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Responsible for the GRA QMS, including implementation of QMS strategy and tactics
Responsible for supporting and coordinating GRA internal Policy / SOP / WI creation, review, approval, version control and ensuring consistency across
QA oversight of documentation management processes with respect to fulfill authority guidelines and Novartis/Sandoz standards
QA contact person for the implementation of the new Novartis documentation management IT system D4N
Quality assurance tasks with focus on activities regarding medical devices
Support in quality topics, e.g. deviations, complaints, CAPAs
Support in QA Lab for investigation of samples
Participation in the release process of medical...
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