LTIMindtree Canada seeks a QA/QMS skilled with strong knowledge of pharmaceutical QMS laboratory systems spanning the complete lifecycle. You will handle Veeva deviations and CAPA, raise ITCRs in ServiceNow with proper change descriptions, and perform root cause analyses and validation activities across laboratory systems.
The role requires experience with ValGenesis validation tools, extensive understanding of 21 CFR Part 11, GAMP 5 and other GxP standards, and crafting qualification
📌 Pharma QMS Consultant: Deviations, CAPA & Validation (Winnipeg)
🏢 LTM
📍 Winnipeg