LTIMindtree Canada seeks a QA/QMS professional with robust knowledge of pharmaceutical QMS laboratory systems spanning the complete lifecycle. You will handle Veeva deviations and CAPA, raise ITCRs in Service Now with proper change descriptions, and perform root cause analyses and validation activities across laboratory systems.The role requires experience with Val Genesis validation tools, extensive understanding of 21 CFR Part 11, GAMP 5 and other Gx P standards, and crafting qualification#J-18808-Ljbffr