16 Oct
|
Meril
|
Killa-pardi
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 (Killa-pardi)
🏢 Meril
📍 Killa-pardi