12.06.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalPerson Delegate. How you will contribute - Ensures the day-to-day quality oversight of the Quality Control activities and Raw Material management related to his/her scope of responsibility - Ensures raw material release and manages specifications - Collaborates with suppliers to address quality issues
Später ansehen12.06.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalManufactured in Neuchâtel (clinical phase III and commercial). - Manage/prepare the necessary supportive documentation for regulatory submissions and for major change projects in Neuchâtel facility. - Prepare/Review documentation for change controls, audit observations and regulatory agency questions
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