Cadila Pharmaceuticals

Ensure accurate and timely completion of: Batch Manufacturing Records (BMR) Equipment Logbooks Cleaning Records Calibration Records Usage Logs Shift Reports Maintain compliance with cGMP, GDP,

Execute batch manufacturing activities as per approved Batch Manufacturing Record (BMR). Supervise batch charging, reaction monitoring, filtration, centrifugation, drying, milling, blending, and pack

Ensure in-process controls are performed as per specifications. Coordinate with QA/QC for sampling, analysis, line clearance, and batch release. Raise and investigate deviations, OOS, OOT, CAPA, and

Ensure accurate and timely completion of: Batch Manufacturing Records (BMR) Equipment Logbooks Cleaning Records Calibration Records Usage Logs Shift Reports Maintain compliance with cGMP, GDP,

• Ensure the development progress periodically of personals and take necessary corrective action. • To lead the Granulation department with respect to developing the second line. • To ensure the del

Ensure accurate and timely completion of: Batch Manufacturing Records (BMR) Equipment Logbooks Cleaning Records Calibration Records Usage Logs Shift Reports Maintain compliance with cGMP, GDP,

Responsible rDNA manufacturing and parenteral mfg activities at Dholka premises. • To do aseptic area entry exit procedure properly with proper gowning. • To check and ensure that differential press

Prepare, review, and maintain Batch Manufacturing Records (BMRs) and Batch Packing Records (BPRs), where applicable. Ensure real-time and accurate recording of manufacturing activities in compliance

Documentation: • To prepare SOP’s/ URS/ BPR/ Protocol/ Investigation report for regulatory compliance as per available procedure/practice. • Ensure that all documents / records required for Regulato

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