LTI
Senior Consultant - System Management
This job is now closed
Job Description
- Req#: 1249864
Location: Bengaluru-LTR Campus Whitefield
Exp: 3-5 Yrs
SPOC: Jaskaran.singh3@LTIMindtree.com
Key Skills: Trackwise/Tracelink
Job Description: "* Experience in Trackwise is a must and work experience on TrackWise Team Access & Web Admin , Crystal Reports, Web admin components, Utilize TrackWise import utilities proficiently and TrackWise Coordinator (Admin Query, Dynamic Query, Program Sequence)
Providing resolution of critical TrackWise issues. (Ex- Workflow is not working as expected, User/Group is not receiving notifications, Application is not working, Crystal Report issues, Advising users whenever they have knowledge gap, Webservices not behaving expectedly, Report Template is slowing down the system, Dashboard query is causing performance issue, Ad-hoc database report, Users not able to interact with a record and so on.)
* Monitoring activities are part of these requirements, like (DB Health, Coordinator stuck, RAS, Null pointer, PR Stuck due to Web Service, Individual Server URL health, Product Lookup, Disk space alert)
* Should have indepth knowledge of handling Quality management in TrackWise
Should have a strong understanding of Trackwise Business processes such as Change Management System, Incident/Deviation Investigation, CAPA implementation etc.
Should have a deep understanding of the individual workflows/approvals in each Trackwise Module.
* Experienced in generating various types of queries in TrackWise requirements.
Well versed knowledge of Quality Risk assessment through TrackWise Application
Should have managed QMS implementation projects including configuration migrations, data migration, multi-site rollouts, data archival etc.
* Should have adequate knowledge in performing gap assessments from an end user perspective.
* Need to ensure quality assurance procedures are followed and in accordance with Customer’s methodology and standards.
* Minimum 2 years of experience in a Pharmaceutical/Life Sciences setting is preferred.
* Experience with industry-standard and best practices regarding quality, quality assurance and quality control principles and techniques (e.g., 21 CFR Part 11, GAMP 5)
* Versed in health authority regulations such as FDA, 21 CFR, MHRA Annex 11
Subject Matter Expert in GxP (GDP, GLP, GMP) and Data Integrity."
About the company
Larsen & Toubro Infotech Limited is an Indian global Information technology solutions and services company based in Mumbai, India.
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