Posted:8 hours ago|
Platform:
Work from Office
Full Time
Trackwise Strong understanding of CAPA Investigation workflows
LIMS Expertise in Labware modules Product LOT EM Stability Inventory etc ELN Method Execution LIMSBasic coding Crystal Reports
Documentum D2 Experience in document lifecycle management and regulatory compliance
Testing Tools HP ALM UFT Tosca Selenium Playwright
Technical SQL PLSQL SNOW customization debugging report generation
Compliance Familiarity with 21 CFR Part 11 GxP and pharma validation standards
Responsibility-
Lead endtoend functional and testing activities for Trackwise CAPA Investigation Labware LIMS v6v8 and Documentum D2
Manage stakeholder expectations and coordinate with crossfunctional teams including vendors and IT engineers
Oversee test strategy planning execution and defect management using tools like HP ALM and SNOW
Ensure compliance with pharma domain SOPs WI and validation protocols
Provide L3 support and troubleshoot performance issues across lab systems
Mentor and manage a team of 1215 members balancing technical 75 and managerial 25 responsibilities 1
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