Technical Author R&D (a), 100%
About this role
Technical Author R&D (a), 100% for writing production-relevant GMP documents
You work gladly in a GMP-regulated environment and enjoy creating the corresponding documents. You can quickly familiarize yourself with changing tasks and show flexibility in prioritizing your work. Through your strong communication skills and structured and precise work method, you coordinate and process cross-departmental tasks successfully. You strive to complete assignments on time independently or in a team, ensuring a delay-free production flow.
Ihre Aufgaben:
- Sie erstellen, überprüfen und aktualisieren Dokumente wie Herstellvorschriften, SOPs, Prozessvalidierungspläne und -berichte für unsere Wirkstoffproduktion. Dabei arbeiten Sie eng mit den entsprechenden Produktionsabteilungen zusammen
- Sie implementieren Prozessoptimierungen hinsichtlich Qualitäts- und Effizienzsteigerung
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