Category

Description

Main Responsibilities:

Support and manage corporate Quality Control (QC) - and if needed Quality Assurance (QA) business process harmonisation and improvement activities
Support the strategy for implementation of a paperless laboratory
Lead a program to define, implement and review global data governance standards for global QC applications
Lead a program to define, implement and review global data integrity standards for global QC applications (considering aspects like audit trail review, user management review and global data review)
Lead and support the development, validation, implementation and maintenance of corporat IT-Systems used in QC and ensure that key user support as well as training is provided as required
Support the integration into the global IT landscape SAP, MES and PLM (MDM)
Trouble shooting and management of IT-System incidents, issues and changes, if necessary routing issues to other internal or external partners
Write, review or approve related manuals and procedures
Provide input during the global Quality audit planning cycles and execute internal and external Quality audits according to plan
Support the development, implementation and maintenance of the Vifor Pharma Quality System
Provide input for the Quality KPI Report and implement performance improvements
Supervise the CQM Application Manager for QC IT Systems as direct line manager
Support agency inspections and customer audits as needed
Provide input and controlling of budget

Qualifications and Experience:

Higher degree (Bachelor or Master) in a natural science field
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