Analysis of Finished products / raw materials/ in process & stability samples
Day to day handling of hurdles for smooth analytical work
Reporting of deviations in analysis as per LIR procedure and implementation of CAPA.
Required Candidate profile
Knowledge of cGMP & GLP guidelines, ICH/ USFDA guidelines.
Handling of instruments like HPLC/GC/GCHS/Spectrophotometer etc.
Minimum 6 years of experience in Pharmaceutical industry and extensive