Job Description
Knowledge of HPLC/GC / other instruments of QC.
Expertise of pharmaceutical quality system.
Analytical data review of formulation, API, and stability.
RM/FP/SS, OOS and OOT handling and report writing.
Working as QC analyst.
Understanding of current GMP requirement and regulatory requirement.
Understanding of laboratory instrument software validation and 21 CFR.
Work Experience
4 to 8 years