Senior Officer QA

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