RecruiterPK

Description

Respected Sir,
I have almost 10years of Pharma experience in QA and have sound knowledge about sterile and non sterile area.Audit of BMR (Batch manufacturing record).
Release of finished goods.
Maintain data record.
Co-ordination of APR (Annual product review).
Revision of BMR.
Revision of SOP’s.
Microbial swab testing.
Particle count in Sterile Area.
Inspection of air flow.
Inspection of manufacturing area (Liquid or Solid).
Inspection of Packaging area.
Inspection of Encapsulation.
Internal calibration of equipment’s used during IPC.
Documentation record.
Collection of Reference samples.
Dispensing of active and excipients.
Analysis of Packaging material.
Sampling of Raw Materials for analysis.
Organize Training Seminars.
Area Inspection or Line clearance (In process control).
Deviation and its record.
Maintenance of data for drug Stability.
Running of ERP on finger tips.
Co-ordination of batch for Validation.
Issuance of BMR and Batch #.
Reconciliation of MO or PO used in BMR.

Regards,
Dr.M.Umer Hafeez
03172263273

03018264404

03343556238