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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


  • 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

Tagged as: qa jobs

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