Senior Officer QA
- Location
- Pardi, Gujarat, India
- Work mode
- On-site
- Employment type
- Full-time
About the job
Experience: 1-3 years
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
From Meril Medical Innovations Privatelimited's careers page (Zoho Recruit), checked 29 Oct 2026.
How to apply
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Posted 14 Oct 2026 · checked 29 Oct 2026 · Report this job