Pharma QMS Consultant: Deviations, CAPA & Validation
LTIMindtree Canada seeks a QA/QMS professional with strong 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 GxP standards, and crafting qualification
We are currently recruiting a Pharma QMS Consultant:
Deviations, CAPA & Validation for our team in Canada.
The position is based in Canada.
This opportunity is part of our work in IT & Technology.
The advertised compensation is 110..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).