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Full-Time Opportunity: This is a permanent, full-time position with a competitive package and real career growth potential.
Job Description
Main tasks
- Responsible for the batch record review process and further development of the system
- Support in the further development of the deviation management system, as well as the investigation and CAPA system
- Support in the creation of the PQR / APR
- Representative of QA “on the shop floor” in various areas (e.g. production, laboratory)
- Support the area if necessary, especially with quality oversight
Qualifications
- Studies or initial professional experience in the pharmaceutical industry or other comparable experience in the industrial or pharmaceutical sector
- GMP knowledge
- Knowledge of qualification/validation of aseptic manufacturing processes
- Very good MS Office knowledge
- Fluent in German and good knowledge of English
- Ability to grasp connections quickly, work under pressure and strive for continuous improvement
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