Background:
You will be responsible for providing operational support, coordinate projects and changes to the system. This role includes application support, system administration as well as ensuring GMP compliance of the system. You will closely interact with different departments (QC, logistic, QA, IT, OT)
Tasks and Responsibilities:
1st and 2nd Level Support/Troubleshooting for users of the LIMS Software application
Ensure that changes to the systems are appropriately implemented and communicated
Validation of new functions / applications, including creation of relevant documents such as functional specifications and test scripts
Drive further development and deployment of the new LIMS system
Support with LIMS-related DRs / CAPAs / CRs / INVs / EICRs
Monitoring and management of life cycle of SOPs
Support during external audits and inspections
Ensure the maintenance of local master data (e.g groups, components, units)
Your Profile:
Laboratory assistant / BSc or equivalent experience in life sciences and/or computer science (strong computer skills required)
Experience in the GMP regulated environment and in quality control
Several years of experience in dealing with pharmaceutical/laboratory software (Documentum, LIMS, SAP, TrackWise)
Experienced handling of common software applications (MS Office) and a strong interest in working with computer-based systems
Knowledge in computerized system validation (CSV) is an advantage
Fluent language skills in German and English (written and oral)
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