QA Manager
vor 2 Wochen
In Zusammenarbeit mit den CSV Validierungs-Teams und/oder den Equipment Qualifizierungs-Teams:
- Beratung bei der Erstellung der CSV Validierungspläne und/oder Qualifizierungspläne.
- Freigabe der Pläne und Berichte, sowie aller weiteren relevanten Dokumenten.
- Freigabe von GxP Changes oder Abweichungen gemäss globalen Prozessen
- Genaue Impact-Analyse auf lokale Prozesse bei Änderungen im globalen Qualitätsmanagement-System
- Vorbereitung und Abdeckung von QA-Aspekten in ISO13485 Audits
Ihr Hintergrund:
- Abgeschlossenes Studium in einem technischen oder naturwissenschaftlichen Bereich
- 3 Jahre CSV Validierungserfahrung im Medtech Bereich (ISO und/oder Erfahrung im Bereich Equipment Qualifizierung/Management und Kalibrierung im Zusammenspiel mit starker Lernfähigkeit
- Erfahrung im Bereich Qualitätssicherung ist ein Vorteil
- Starke Persönlichkeit, die sich argumentativ durchsetzen kann
- Sehr gute Deutsch- und Englischkenntnisse sind erforderlich
Does this job fit your talents and seem right for you? Don't hesitate to apply online now.
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