Gaurav Mudadu
Thinker shaping strategies, Doer delivering results, Disruptor redefining industry through innovation
- Role
- Business Process Analyst at Tata Consultancy Services
- Location
- Mumbai, MH, IN
- LinkedIn followers
- 500 followers
About Gaurav Mudadu
Results-driven professional with experience in the Life Sciences domain at Tata…
Experience
Business Process Analyst
Feb 2025 — Present · Mumbai, IN
At TCS, the Human Biologics Management System (HBMS) process for GSK Life Sciences, supporting the end-to-end management of human biologics samples collected during global clinical trials. The HBMS process ensures accurate shipping, tracking, and lifecycle management of human biologics from clinical trial sites to central laboratories, adhering to stringent GxP compliance and regulatory requirements.Key Responsibilities & Contributions:Process Management: Oversaw the complete HBMS workflow, from sample initiation to study closeout, ensuring all activities met regulatory and sponsor timelines.Shipment Tracking: Coordinated and monitored real-time logistics and cold chain movements for biologic samples, resolving shipment delays and discrepancies promptly.Stakeholder Coordination: Acted as a liaison between clinical trial sites, central labs, courier partners, and GSK teams to ensure smooth operational flow.Data Accuracy & Compliance: Verified documentation, shipment manifests, and chain-of-custody records in compliance with ICH-GCP, GLP, and regulatory standards.Issue Resolution: Identified process gaps, conducted root cause analyses, and implemented corrective actions to improve operational efficiency.Reporting & Documentation: Maintained detailed status reports, trackers, and study-specific dashboards for internal and sponsor review.Process Improvement: Contributed to workflow optimization initiatives, reducing turnaround time for sample delivery and data reconciliation.This role strengthened my expertise in clinical supply chain management, life sciences operations, and cross-functional stakeholder management while deepening my understanding of global regulatory compliance in the pharmaceutical domain.
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