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.