This opportunity is with India's leading IT Technology and consulting MNC for Hybrid work mode (PAN India Locations).

Role Overview

We are looking for experienced professionals with expertise in Computerized System Validation (CSV), Risk Management, Quality and Regulatory Compliance within the Pharmaceutical / Life Sciences industry.

The ideal candidate should have a solid understanding of pharmaceutical regulations, hands-on experience in validation activities, risk assessments, audits and quality management processes.

Key Responsibilities & Requirements

- Experience in the Life Sciences / Pharmaceutical industry, ith consulting services or industry exposure.
- Strong understanding of pharmaceutical compliance regulations, including 21 CFR Part 11, GxP and GAMP 5.
- Experience in creating, reviewing and approving / acknowledging CSV validation deliverables.
- Knowledge of risk management processes and quality management requirements for IT projects.
- Experience in validation of enterprise applications such as SAP / S4 HANA, TrackWise, QMS, DMS, etc.

📌 Consultant - CSV - Life Sciences (PAN India Location) (Bengaluru)
🏢 Edge Executive Search
📍 Bengaluru