SENIOR EXECUTIVE/EXECUTIVE QUALITY MANAGEMENT

1. To uphold company's policy on quality throughout the organization, at all times. 2. Responsible for maintaining compliance with ISO 13485: Medical Devices - Quality Management system - Requirements for Regulatory purposes, MS2636: Halal Medical Devices - General requirements and related current Good Manufacturing Practices - cGMP (e.g. Pharmaceutical Inspection Convention/Scheme standards. 3. Responsible for establishment & review of documentation related to Quality system (e.g. Standard Operating Procedure, Batch Manufacturing Records, Worksheets). 4. Responsible for management of calibration activities. 5. Responsible for all activities under Quality Management Department.