Manager QC

3 days ago


Surat, Gujarat, India Ciel HR Full time ₹ 5,00,000 - ₹ 10,00,000 per year
  • Follow the standard operating procedure (SOP) relevant to the analysis of the products.
  • Review of verification & method validation protocols for analytical methods inclusive of Assay, related substances and residual solvent.
  • Responsible to resolve any regulatory queries related to analytical methods and related impurities.
  • To receive the documents viz, Specification, SOP, Formats and test protocols etc. as required for the system.
  • Manage the compliance to each deficiency found in the quality control system.
  • Establishing specification and method of analysis of RM, PM, & FP.
  • Ensure completeness of documentation and validation of process & analytical methods as per cGMP requirements.
  • To maintain discipline at QC department.
  • Involved in the Analytical Method development and Validation Activities.
  • Resources and Man Power Management.
  • Authority to approve or disapprove any material viz., RM/PM/INT/FP or any incoming material subjected to quality matters, on consultation with Head Quality if require.
  • Report directly to the Head Quality on quality related matter.
  • In absence, Executive – QC or Officer – QC shall look after the work.
  • Review of In-process testing report, Raw material Testing Report, Packing material testing report and FP testing report.
  • Review of Calibration analytical instruments as per calibration planner. Record.
  • Monitoring of Laboratory chemicals.
  • Purchase requisition slip in SAP system Approved.
  • RM/PM/FP result Review and approve in SAP system.
  • New MIC Create in SAP System (new product create MIC in SAP system & any Pharmacopeia change create MIC).
  • Lab Chemical Received and Lab Chemical issue entry in SAP system.
  • Service PR approve in SAP system.
  • Revise SOP as and when required. Prepare new SOP as per requirement.

Ciel HR



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