27.04.24 | Vollzeit | Allschwil | Thermo Fisher ScientificResponsibilities Review of executed batch records, creation of certificate of packaging Support QA Pre-Approval as required by line manager/workload Review and quality approval of pre-executed batch documentation, finished product with TOE and label components, change orders, packaging and labelling requests
Später ansehen18.04.24 | Vollzeit | Oberdorf (BL) | Randstad Schweiz AGAnd Internal Audit (IA) Observations. - Support site Document Control and Records Information Management activities. - Support the coordination, preparation, facilitation, execution, and tracking of activities of the Quality Progress Review (QPR), Quality System Management Review (QSMR), and other KPI metrics
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