Laboratory Information Management System

Overview

We are seeking a LIMS Specialist to join our GMP-regulated laboratory environment. The ideal candidate will manage day-to-day LIMS operations, lead and execute GMP validation and computerized system validation (CSV) activities, support system configuration and integration, and perform hands-on development where required. Strong French and English communication skills and adherence to regulated quality standards are essential.

Responsibilities

• Administer and maintain the Labware LIMS platform to ensure reliable, secure, and compliant operation in a GMP environment.
• Plan, execute and document GMP validation/CSV activities for LIMS changes, upgrades and integrations.
• Develop, review and maintain SOPs, work instructions and validation documentation related to LIMS operation and change control.
• Provide day-to-day operational support: access roles, troubleshooting, incident management and routine maintenance.
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