Quality Manager - Medtech - ALL / ANG / FR

• 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