Responsibilities / Tasks
- To be familiar with, and act in accordance with, all relevant health & safety management, legislation and company quality system rules, regulations, and policies.
- Follow the Company's Quality Management System / Procedures / Processes in line with ISO 9001:2015 Quality Standards.
- To maintain a formalized set of procedures, work instructions / Procedures / SOPs and standards to support the Company's Quality Management System.
- Responsible for Quality Control of Product Range Non-Pharma and Pharma jobs.
- Execute the Stage Inspection / Final Inspection to ensure timely completion of jobs.
- Execute Vendor end Inspection to ensure timely completion of jobs.
- Ensure effective utilization of ITPs during stage and conduct PDI after final Inspection of the job.
- Ensure NDT (VT, RT and DPT) are successfully carried out and the evidence are in the backup folder for fast document processing.
- To attend the "Customer Inspection" and FAT of Non-Pharma / Pharma Projects.
- To ensure that full traceability of all materials and components is maintained and fully documented throughout all areas of activity, including all stainless steels, bought-out-items, and sub-assemblies
- To manage stage Inspections and Lot clearance in SAP.
- Responsible for Calibration and safekeeping of measuring instruments.
- Actively Participate in 5S / Kaizen and Lean Six Sigma Projects.
Your Profile / Qualifications
Educational Background
- Diploma/B E in Mechanical Engineering.
- ASNT NDT Level II in PT, RT, VT.
- ISO 9001:2015 Internal Auditor.
- Aware with International Standards like ASME, ASTM, IS & GEA Niro Std & lean methodology.
- PED Certified Equipment knowledge.
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