QC

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.

Handling and Reviewing of the documents related to Instrument i.e HPLC- Dissolution.

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

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.

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