Hands-On Quality Engineer – 6-Month Contract, Potential FTE

headcount | recruitment driven by science

Zug

Vor Ort

CHF 90.000 - 120.000

Teilzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

Eine maßgeschneiderte Bewerbung für diese Stelle — ein maßgeschneiderter Lebenslauf und ein Anschreiben, die genau zur Stellenanzeige passen.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

headcount is seeking a hands-on Quality Engineer in Zurich to collaborate with Production and Manufacturing. The role focuses on on-floor quality issues and ensuring effective resolutions within a regulated medical device environment.

The candidate will own CAPAs and NCs, perform root-cause analyses, and support change controls and process improvements while ensuring ISO 13485 compliance.

Qualifikationen

  • 3+ years of Quality Engineering in medical devices.
  • Hands-on CAPA, NCs and root-cause investigations.
  • Experience in a production/manufacturing environment.
  • Knowledge of ISO 13485 and QMS.
  • Experience with risk management, change control or process validation.
  • German fluent and good English.

Aufgaben

  • Own and manage CAPAs, non-conformances (NCs) and deviation investigations.
  • Perform root-cause analysis and implement corrective/preventive actions.
  • Provide hands-on Quality Engineering support on the production floor.
  • Support change controls, risk assessments and process improvements.
  • Review and disposition non-conforming materials/products.
  • Work closely with Production, Manufacturing Engineering and Operations.
  • Support process validation/qualification and audit activities.
  • Ensure compliance with ISO 13485 and internal QMS requirements.

Kenntnisse

CAPA management
Root-cause analysis
Production floor
ISO 13485
QMS knowledge
Risk management
Change control
Process validation
German fluent
English good

Jobbeschreibung

headcount is seeking a hands-on Quality Engineer in Zurich to collaborate with Production and Manufacturing. The role focuses on on-floor quality issues and ensuring effective resolutions within a regulated medical device environment.

The candidate will own CAPAs and NCs, perform root-cause analyses, and support change controls and process improvements while ensuring ISO 13485 compliance.

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