Lims Administrator
View: 140
Update day: 16-11-2025
Location: Braine-l’Alleud Walloon Brabant
Category: Other
Industry:
Job type: Contract
Job content
At least 3-5 years’ experience in the Pharmaceutical industry or a similar operating environment, with a strong emphasis on QC systems, in particular LIMS.
Demonstrated ability to drive the completion of tasks.
Hands on experience with labware LIMS, ELN, Empower (NuGenesis, SDC & Optimu desired)
Working within a lab on a custom localized LIMS system
Understands the process for deploying sample plan and test plan
Hands on experience on any SAP-LIMS interface
Hands on experience in using any Oracle tools for IT related troubleshooting
Provided first level of IT response for password resets and local lab sample related activities
Experience in IT related documentation process (IQ/OQ & SDLC)
Experience in usage of any incident / problem and change management tools
Experience working in a GMP laboratory facility
Should possess Incident/Request/Problem and change controls following ITIL principles.
Good written and verbal communication skills to effectively communicate with technical and business users.
Knowledge in GxP terms as per 21 CFR PART 11, Compliance issues and Documentation.
Ensure that LIMS, ELN, Empower is maintained and streamlined were possible.
Coordinate and communicate the prioritisation of updates and changes in LIMS, ELN, Empower to all impacted users.
Complete training as required with LIMS, ELN, Empower users.
Support the review & approval of key quality deliverables including LIMS, Change control, trackwise, Deviations, CAPAs. Etc.
Review & approval of GMP procedures (& associated documents) for the lab
Coordinate and support with respective groups/departments and product vendor for system administration or any patching maintenance or hypercare activities after patch or system upgrades
Attend periodic review meetings, cutover migration, hypercare support, any enhancements planning, design and/or implementation meetings as required.
Good at customer handling and liaising with all stakeholders.
Deadline: 31-12-2025
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