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.
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
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