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Quality Manager - Medtech - ALL / ANG / FR

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Employment type
Full-time
Location
Neuchâtel
First posted
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  • 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

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