Job Description

Position: Officer

Department: Quality Control

Education Qualifications: B. Pharma 

Total Work Experience: 1-3 Years

Job Role: Finish Product section

Responsibilities:

Analysis of Finished Product samples /Process Validation samples /Stability samples/ RM. Samples /Cleaning validation samples and Beta-lactam containment monitoring samples as per SAP Request /Process Validation Protocol /Stability Protocol /and Cleaning validation protocol and STP’s. Documentation of analytical activity performed. Document analytical data and calculate results. To assist in investigation of OOS /OOT/Deviation /Lab Events. Management of Finished Product /Process Validation samples as per respective SOP’s. Ensure integrity, accuracy and adequacy of the analysis performed. Document data accurately and maintain neat/concise/organized Finished Product /Process Validation records. Ensure compliance to cGMP requirements and laboratory procedures. Preparation of RAPS (Record of analysis) of FP/PV Whenever required. To participate in analytical method transfer and analytical method Validation activity (Like analysis, Documentation & reporting of results).   Timely Place the indents & Procurements of Laboratory chemical & Consumables.  Recording of results in SAP system.