0-2 year experience in Medical Device/Pharma industry.
Job Responsibility
- Monitoring of qualification and validation activities.
- Preparation of technical files and related documentation.
- Preparation and review of qualification & validation protocols and reports.
- Review of raw data, including analytical reports, BMRs, job cards, batch release certificates, data mapping reports, etc.
- Support validation activities across multiple manufacturing segments
Requirements
Qualification & Validation (IQ/OQ/PQ)
Technical Documentation & Technical File Preparation
Protocol and Report Preparation & Review
Data Review & Documentation Verification
GMP Compliance & Regulatory Documentation
Batch Manufacturing Records (BMR) & Analytical Report Review
Cross-functional Coordination & Validation Support
📌 Senior Officer QA (India)
🏢 Meril
📍 India