FEATURED JOB

Senior Executive

Cadila Pharmaceuticals Ltd

0 Years

Not disclosed

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Posted: 05 Sep 26

Job Description

Shop-Floor QA / GMP Compliance Perform routine QA oversight of API manufacturing and packaging operations. Ensure manufacturing activities are performed according to approved SOPs, BMR/BPR, specifications, and GMP requirements. Conduct line clearance and area/equipment verification before commencement of manufacturing activities. Monitor critical manufacturing activities and ensure compliance with approved process parameters. Verify equipment status, cleaning status, calibration status, and area conditions. Ensure proper identification and status labeling of raw materials, intermediates, solvents, finished products, and equipment. Raise and document GMP observations and ensure timely corrective actions. 2. Batch Documentation & Review Review Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), equipment logbooks, and associated GMP documents. Ensure entries are complete, accurate, traceable, and contemporaneous. Review manufacturing yields, reconciliation, process parameters, IPC results, and deviations. Ensure batch documentation is completed and reviewed within the defined timelines. Support batch disposition/release activities in coordination with QA management. 3. Deviation, Investigation & CAPA Initiate, review, and support investigation of deviations, incidents, OOS/OOT, process failures, and market complaints, as applicable. Participate in root-cause analysis using appropriate investigation tools. Prepare and monitor CAPA plans and verify effectiveness. Ensure investigations are scientifically sound, properly documented, and completed within timelines. 4. Change Control Review and assess change controls related to manufacturing processes, equipment, facilities, materials, analytical methods, documents, and utilities. Coordinate with Production, QC, Engineering, Regulatory Affairs, and other functions for impact assessment. Monitor implementation of approved changes and ensure required documentation is completed. 5. SOP & Quality System Prepare, review, and revise SOPs, specifications, formats, protocols, and other quality documents. Ensure implementation of the site Quality Management System. Support periodic review of SOPs and controlled documents. Ensure training is completed before implementation of new or revised procedures. 6. Audit & Inspection Readiness Support internal audits, customer audits, regulatory inspections, and GMP audits. Prepare documents and records required for audits and inspections. Track audit observations and support timely implementation and closure of commitments. Maintain the assigned areas in an inspection-ready condition. 7. Training & Compliance Provide GMP and quality-system training to Production, QC, Warehouse, Engineering, and other relevant personnel. Monitor compliance with data integrity and good documentation practices. Promote a strong quality culture throughout the manufacturing area. 8. Cross-Functional Coordination Coordinate with Production, QC, Warehouse, Engineering, EHS, and Regulatory Affairs to resolve quality-related issues. Provide QA guidance during manufacturing process deviations and abnormal events. Support continuous improvement and risk-reduction initiatives. Required Knowledge Strong knowledge of ICH Q7, GMP, GDP, data integrity, and API manufacturing requirements. Knowledge of BMR/BPR review and shop-floor QA activities. Good understanding of deviations, CAPA, change control, OOS/OOT, investigations, and risk assessment. Familiarity with regulatory expectations for API manufacturing. Understanding of documentation practices and traceability requirements. Key Skills GMP and regulatory compliance Batch record review Deviation investigation CAPA and change control Root-cause analysis Audit/inspection handling Documentation and data integrity Problem-solving and decision-making Cross-functional coordination Team leadership and communication Key Performance Indicators (KPIs) Timely and accurate batch record review GMP compliance and reduction in recurring observations Timely closure of deviations, CAPA, and change controls Audit/inspection readiness and compliance Effectiveness of investigations and CAPA Training compliance Data integrity and documentation compliance Reduction in repeat deviations and quality incidents