Validation Specialist
vor 2 Wochen
**Unser Angebot**:
- Spannende, selbstorganisierte und eigenverantwortliche Aufgaben
- Langfristiges Arbeitsverhältnis, angenehmes Betriebsklima in einem jungen, engagierten Team
- Gleitzeitvereinbarung, flexibles Arbeitszeitmodell, Work-Life-Balance
- Spezialisierungsmöglichkeiten sowie fachspezifische Weiterbildungen und Trainings
- Ausgesprochen kollegiales Team mit freundschaftlicher Umgangsweise
- Vielfältige Entwicklungsmöglichkeiten innerhalb der Capgemini Engineering Group
**Ihre Aufgaben**:
- Du bist für die Durchführung und Koordination von Qualifizierungs
- und Validierungsaktivitäten gemäß der gültigen GMP Anforderungen zuständig
- Du erstellst phasenspezifische Testpläne und Berichte (IQ, OQ, PQ und DQ)
- Du übernimmst die Organisation, Moderation und Dokumentation von Risikoanalysen (FMEA, HACCP)
- Du wirkst als Projektschnittstelle zwischen den Fachabteilungen Produktion, Quality Assurance, Lieferant und verantwortlicher Nutzer
- Du bietest fachliche Unterstützung bei der Angebotserstellung
- Du nimmst an Gesprächen im Rahmen der Kundenakquisition teil
**Ihr Profil**:
- Abgeschlossene Ausbildung (TU, FH, HTL) in einer technischen oder naturwissenschaftlichen Fachrichtung (zB Pharmazie, Chemie, Verfahrenstechnik oder vergleichbar)
- Berufserfahrung in der pharmazeutischen Industrie oder Beratungserfahrung im GMP-regulierten Umfeld notwendig
- Erfahrung im Bereich CS-Validierung und Projektmanagementkenntnisse von Vorteil
- Kenntnisse der aktuellen GMP Vorgaben
- Bereitschaft zur Reisetätigkeit
- Verhandlungssichere Deutsch
- und Englischkenntnisse
Das Bruttojahresgehalt beträgt mindestens EUR 50.000€, selbstverständlich bieten wir jedoch eine marktkonforme Überbezahlung in Abhängigkeit von der Qualifikation und Berufserfahrung.
Wir freuen uns auf deine Online Bewerbung
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