Specialist Qualification
Vor 3 Tagen
Ihr Aufgabengebiet
- Erstellung von Qualifizierungsdokumentation und Protokollen
- Erstellung und Anpassung von SOPs
- Administration von Dokumenten betreffend Qualitätsmanagement
- Unterstützung bei der Einhaltung der GMP Regularien
- Koordination der Qualifizierungsaktivitäten (u.a. Planung und Koordination)
- Enge Zusammenarbeit mit dem Projektmanagement
Ihr Hintergrund
- Studium der Naturwissenschaftenoder eine vergleichbare Ausbildung mit Zusatzqualifikation
- Idealerweise erste Berufserfahrungen in der pharmazeutischen Industrie
- Sicherer Umgang mit gängigen MS Office Anwendungen
- Selbstständige Arbeitsweise, proaktiver Teamplayer
- Kommunikative und zielorientierte Persönlichkeit
Ihre Benefits
- Spannende Herausforderungen in einem zukunftsträchtigen und wachsenden Unternehmen
- Eine offene Arbeitsatmosphäre in einer offenen Unternehmenskultur mit kurzen Kommunikationswegen
- Ein attraktives Vergütungspaket sowie interessante Weiterentwicklungsmöglichkeiten
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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