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Lüneburg

    Specialist Process Validation - Lüneburg, Deutschland - Vality One Recruitment GmbH

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    Employee
    Beschreibung

    Dein Aufgabengebiet

    • Vorbereitung, Durchführung und Dokumentation der Prozessvalidierungen
    • Erstellung und Erläuterung von Validierungskonzepten
    • Durchführung von Risikobewertungen und Ableitung von Maßnahmen
    • Bearbeitung von Abweichungen, Root Cause Analysen und CAPAs
    • Erstellung von GMP-konformer Dokumentation und Schulung von Mitarbeitern
    • Teilnahme an Audits und Inspektionen
    • Schnittstellenmanagement (intern und extern)

    Dein Hintergrund

    • Abgeschlossenes naturwissenschaftliches Studium (Biologie, Pharmazie, Chemie, Lebensmitteltechnik, Pharmatechnik o.ä.)
    • Berufserfahrung im Bereich der Validierung in einem pharmazeutischen Unternehmen
    • Fundierte Kenntnisse der GMP Regularien
    • Idealerweise Erfahrung mit CSV und SAP
    • Überzeugungskraft, Dienstleistungsorientierung, Engagement und Flexibilität
    • Sehr gutes Kommunikations- und Organisationsgeschick
    • Fließende Deutsch- und Englischkenntnisse in Wort und Schrift

    Deine Benefits

    • Attraktive Vergütung inklusive Weihnachtsgeld
    • Hochmodernes und internationales Arbeitsumfeld
    • Betriebliche Altersvorsorge & Gesundheitsmanagement
    • Flexible Arbeitszeiten
    • Möglichkeit zum mobilen Arbeiten
    • Mitarbeiterrestaurant
    • Mitarbeiterrabatte und Einkaufsvorteile
    • Internationale Karriere- und Weiterbildungsmöglichkeiten

    Gender-Hinweis

    Aus Gründen der besseren Lesbarkeit
    wird auf die gleichzeitige Verwendung
    der Sprachformen männlich, weiblich
    und divers (m/w/d) verzichtet.
    Sämtliche Personenbezeichnungen
    gelten gleichermaßen für alle
    Geschlechter.



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