IT Validation Specialist at Neopharm Labs

Bravad • blainville, qc • Posted July 08, 2026

About the Role

Join Neopharm Labs as an IT Validation Specialist, driving compliance in laboratory systems. Leverage your expertise in validation protocols and data integrity in a supportive environment.
The role involves validating GxP-impacting computerized systems, developing validation plans, and reviewing documentation for compliance. You will collaborate closely with IT, Quality Assurance, and lab teams, ensuring a rigorously maintained validated state throughout the system lifecycle. Your strong analytical skills and attention to detail are essential for identifying and remediating validation deviations affecting data integrity and compliance.
Key Responsibilities:
• Plan and execute validation for GxP systems
• Develop and author validation plans and protocols
• Review validation deliverables and documentation
• Identify and remediate validation deviations
• Prepare comprehensive validation summary reports
Requirements:
• 5+ years in pharmaceuticals or medical devic...