Cadila Pharmaceuticals

- To prepare, review and submit dossiers for Life cycle management, and other submissions as required for EU region. - Preparation, review and submission of eCTD Renewal, variations, post marketing a

Key Responsibilities A. Analytical Method Development & Optimization Develop, optimize, and establish analytical methods for pharmaceutical formulations and development samples. Perform analyti

Execute manufacturing activities for API intermediates and finished active pharmaceutical ingredients as per approved Batch Manufacturing Records (BMRs), SOPs, and production plans. Operate and monit

Execute batch manufacturing activities as per Batch Manufacturing Record (BMR), SOPs, and approved process parameters. Operate and monitor reactors, centrifuges, ANFD, dryers, filters, and associated

Execute manufacturing activities for API intermediates and finished active pharmaceutical ingredients as per approved Batch Manufacturing Records (BMRs), SOPs, and production plans. Operate and monit

Review and approve batch manufacturing records (BMR), batch packaging records (BPR), logbooks, and analytical reports. Perform line clearance activities before and after manufacturing operations. Mo

Execute manufacturing activities for API intermediates and finished active pharmaceutical ingredients as per approved Batch Manufacturing Records (BMRs), SOPs, and production plans. Operate and monit

Execute manufacturing operations as per approved Batch Manufacturing Records (BMR), SOPs, and production plans. Supervise shift activities and ensure timely completion of production batches. Handle

Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process condi

Execute API manufacturing activities as per Batch Manufacturing Records (BMR) and SOPs. Monitor and control unit operations such as charging, reaction, filtration, centrifugation, drying, milling, bl