Qureos Mentor

CORBETT INDUSTRIES

Audit Documentation:Role Purpose:To manage and control all quality-related documentation in the pharmaceutical manufacturing unit, ensuring full compliance with CDSCO (Central) and State Government regulations. The Senior Quality Analyst will keep the site audit-ready by maintaining accurate, complete, and compliant records.Key Responsibilities:<ul><li>Prepare and organize all documentation required for CDSCO and State FDA inspections.</li><li>Maintain audit-ready files, records, and logs at all times.</li><li>Ensure timely and accurate responses to audit document requests.</li><li>SOP &amp; Master Documents:</li><li>Draft, review, update, and control Standard Operating Procedures (SOPs).</li><li>Manage issuance and control of master documents (BMR, BPR, specifications, test methods).</li><li>Ensure Good Documentation Practices (GDP) across all departments.</li><li>Batch Records &amp; Logs:</li><li>Review batch manufacturing and packaging records for completeness and correctness.</li><li>Verify logbooks, forms, and data entries before final approval.</li></ul>Job Type: Full-timePay: From &#8377;70,000.00 per monthWork Location: In personSpeak with the employer +91 9990928598

Senior Quality Analyst

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CORBETT INDUSTRIES

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Senior Quality Analyst