Sr Document Control Administrator
vor 7 Monaten
Aufgabenbereich:
- Überprüfung der GxP Chargenprotokolle inklusive der Freigabe auf Herstellungsebene
- Zusammenarbeit mit den Kollegen aus verschiedenen Bereichen, um sicherzustellen, dass die oben genannten Dokumente den Kunden
- und behördlichen Anforderungen entsprechen
- Koordination und interne Kommunikation bezüglich der Terminierung und Fertigstellung der Dokumentation
- Unterstützung bei der Verbesserung der Dokumentationskennzahlen (Right First Time Metrics)
- Sicherstellung, dass alle Abweichungen oder Qualitätsprobleme gemäss GxP dokumentiert werden
- Schulung und Einführung neuer Teammitglieder, einschließlich Zeitarbeitskräften, falls erforderlich
Qualifikation:
- Erfahrung in der pharmazeutischen Industrie, pharmazeutische Produktion/Verpackung, Qualitätskontrolle/Qualitätssicherung,
- Erfahrung in Umgang mit Medikamenten im wissenschaftlicher Bereich oder gleichwertig
- Gute Microsoft Kenntnisse (Excel, Word etc.)
- Erfahrung oder GxP-Ausbildung
- Bachelor-Abschluss in Naturwissenschaften, oder 3-5 Jahre Berufserfahrung in der GMP-Produktion
- Ausgezeichnete Kommunikations
- und Organisationsfähigkeiten
Sehr gute Kenntnisse der deutschen Sprache und gute Kenntnisse der englischen Sprache
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