2-3

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

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

Providing input into final analyses and interpretation including the development of the Clinical Study Reports, publications, and internal / external presentations.

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.

ITI / Diploma for Operators (Sterile USFDA Exp.) B.Pharm / M.Pharm for Officer (Sterile USFDA Exp.)

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