Elevate your career as an IT Validation Specialist with Neopharm Labs. This role focuses on validating laboratory systems while ensuring compliance with industry standards and regulations. With over 30 years in the life sciences sector, Neopharm Labs is looking for a detail-oriented IT Validation Specialist.

This position requires expertise in Computer System Validation (CSV) and GxP systems to create and implement effective validation protocols. You'll work closely with IT, Quality Assurance, and laboratory teams to maintain compliance throughout system lifecycles. Key Responsibilities:
Execute validation of GxP-impacting computerized systems
Develop validation plans and protocols (VMP, VP, IQ/OQ/PQ)




Review and approve validation deliverables and reports
Document validation deviations and implement CAPAs
Prepare summary reports with results and recommendations Requirements:
Over 5 years in the pharmaceutical or medical device industry
Minimum 3 years in Computer System Validation (CSV)
Solid knowledge of ISPE GAMP 5 and FDA regulations
University degree in a relevant field
Bilingual in English and French Contribute your expertise in validation processes and compliance to enhance Neopharm Labs' commitment to health and innovation.

📌 It Validation Specialist At Neopharm Labs Blainville
🏢 GEXEL Télécom International
📍 Blainville