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Process Validation Specialist

vor 3 Monaten

Berlin, Berlin, Deutschland NextPharma Vollzeit
Process Validation Specialist (m/w/d) Standort:

Berlin, BE, DE,

Berufsfunktion: Entwicklung Startdatum: ab sofort Arbeitszeit: Vollzeit Sie suchen...

nach einer spannenden beruflichen Herausforderung? Wir sind einer der führenden, europäischen Auftragshersteller im Bereich der Pharmazeutischen, Biotech- und Health Care-Industrie mit rund 2.200 Kolleginnen und Kollegen in Deutschland, Frankreich, England, Finnland und Norwegen. Für uns ist der wichtigste Schritt immer der Nächste. Denn Schnelligkeit treibt uns an, erfüllt unsere Arbeitswelt mit Dynamik und lässt uns wachsen. Unser bestes Rezept für gemeinsamen Erfolg: Raum für Passion. Denn wir sind uns sicher: Wo exzellenter Service weltweit begeistert, ist Leidenschaft die beste Medizin. Willkommen in der Arbeitswelt von NextPharma.

Zur Verstärkung unseres NextPharma Teams in Berlin suchen wir ab sofort eine/n:

Process Validation Specialist (m/w/d)

Was sind die Aufgaben dieser Stelle?

  • Planung von Validierungsvorhaben zur Optimierung von bestehenden Prozessen und zur Etablierung von neuen Produkten
  • Erarbeitung von Validierungskonzepten
  • Erstellung von Risikobewertungen zum Prozess (FMEAs), Validierungs- und Musterzugsplänen
  • Begleitung von Prozessvalidierungen in der Pharmaproduktion
  • Auswertung der Ergebnisse sowie Erstellung von Validierungsreports
  • Abteilungsübergreifendes Projektmanagement von Validierungsprojekten am Standort
  • Aufrechterhaltung des validierten Zustandes von Produkten in der Routineproduktion

Was bieten wir Ihnen?

  • Passgenaues On-Boarding
  • Mobiles Arbeiten, eine flexible Arbeitszeitgestaltung und 30 Urlaubstage
  • Betriebliche Altersvorsorge
  • Mitarbeiter-Events und betrieblicher Sport
  • Weiterbildungen bei der internen NextAcademy
  • Interne Weiterentwicklungen und standortübergreifende Karrieremöglichkeiten
  • Mitarbeiter-Rabatte

Was sollten Sie mitbringen?

  • Abgeschlossenes Studium im Pharmabereich z.B. Pharmazie, Pharmaingenieurswesen oder Pharmatechnik
  • Erfahrung mit der Herstellung fester Arzneiformen
  • Berufserfahrung in der Pharmaindustrie wünschenswert
  • Kenntnisse einschlägiger GMP Guidelines EU und FDA
  • Ausgeprägte Kommunikations- und Organisationsfähigkeit, sowie sehr hohes Maß an Zuverlässigkeit und Qualitätsbewusstsein
  • Kompetenter Umgang mit Microsoft Office Anwendungen
  • Sehr gute Deutsch- und Englischkenntnisse
It's time for your next chapter:

Wir freuen uns auf Ihre Bewerbung.

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