Contract duration: 31.12.2025
Responsibilities:
* CAPA and NC ownership and investigation documentation
* Audit front room support
* Quality database support (COMET) Keeps track on due dates and writes investigation reports with a best-in-class quality.
* Work in close collaboration with department manager on timeline & deliverables.
* Managing and shaping internal processes.
* Close cooperation with internal departments.
* Create impact assessments, investigation reports and risk files.
* Create storylines for audit front rooms.
* Working with engineers and equipment owners as well as external providers to be compliant within our processes.
* Support manufacturing plant excellence at the site by providing guidance.
Requirements:
* Preferably master diploma (preferably mechanical, electrical, industrial, chemical) or equivalent
* Fluent German and English
* Min. 5 years of experience in GMP quality systems preferably in Pharma industry
* Audit front room experience
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