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