Application Support Specialist

Experis Switzerland; Visp; Vor Ort; CHF 80’000 - 100’000; Vollzeit

Zusammenfassung

An established industry player in Visp is seeking a LIMS/SAP Systems Support Specialist to enhance quality unit support. This role involves operational support, system administration, and ensuring compliance with GMP standards. You will engage with various departments while providing troubleshooting assistance for LIMS software. Ideal candidates should possess a BSc in Life Sciences or Computer Science, have experience in GMP environments, and be fluent in both German and English. Join a forward-thinking team where your expertise will contribute significantly to the success of pharmaceutical operations.

Qualifikationen

• BSc in Life Sciences or Computer Science required with strong computer skills.
• Experience in GMP regulated environments and quality control is essential.

Aufgaben

• Provide 1st and 2nd Level Support for LIMS Software users.
• Drive development and deployment of the new LIMS system.

Kenntnisse

GMP Compliance

Troubleshooting

Computerized System Validation (CSV)

Fluent in German

Fluent in English

Ausbildung

Laboratory Assistant / BSc in Life Sciences or Computer Science

Tools

LIMS Software

SAP

Documentum

TrackWise

MS Office

Jobbeschreibung

Description:

The Visp site is looking for a LIMS/SAP Systems Support Specialist (f/m/d) (80 -100%) for the quality unit support team (QUS-LIMS-Visp). You will be responsible for providing operational support, coordinating 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:

1. 1st and 2nd Level Support/Troubleshooting for users of the LIMS Software application
2. Ensure that changes to the systems are appropriately implemented and communicated
3. Validation of new functions/applications, including creation of relevant documents such as functional specifications and test scripts
4. Drive further development and deployment of the new LIMS system
5. Support with LIMS-related DRs / CAPAs / CRs / INVs / EICRs
6. Monitoring and management of the life cycle of SOPs
7. Support during external audits and inspections
8. Ensure the maintenance of local master data (e.g. groups, components, units)

Key requirements:

1. Laboratory assistant / BSc or equivalent experience in life sciences and/or computer science (strong computer skills required)
2. Experience in the GMP regulated environment and in quality control
3. Several years of experience in dealing with pharmaceutical/laboratory software (Documentum, LIMS, SAP, TrackWise)
4. Experienced handling of common software applications (MS Office) and a strong interest in working with computer-based systems
5. Knowledge in computerized system validation (CSV) is an advantage
6. Fluent language skills in German and English (written and oral)