from the original.
Posted 5 weeks ago