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Title:  Executive - Analytical Development

Date:  May 22, 2025
Location:  Tandalja - R&D
Company:  Sun Pharmaceutical Industries Ltd
  • To work as per cGMP and ensure its compliance as per current guideline and SOPs.
  • Responsible to take training before execution of allotted work & maintaining the training file.
  • Responsible to follow safety precaution as per laboratory procedure.
  • Responsible to escalate any issue / incident to reporting manager for prompt corrective action.
  • Responsible for method development studies for various finished products.
  • Responsible for method Validation studies for various finished products.
  • Responsible for routine and stability studies of various finished products.
  • Responsible to align with organization goal.
  • Other responsibilities assigned by reporting authority. 
  • Responsible to follow Quality Management Document procedure. 
  • Responsible to perform the calibration of instrument.
  • Responsible to prepare Study Protocol and Study Reports.
  • Responsible to maintain instrument/equipment as per SOPs.
  • Responsible for timely archival of documents as per SOP.
  • Responsible to follow safety precaution as per laboratory procedure.
  • Responsible to ensure proper Handling and Disposal of waste.

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