||1.Good knowledge on GC & HPLC
2.Ensure that process and quality guideline are adhered to by Following QC and QA SOPs, Pharmacopeias,cGMP, cGLP and safety precautions at the work area .Continually evaluates systems for improvement opportunities.
3.Need to handle team of 10 members
4.Audit compliance, proper investigation of incidents, deviations, OOS (Out of Specification results), OOT (Out of Trend results) and CAPA
5.Ensure analysis using instrumentation by the team.Complete review of intermediate, finished products through instrumentation
6.Ensure updation of analytical data, log books and other documentation
online. Maintain records and data integrity.
7.To manage Analytical Method Validation and Quality Management System ( QMS)
8.To Prepare and review of method validation protocol / report , SOP &, Test procedures.
9.To Manage Analytical method transfer activities