5+

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.

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.)

Shopfloor IPQA & Real-time Process Monitoring, Process & Cleaning Validation (Protocols & Execution). APQR Preparation & CPV (Continued Process Verification)

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

Manage product registrations, renewals, and variations for international regions outside major regulated markets. Coordinate with local agents/distributors for regulatory submissions.