Manager-QC

Piramal Pharma Limited

Location

Dhar | India

Job description

Plan the Analysis of stability samples as per cGMP requirement in time.
Analysis of Raw Materials / Finished Products / Stability Samples and related documentation as per cGMP requirement.
Ensure analysis of Raw Materials / Finished Products / Stability Samples as per requirement from outside commercial lab.
Calibration of instruments, as and when required.
Preparation and Standardization of Solution, as and when required.
Maintenance of Stability Incubators.
Loading & removal of samples from Incubators & documentation.
Entry of data in system.
Allocate works to workmen and trains them.

B.Pharma/ M.Sc

Job tags

Salary