Stv. Quality Director
Vor 3 Tagen
Unser Kunde
Unser Kunde ist ein traditionsreiches Unternehmen, das sich auf die Herstellung und Abfüllung von chemisch-pharmazeutischen Produkten spezialisiert hat. Das Unternehmen mit Standorten in Deutschland und der Schweiz ist von der Formulierung, über die Produktion bis zur Abfüllung und Logistik in allen Bereichen tätig. Arbeitsort: Schötz
Aufgaben
- Stellvertretung der FvP und der Leitung Quality
- Verantwortung für alle qualitätsrelevanten Themen in der Produktion und Konfektionierung
- Review und die Freigabe von Qualifizierungs
- und Validierungsdokumenten
- Bearbeiten Abweichungen, Changes und CAPAs
- Review und Freigabe von Batch Records und Erstellen der APR/PQR
- Begleitung von Behördenaudits (national und international)
- Vertreten der Quality-Abteilung gegenüber internen und externen Ansprechpartnern
Qualifikation
- Abgeschlossenes naturwissenschaftliches Studium (Chemie, Pharmazie, Biologie) oder ähnliches. Eine Weiterbildung im Qualitätsmanagement ist von Vorteil
- Mindestens 3-5 Jahre Berufserfahrung in der Qualitätssicherung im GMP und/oder ISO13485 regulierten Umfelds
- Know-how in einem produzierenden pharmazeutischen Unternehmen mit flüssigen, halb-festen oder festen Arzneiformen ist ein grosses Plus.
- Offene, kommunikative Persönlichkeit mit hands-on Mentalität
- Sehr gute Organisationsfähigkeiten, Flexibilität und vernetztes Denken zeichnen Sie aus
- Gute Deutsch
- und Englisch-Kenntnisse in Wort und Schrift
**Benefits**:
- Sehr gute Einarbeitungszeit mit spannenden Entwicklungsperspektiven
- Zeitgemässe Anstellungsbedingungen
- Vielseitiges und abwechslungsreiches Aufgabengebiet mit viel Eigenverantwortung
Wenn Sie an dieser spannenden Herausforderung interessiert sind, bewerben Sie sich online bei Herr Kelaja Wick. Auf unserer Homepage finden Sie auch weitere spannende Stellen und mehr Informationen zum Bewerbungsablauf. Wir freuen uns, Sie bald persönlich kennen zu lernen. Diskretion ist unser Kapital.
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