Apply Now »

Title:  Senior Executive

Date:  Mar 10, 2025
Location:  Dewas SGO - Quality Control
Company:  Sun Pharmaceutical Industries Ltd

Job Description

Position: QC Engineer   

Department: Quality Control

Designation: Sr. Officer / Executive

Total Years of experience: 4+ Years

Education Qualification: BE in Electrical & Electronics

Job Role: QC Instrument Engineer

Responsibilities:

  • Preventive maintenance of all QC / IPQA (CQC/EB Lab/Block F/IPQA Block A,B,C,P/Sampling area A,B,C/PM Labs) of manufacturing.
  • Handling of all QC/IPQA Labs (CQC/EB Lab/Block F/IPQA Block A,B,C,P/Sampling area A,B,C/PM Labs) of manufacturing.
  • Performing lamp energy of all HPLC instrument.
  • Manage AMC/CMC contract with external vendor
  • Responsibility to maintaining instrument lsit/PM calendar /Quarantine list.
  • Support for review the document related to instrumentation (PPV, SPR and PTS, Qualification, Investigation, software validation / Software administration.
  • CQMS related activity for preventive maintenance and breakdown of instruments.
  • Manage spare inventory/PM kits for QC lab instruments.
  • Coordinate with procurement team (site person, account, purchase and vendor) for timely procurement of spare parts.
  • Follow ups for indent/PR/PO /Road permit/Shipment /GRN/RGP and NRGP or service clearance.
  • Activity based training provided to external vendor engineer, before start internal activity. Internal activity.
  • Handling /Implementation of corrective action and preventive action (CAPA).
  • Support provided for installation/qualification /calibration/shifting and retirement of QC instruments.
  • Coordinate with external vendor for preventive maintenance and breakdown and instruments related support activity like phase out/ upgradation activity.
  • Coordinate with internal plant engineering team for utility related activity.
  • Support provided for SOP preparation /Revision to internal team.
  • Extended support provided to micro lab for instruments.
  • Provided activity based training to QC user for optimum uses of all instruments.
  • Ensure compliance to cGxP requirements and safety standard in the laboratory procedure.
  • Ensure data integrity, accuracy, and adequacy of the documentation.
  • Document data accurately and maintain neat/concise /organized records.

Apply Now »