Review of analytical reports Raw material,
Packing material, In process, Stability study,
analytical method validation protocols/ reports,
Calibration, instrument qualification,
Working standard qualification, analyst qualification etc.
for compliance of the data as per statutory
Verifications of Certificate of analysis
Responsible for Review of QMS Documents (e.g. OOS, OOT, Incident, Deviation and Change control).
Responsible for review of electronic data to ensure the data Attributable, Legible,Contemporaneous,Original & Accurate.
Responsible to handle regulatory inspections
Review of SOP’s related to Quality Control.
Required Candidate profile
Analytical QA with min 2-7 yrs of experience in Pharma