SCOPE / DIMENSIONS OF ROLE -To implement QMS ( Global manual / standard , ISO 9001 ) -Manufacturing QA ( Micro B and Hygienic management , 3rd Party QA -To Quality assurance of Intercompany products (Pharm, Quasi drug, Medical devices, Cosmetics, Supplements and Hygienic products, etc,) -To ensure 3rd Party Mgmt (RB intercompany and local Comakers) and Quality improvement -Supervise QC test (Importing FGs ) -MicroB and Hygienic management (eg. GMP, HACCP, etc,) -Quality tools application ( 6 Sigma, SPC/SQC, FMEA) and CI -Cowork for R&D, Marketing, Package for NPD/EPD project -Risk management and CAPA leading( Quality investigation and Complaint handling -Presentation and communication w/internal stakeholders( region and local ) RESPONSIBILITIES / ACCOUNTABILITIES -RB Global Quality standards(Manual, SOPs) implementation and Improvement -Ensures Quality improvement ( Quality investigation, FMEA, SPC/SQC application, etc,.) -Lead QC related issues and CAPAs -Maintain robust and effective change control system -Training for MicorB / Hygienic factory / Key Quality projects -To supervise QC lab. and QC data (MicroB, Regulated FGs) -RB QA audits (CAPA, F/U Monitoring) -To prepare products technical dossiers and quality standard document  BUSINESS MANAGEMENT SYSTEM -Responsible to develop and implement the global & local Business -Management System (BMS) to ensure fully compliant regulated products. -Work with local functions to develop and maintain all relevant procedures -Develop and maintain robust and effective change control system to ensure compliant Market Authorisations -Product Recall – establish and communicate responsibilities. Conduct mock recalls -Train all staff in commercial organisation on all activities required by BMS -Responsible for initial assessment and approval of Distributors & Embellishers handling regulated products -Prepare Technical Agreements for Distributors & Embellishers – define all expectations (change management, product handling, product release, responsibilities)