Production

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

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.

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.

Hetero is one of world’s leading producers of key Active Pharmaceutical Ingredients and generic formulations with presence in 140+ countries and backed by 30 years of experience in the pharma sector.

M.Sc. Chemistry, B.Sc. Chemistry, M. Pharmacy, B. Pharmacy, ITI Fitters, ITI Electrical, Diploma Safety, Diploma Mechanical

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

Experience in preparation of Sops. Handling of QMS elements viz. preparation of change control proposal, action items creation, shop floor investigation and preparation of investigation reports.