-Oversight of all production & testing activities, ensures compliance with cGxP, incl. data integrity and eCompliance -Support exception investigations -Review and approval of production, QC, and AS & T records -MBR review -Support OpEx improvement projects Qualified Person – Executes batch release in compliance with registration
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Lab Supervisor , Sasayama
Novartis Pharma K.K. 13日前
Associate, Investigation Expert,Sasayama
Novartis Pharma K.K. 13日前
Associate, CRA
Novartis Pharma K.K. 13日前

External Supply Quality Assurance Manage

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