TAPAN KUMAR SETHI

Biju Patnaik University of Technology

B.Tech · CSE

N/A – June 30, 2022

Persistent Systems

Lead Quality Engineer

June 1, 2022 – Present

India

Support Automation Engineering (Offshore-PSL)

June 28, 2026 – Present

Worked in Support Automation Engineering, focusing on designing, testing, and ensuring the quality of automated support systems. Contributed to improving system reliability, validating workflows, identifying defects, and collaborating with cross-functional teams to enhance service efficiency. Performed functional, regression, smoke, and production support testing, and participated in build validations, branch cuts, and deployments to ensure timely, high-quality releases. Analysed requirements to design test strategies and executed manual and automated test cases for functional, regression, and system testing. Developed automation scripts to improve efficiency and reduce manual effort. Performed smoke, production support, and deployment testing, including build verification and release activities. Identified and tracked defects, collaborating with development and DevOps teams for quick resolution. Ensured quality compliance through SDLC/STLC practices, reported test metrics, and contributed to continuous process and automation improvements.

Equity Trading & Risk Management Platform

June 28, 2026 – Present

Equity Trading and Risk Management Platform to provide a real-time trading system for equities, derivatives, and fixed income securities. The solution was designed to support front-office traders, middle-office risk managers, and back-office settlement teams. The platform handled trade execution, clearing, settlement, and risk monitoring with high performance and accuracy. It also integrated with global stock exchanges and clearing houses to ensure seamless trade lifecycle management. Key modules included: Trade Execution & Order Management System (OMS) – High-frequency trading with millisecond response. Risk & Compliance Module - Real-time monitoring of risk exposure, P&L, and regulatory compliance (MiFID II, Dodd-Frank). Settlement & Clearing - Automated settlement workflows with custodians and clearing houses. Reporting & Analytics - Trade reports, dashboards, and compliance reporting. Gathered business requirements from trading, risk, and compliance teams for OMS, risk, and settlement modules. Supported Order Management System (OMS) configuration for equities, derivatives, and fixed income trading. Assisted in implementing real-time risk monitoring (P&L, exposure, margin checks). Coordinated with middle and back-office teams for trade lifecycle automation (execution → clearing → settlement). Ensured compliance with MiFID II, Dodd-Frank, EMIR, and Basel III regulatory standards. Worked on integration with stock exchanges, clearing houses, and custodians using FIX and SWIFT protocols. Supported reporting & analytics by generating trade blotters, compliance reports, and dashboards. Participated in system testing (functional, UAT, regression) and defect tracking in JIRA/ALM. Conducted user training sessions for traders, risk managers, and settlement teams.

Veeva Vault – Quality and Regulatory Management System

June 28, 2026 – Present

Our client, a global pharmaceutical company, implemented Veeva Vault to manage regulated content and business processes across Quality, Regulatory, and Clinical domains. The goal of the project was to replace legacy systems with a cloud-based, GxP-compliant solution to handle SOPs, deviations, CAPAs, clinical trial documents, and regulatory submissions. The system was expected to ensure 21 CFR Part 11 compliance, maintain audit trails, enable electronic signatures, and provide role-based access control. The implementation included: Vault Quality Docs → To manage SOPs, CAPAs, Deviations, and Training. Vault RIM (Regulatory Information Management) → To manage global regulatory submissions and correspondence with Health Authorities. Vault Clinical Suite → To manage Trial Master File (TMF) documents, study protocols, and investigator brochures. Integrations → Integration with ERP (SAP), LIMS, and external regulatory portals for seamless data exchange. Gathered and analyzed business requirements for Quality Docs, RIM, and Clinical Suite modules. Participated in system configuration, validation, and testing activities to ensure GxP compliance. Supported end-to-end document lifecycle management including SOPs, CAPAs, Deviations, and Training records. Assisted in regulatory submission workflows (dossier tracking, correspondence with Health Authorities). Supported TMF management in Clinical Suite for inspection readiness. Coordinated with cross-functional teams for ERP (SAP), LIMS, and regulatory portal integrations. Conducted UAT sessions, user trainings, and created SOPs / work instructions for end-users. Generated compliance reports, audit logs, and dashboards for Quality and Regulatory metrics.