-Operate laboratory equipment and Prepare Daily sample solution for heavy metal analysis by following methods such as EN, ISO, ASTM, SNI, CPSC, and SGS Inhouse method-Know and have attended ISO 17025:2017 training-Qualitative and quanitative sample analysis using AAS, ICP OES, ICP MS and FTIR-Interpreting data output from instruments, Reporting analysis results, and review results before final checking by superior-Using LIMS to input final results-Responsible on daily, weekly and monthly maintenance of ICP MS to maintain performance and quality output of ICP MS analysis based on CILR-Able to do routine maintenance and performance check of ICP OES and AAS-Responsible in inventory control of consumables and sparepart of ICP MS, ICP OES, and AAS-Perform Proficiency tests for Extrachtable Heavy Metals in textile analysis from RRT, IIS, Waste Water from FAPAS, and Correlation test from NIKE-Ensuring HSE issues are in accordance with guidelines-Ensure full compliance with the SGS code of integrity & professional conduct and it all times adopt behavior in accordance with nondisclosure agreement and SGS codes of conduct-Actively involved in WCS (World Class Services) as AM/PM Pillar member, and QC (Quality Control) Pillar member-Already implementing some Kiazens and improvements in ICP-AA area-Familiar with 5W+1H, 5G, EWO, CILR, OEE, AM/PM Calendar, QA Matrix, OPL, PokaYoke, Error Proof, Visual management, Tags, Radar Chart, TWTTP, HERCA and etc

-Coordinate with chemist and internal teams, carry out costumer request on testing product-Research alternate raw materials and develop new formulas for water based and solvent based paintproducts.-Conduct evaluation on new raw materials, make comparison with current, analyze and report testingresults to superior

• Coordinate with superior and internal teams, carry out analysis chemical and phisical of medicine.• conduct routine analytical testing of semi finished good product accordance with ISO, PQS, CPOB,HALAL ptocedures, and Occupational Health and Safety (OHS) and the Environtment.• Operate Instruments for routine analysis, HPLC, Spectrophotometer UV-VIS, Dissolution tester, pHMeter, Disintegration Tester, and Hardness tester.• Review and evaluate the quality of HPLC, Spectrophotometer UV-VIS data analysis are in conformancewith QA/QC procedure.• Report and review the final result to superior and QA team• Working on kaizen with tools such as 5W+1H, 5G, Visual management, Tags, and etc.• Familiar with kanban, and Continous Improvements.

• Conduct routine analysis and microbiology testing of finished good product accordance with IFF QualityControl Testing Manual (QCTM).• Using instruments for routine analysis such as GC, GC-MS, Refractometer and Density meter, KarlFischer, and Potentiometric Titrator.• Conduct microbiology testing such as, Total Plate Count, Yeast and mold, Coliform (Most ProbableNumber), and Pathogenic Bacteria Testing.