4-5

Supervision of Labelling & Packing activities, Visual inspection, QMS, Documentation Equipment Operation, Labelling Machine, Track& Trace system, Manual Visual inspection, Packing activities, Documentation

Scale-up & Exhibit Batches, Tech Transfer (IR/SR/ER), Documentation, Troubleshooting & AN DA Evaluation

In- Process line monitoring and GMP Compliance. Real- time batch record review and documentation control.

Perform and verify line clearance, BMR / BPR review, and documentation accuracy to ensure error-free batch processing.

Intas Accord is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world.

FOLLOW SOPS, GMP, AND ASEPTIC CONDITIONS. PERFORM EQUIPMENT CLEANING AND OPERATION UNDER SUPERVISION. ASSIST IN BATCH MANUFACTURING ACTIVITIES AS PER BMR.

OSD (Tablet & Liquid) & Hormone Manufacturing, Granulation/Compression/Coating, Primary & Secondary Packing, Liquid Filling, BMR/BPR Documentation, SOP/Validation/QMS, Troubleshooting, Inventory & cGMP Compliance.

Knowledge of HPLC / GC Empower software / UV, FTIR, Polarimetry, KFT, ATT, Balances, pH, Malvern PSD, PXRD instrument. Knowledge of GLP.

Experience in Instruments Calibration & Qualification, Working standards Qualification, Chemicals Procurement, CSVMP of QC instrument and LIMS & SAP Operation and related to pharmaceutical industry