Application Support Specialist
Location: Visp
Sector: Other
Job Type: contract
Salary: Negotiable
Reference: BBBH608320
Description:
The Visp site is looking for a LIMS/SAP Systems Support Specialist (f/m/d) (80 -100%) for quality unit support team (QUS-LIMS- Visp). 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).
Key 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)
Key requirements:
* 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)
Key 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)
Key requirements:
* 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)
Contact: alba.jansa(at)experis.ch
