Job description
B.Pharm / M.Pharm with 5 to 7 years of experience in QC Department. Analysis of raw material, finish product, in-process samples, validation sample & stability samples by instruments like HPLC. Review of calibration activity of all instruments.
Required Candidate profile
Responsible for the analysis of validation samples & maintenance of related documentation. Responsible for maintenance of working standards & reference standards. Responsible for calibration of HPLC. |