Quality Expert R&D and Global Engineering
vor 1 Woche
Deine Aufgaben:
- Sicherstellung der Pflege und Weiterentwicklung des R&D Quality Management Systems (QMS) gemäss Industriestandards
- Überwachung des R&D CAPA-Prozesses und Durchführung interner Audits nach ISO 15378 und ISO 13485
- Vorantreiben kontinuierlicher Verbesserungsinitiativen innerhalb von R&D und Sicherstellung einer nahtlosen Compliance in der Entwicklungsdokumentation
- Schulung und Unterstützung von Kolleginnen und Kollegen, um eine effiziente Einhaltung der QMS-Standards zu ermöglichen
- Abgeschlossenes Studium in Ingenieurwissenschaften, Life Sciences oder einem verwandten Bereich
- Mindestens 3 Jahre Berufserfahrung in der pharmazeutischen Verpackungs-, Medizinprodukt- oder Pharmabranche, idealerweise im Entwicklungsumfeld mit Bezug zu QMS-Standards
- Fundierte Kenntnisse im Bereich QMS, Dokumentenmanagement und Good Documentation Practice (GDocP)
- Ausgeprägte Präsentations- und Moderationsfähigkeiten sowie eine hohe Genauigkeit und Sorgfalt
- Erfahrung in der Teilnahme oder Leitung von Audits; ISO 13485 / ISO 15378 Auditor-Zertifizierung von Vorteil
- Hervorragende Kommunikationsfähigkeiten in Deutsch und Englisch und Freude am Austausch mit internen und externen Stakeholdern
- Flexible Arbeitszeiten
- Hauseigene Kantine
- Vorteilhafte, private und berufliche Versicherungslösungen
- Anzahlung an Halbtax / GA
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