Job Requirements:
- Experience in Pharma domain
- Knowledge of GxP, 21 CFR Part 11
- Experience in Computer System Validation (CSV)
- Knowledge of IQ, OQ, PQ documentation
- Good communication skills
Key Responsibilities
- Review new system requirements.
● Prepare validation documents.
● Conduct risk assessments.
● Execute IQ/OQ/PQ protocols.
● Coordinate with IT, Quality Assurance (QA), Engineering, and vendors.
● Review deviations and change requests.
● Maintain validation records.
● Support audits and regulatory inspections.
● Ensure ongoing compliance with applicable regulatory requirements.
Pay: ₹25,000.00 - ₹27,000.00 per month
Work Location: In person
