Officer

• To maintain and adherence of the GLP and safety procedures in laboratory. • To issuance of work data sheet / protocols from Q.A Department. • To work as Analyst and maintain the CFR 21 part -11 compliance by following laid down procedures. • To perform wet analysis of finished product/ returned goods / raw materials/ Hold time / Stability study / working standard analysis,(Test like Sulphated Ash/Residue on ignition/Specific Gravity/Water content by KF/Assay by manual or potentiometer titration, LOD/ Different type of limit test/ Melting / boiling point/ particle size analysis by air jet sieve/ particle size analysis by Malvern Mastersizer 3000/UV spectrophotometer / BD/TD, Polarimeter / IR Spectroscopy/spectrofluorophotometer/pH measurement etc) as per work allocation and records the results in work sheet (Protocol) as per current specification and method of analysis and maintain the on line documentation. • To Perform sampling of intermediates /returned goods / Hold time of intermediate sample / Stability study / Working standard samples and finished products as per laid down procedure. • If required report the analysis data in LIMS modules and report to Section – Head. • To ensure that every specification and method of analysis used of right product/material code. • To follow the instruction of Shift /Section In charge for analysis /planning. • To maintain instrument history record. • To report and raise any QI/NQI/OOS/OOT / Deviation/ discrepancy in laboratory analysis to QC- In charge.

Cadila Pharmaceuticals