Preparation and review of QC documents as per cGMP requirement , Review of Raw material, finished product and Intermediate documents , Ensuring co-operation between all sections of QC department , Handling QC Deviations and CAPA related to QC deprt.
B.Sc. with 15 to 20 yrs / M.Sc. with 12 to 15 yrs experience. Should have handled audits such as USFDA, WHO-GMP, EDQM/COS, KFDA, etc. (Reporting to Sr. Manager)