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Active3w ago

Senior Officer QA

Meril Life Sciences·📍 Pardi, Gujarat, India

Employment

FULL TIME

Work mode

On-site

Experience

1–3 years

Salary

Not disclosed

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

Healthcare

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