DINH VU LONG GIANG

Experience

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  Olympus

  May 2008 - Jan 2016

  QA Manager

  My responsibilities include: ① Establish and implement the quality management system for the production of medical devices (ISO 13485:2003). ② Management sterilization process for endoscope, in accordance with ISO 11135:2007. Make a work plan for sterilization group. ③ Management packing process, in accordance with ISO 11607 – 1 : 2006, ISO11607 – 2 : 2006. ④ Management Cleaning Room in accordance with ISO 14644 – 1 : 1999, ISO 14644 – 2 : 2000, ISO 14644 – 3 : 2005, ISO 14698 – 1 :2003. ⑤ Responsible for Validation Sterilization Process. ⑥ Responsible for Packing Process, validation cleaning room. ⑦ Responsible for quality of product in sterilization process and product after sterilize. ⑧ Responsible for managing the accuracy of measuring instruments ⑨ Contacting and handling trouble occurred in house and customer complaint ⑩ Responsible for training with staffs about knowledge related to operations. ⑪ Leader 5S in Medical Division. ⑫ Establish and implement the environment management system (ISO 14001:2009). ⑬ Trouble handling and improvement ⑭ Responsible for internal quality audit and external audit for environment system. ⑮ Other Mas kaunti

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  Terumo BCT

  Jan 2017 - Jan 2022

  Quality Engineer Manager

  Job Summary: Supervising Quality engineering team to allocate detailed engineering work on a projects or routine tasks to experienced engineers. Duties are assigned to provide experience and familiarization with engineering methods, independent thinking, and company practices and policies.Essential Duties:1. Manages and provides guidance for the Quality Engineering group development, effectiveness, adhering to organizational policies and processes and supporting overall business and corporate targets.2. Serves as expert and main point of contact for Quality issues within area of responsibility (In-process, Quality System, EtO sterilization system, Steam sterilization system, NC/CAPA system, Calibration system…)3. Influences the organization in quality objectives, prioritization and resourcing decisions as necessary.4. Acts as an internal key contributor for quality initiatives aimed at improving product quality, business systems and compliance; may be the primary representative of Quality group on projects.5. Responsible for the project and or work group expenditures vs. plan6. Ensures compliance with Quality System regulations and safe working practices (FDA’s regulatory, ISO 13485, ISO11135…) 7. Plans, guides, and reviews projects and or work groups under one’s control to produce the desired outcome.8. Utilizes technical skill to evaluate proposed solutions, adaptations, and modifications to projects. Mas kaunti

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  Nidec Servo Corporation

  May 2017 - Jan 2017

  Quality Manager

  Responsible works:1) Establish and implement the quality management system for the production of Oto component (ISO 16949 : 2016)2) Ensures compliance with Quality System regulations and safe working practices (ISO 16949, ISO9001…)3) Responsible for managing the accuracy of measuring instruments4) Contacting and handling trouble occurred in house and customer complaint5) Trouble handling and improvement6) Responsible for internal quality audit and external audit. 7) Serves as expert and main point of contact for Quality issues within area of responsibility.8) Other Mas kaunti

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  Zettler Vietnam

  May 2021 - now

  • Factory Manager at ZETTLER VIETNAM

    Jan 2023 - now

  • Quality Engineer Manager

    May 2021 - Jan 2023