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: Prepare and organize all documentation required for CDSCO and State FDA inspections. Maintain audit-ready files, records, and logs at all times. Ensure timely and accurate responses to audit document requests. SOP & Master Documents: Draft, review, update, and control Standard Operating Procedures (SOPs). Manage issuance and control of master documents (BMR, BPR, specifications, test methods). Ensure Good Documentation Practices (GDP) across all departments. Batch Records & Logs: Review batch manufacturing and packaging records for completeness and correctness. Verify logbooks, forms, and data entries before final approval. Job Type: Full-time Pay: From ₹70,000.00 per month Work Location: In person Speak with the employer +91 9990928598