Officer QC SGO

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Position:

Department:

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Job Role:

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.
  

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