Salary not disclosed
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Role overview
Job description
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
About this listing
- Source: Meril Life Sciences's official careers site · still listed there on 9 Nov 2026
- Posted 14 Oct 2026
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What they are looking for
Skills & requirements
Qualification
Job Responsibility - Monitoring of qualification and validation activities; Preparation and review of qualification & validation protocols and reports
Hiring company
Meril Life Sciences
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₹20L – ₹30L/yr
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