Ensuring process validation and calibration of analytical apparatus Ensuring training, including the application and principles of quality assurance Ensuring designation and monitoring of storage conditions for materials and products Ensuring performance and evaluation of in-process controls To ensure good
#Candidate should have exposure of in-process/process validation/analytical data review/stability #Experience of instruments like HPLC, UV-Spectrophotometer, Particle Size Analyser, KF-Autotitrator (Metrohm), Dissolution test apparatus, ICPMS. #Knowledge of quality management system #Should handle USFDA & MHRA Audit #Should have exposure in API Plant #Qualification: B.Pharma/ M.Pharma/ B.Sc/ M.Sc #Pleasant Personality ...
Producing API and intermediate of desired quality Batch output and its economics, targeted productions, cGMP & HSE audit reports Compliance of Pharmaceuticals / group requirements, targeted reduction in consumption of recovered solvents. Adherence and compliance to cGMP & CHSE norms achieving
To assist the Management in executing all GMP / GLP related activities To monitor and prepare budgetary provisions To co-ordinate with Head of manufacturing, Stores, Production and maintenance Handling of Market Complaints, Returns /Recall, Deviations, OOS, Validation report review. Vendor on site