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Title:  Sr. Officer - NPQC

Date:  Mar 25, 2025
Location:  Mohali - Plant
Company:  Sun Pharmaceutical Industries Ltd

RESPONSIBILITY :

  1. Analyze Finished Product/process validation samples/Stability/Swab sample and Raw Materials allotted for testing using HPLC, GC, Dissolution Rate apparatus, FTIR, UV, KF, and DT Apparatus etc. Tablet hardness tester, Friability apparatus and Loss on Drying (LOD), etc. as per Stability protocol and Test procedure.
  2. Recording and calculation of analytical data.
  3. Destruction of left over samples and expired Raw materials.
  4. Enter analytical data in SAP and generate COA (Certificate of analysis data).
  5. To follow compliance to cGMP requirements and laboratory procedures for integrity, accuracy and adequacy of the analysis performed.
  6. Analysis and reporting as per work allotment and hand over analytical reports to lab in-charge/reviewer at the end of the shift.
  7. To follow E.H.S (Environment, health and safety) policies.
  8. Timely inform the lab in charge or manager about any Lab event, OOS/OOT and deviation.

 

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