Responsibilities / Tasks
Roles & Responsibilities:
• 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 / Pharma jobs
• Execute the Stage Inspection / Final Inspection in order 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 evidences 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.
• Execute Vendor end Inspection to ensure timely completion of jobs.
Your Profile / Qualifications
Educational Background:
• Diploma/B E in Mechanical Engineering
Professional Knowledge and Experiences:
• ASNT NDT Level II in PT, RT, VT
• ISO 9001:2015 Internal Auditor from TUV Nord
• Aware with International Standards like ASME, ASTM, IS & GEA Niro Std & lean methodology.
Other Skills & Competencies:
• Microsoft Office Apps
• SAP
• Effective control over day to day activity
• Good Communication Skills
• Ownership
• Leadership qualities