including 5 yrs supporting Enterprise Quality System including ComplianceWire LMS, Veeva Document Management System, TrackWiseTrackWise Digital platform; 3 yrs managing validation documentation in paperless validation system such as ValGenesis and Regulatory publishinglabel management system; and 6 yrs as technical team lead exp can be gained concurrently; knowledge of GxP requirements and FDA regulatory requirements related to manufacture of pharmaceutical products.

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