We are seeking a LIMS Validation Specialist to support the configuration, validation, and optimization of our Laboratory Information Management System. This role bridges IT and Quality Control, ensuring that laboratory processes are accurately reflected in the system and compliant with GMP standards. If you have solid experience in QC, LIMS, and CSV, and you're looking for a flexible hybrid opportunity-this role is for you.

Mission Description

We are looking for a Validation Specialist to support and manage our LIMS (Laboratory Information Management System) activities. Your responsibilities will include:

• Creating templates and master data within the LIMS system.
• Understanding and managing test methods, specifications, and related master data.
• Ensuring compliance with GMP documentation standards.
• Supporting CSV (Computer System Validation) deployment and activities.
• Collaborating closely with Quality Control (QC) teams to ensure the system configuration aligns with laboratory workflows.
• Working with IT teams on system architecture and integration efforts.

Profile Requirements

• Minimum 5 years of experience in a similar role.
• Practical experience with QC processes and LIMS systems.
• Strong knowledge of GMP regulations and documentation best practices.
• Prior involvement in CSV activities.
• Fluent in English or Frensh.