Trần Thị Huyền Trân

Knowledge of laboratory instruments, preservation. ➢ Experience with Microsoft Office Applications including Word, Excel, PowerPoint, and Outlook. ➢ In-depth knowledge in CGMP, ISO 9001, TS16949 regulations/guidelines. ➢ Regulate, managing the time a reasonably. ➢ To have a sense of responsibility ➢ Ability to communicate in English ➢ I can work in groups or independent

EXPERIENCE 2010: Working at Quatest 3, Bien Hoa City; Position: staff analysis Analysis of the target in the samples by the customer brought to • .Analysis of the chemical targets in the cement standar TCVN 141 -2008 (Analysis a number of targets MgO, CaO, Fe2O3, Al2O3, SO3…in the cement) • Analysis of the chemical targets in the cement standar and ASTM C114 – 2003 (Analysis a number of targets MgO, CaO, Fe2O3, Al2O3, SO3, R2O3, TiO2, P2O5…in the cement). • Measurement of surface tension of some kind lubringcating oil. 2010 – 2011: New Choice Food , Binh Duong City Position: QA lab technician Microbiological testing. • Microbiological testing of material, finished product and semifinished product (such as targets: total plate count, coliform, ecoli, yeast and mold, salmonella, staphylococcus aureus…). • Testing the micro air in production areas. • Testing conditions of sanitation workers. • Checking the input raw-materials (such as : agar, koniao, sugar, acid citrit, acid malic, food coloring, flavouring….) • Report the job every day, every week, every month on the Excel, MS. Word, Powerpoint. • Calibrate equipments and instruments . • Setting up the form evrymonth. • Strorage and preservation of samples of finished products. 2011 – 2015: Logoplaste Viet Nam, Binh Duong City Position: QA Supervisor • Supervises all quality assurance functions to achieve accurate and objective inspection in accordance with Company requirements. • Coordinates production schedules to ensure inspection programs are carried out effectively. • Visits vendors on a regular basis to maintain up-to-date information on the production status, quality levels and ensures understanding of Company 's QA requirements. • Provides merchandising staff with accurate evaluation of quality performance of the manufacturers. • Prevents quality and production problems by reviewing options and taking action to ensure standards are met. • Creates inspection plans to ensure that all phases of inspection are completed in timely manner. • Assigns inspection schedules to each QA Auditor on a weekly/monthly basis and reviews the workload of each. • Assists the QA Auditors with their daily inspection workload. • Assists the QA Manager with control of the inspection expenses • Supervises and motivate the subordinates • Control customer complain and customer services • Receiving customer complaints, cooperate with relevant departments to find the root cause, corrective action reports for customers.Receive and control return products from customers • Control calibration all electronic on factory • Document control and issue document for relevant section • Control with customer about quality requirement • Prepare, review and approval procedure, work instruction, form and training to production/ QC • Daily monitoring production/material quality, lead the quality meeting with relevant section 2015 – Present : NARIS COMETICS Viet Nam, Binh Duong City Position: QC Manager • Manage all activities related to the microbiological needs of new project teams. Cross functional teams. Advise team leader/management of resources needed to accomplish tasks. • Manage QC testing and Deviation/NCR personnel to ensure routine manufacturing operations are monitored and controlled and all required materials and end products are assessed and meet specifications. • Manage contract lab activities and testing. Determine incoming Raw material and final product disposition based on regulations requirements. Serve as the liaison between all QC laboratories and other internal/external functional areas. • Lead qualification studies to establish in house capability for microbiology testing, and microbial identification. Lead validations of all instruments used in all labs. Train laboratory personnel on the Operation and maintenance of standard laboratory equipment. • Lead laboratory microbiological investigations. Determine root cause and implement corrective actions identified from investigation. Work with Quality Engineers for NCR/Deviations in the root cause analysis of non-conformances and other failures; initiate, implement Corrective Action/Preventive Action (CAPA) and monitor for effectiveness. • Develop, review and revise laboratory Standard Operating Procedures. Write study protocols, reports, test procedures etc. Compile data and prepare summary reports as needed.