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Đinh Minh Hoàng's picture

Đinh Minh Hoàng

Android HD+ Producer at Gameloft VN
Da Nang (Vietnam) - 20 connections

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Overview

  • Current:
    Android HD+ Producer at Gameloft VN
  • Past:
    • Quality management manager at SODI- Vietnam (non-government, non profit and humanitarian organization
    • GMP expert of Pymepharco for EU-GMP project at Pymepharco, Phu Yen province
    • Liaison officer in Vietnam at Tangenttech infosoft Pvt., company
    • QA engineer and technical deputy director's assistant at Stada -VN
  • Education:
    • Dai hoc Su pham Ky thuat TpHCM, Vietnam
  • Connection:
    20 connection(s)

Summary

I have worked and experienced in quality management system. I always want to learn and face higher challenges in quality management field

  • Job Function:
  • Industries:
    Pharmaceutical/Biotech, NGO/Non-profit
  • Specialities:
    Quality management system: ISO 9001-2008, WHO GMP, EU-GMP. GSP, GEP
  • Job Level:
    Manager

Experience

  • Android HD+ Producer

    Gameloft VN
    October 2013 - Present (6 years 2 months)

    In Gameloft, we are producing the Android HD Games. My job is a producer who has main responsibility to keep a Game producing project being able to finish on time and with the highest quality as design

  • Quality management manager

    SODI- Vietnam (non-government, non profit and humanitarian organization
    August 2012 - October 2013 (1 year 2 months)

    - Establish, monitor and maintain the Quality management system to comply with ISO 9001:2008
    - Monitor and handle all quality reports of system
    - Analyse all quality reports of system to propose the appropriate CAPAs in time if necessary
    - Monitor whole quality management system to ensure the continuous improvement
    - Conduct internal audit and control within system
    - Liaise the stakeholders regarding to quality management
    - ensure the connection of the finance management system to quality managment system, conduct frequently finance internal audit
    - Establish, monitoring and maintain the performance management system (KPIs system)
    - propose and consult top management regarding to quality management system
    Achievement:
    - Succeeded getting ISO 9001:2008 certificate from BSI within 3 months for two projects in Hue and Quang Tri province
    - Established and implement the Finance management system and performance management system of program level, succeeded linking these systems to QMS

  • GMP expert of Pymepharco for EU-GMP project

    Pymepharco, Phu Yen province
    November 2011 - February 2012 (3 months)

    - Review and rearrange GEP (good engineering practices) system of engineering department: Utilities (HVAC, Purified water, water for injection, boiler, compressed air, nitrogen system); manufacturing equipment for both validation, revalidation, qualification and maintenance. Review and upgrade all SOPs system as per EU-GMP. Monitoring and ensuring the compliance of all staff members of engineering departments
    - Review and rearrange GMP system of production department: all SOPs system reviewed and upgraded as per EU-GMP; Set up procedure for performing process validation, cleaning validation, report for process validation; Training PICs; Review equipment validation and cleaning activities. Check all storage condition of beginning materials and intermediate material, finished goods.
    - Review and rearrange GLP system of quality control department: all SOPs system reviewed and upgraded as per EU-GMP; Review and ensure all analysis and analysts for implementation of SOPs. Checking all sampling testing, storing and handling as per SOPs. All validation, qualification, training activities are reviewed and fixed up. All micro-lab activities are reviewed: environmental monitoring, PW monitoring as per EU-GMP
    - Review and rearrange GSP system of warehouse department: all SOPs system reviewed and upgraded as per EU-GMP; Perform temperature and relative humidity mapping for all storages; Set up the alarm systems of warehouse for temperature and humidity conditions. Check all storage conditions of all beginning materials, Finish products; dispensing activities as per EU regulars
    - Set up and enhance the abilities of QA department: upgrade training procedures and systems for all departments; Make Risk assessments and CAPAs accordingly; Arrange and perform all annual monitoring and validation for utilities systems and environmental and manufacturing processes. Ensure the calibration activities to be complied in all departments of GMP systems
    - Set up pest control program, laudry area checking, health check, personal hygiene check as per EU-GMP
    - Perform internal audit and reports with CAPAs.
    - Perform upgrade training, on job training for all departments about the concerned activities
    - Take care 2 pre audits from STADA-AG
    - Take care official audit from Drug authorities of German
    - Perform CAPAs report of all audits and monitoring the compliance activities
    Achievements:
    - Successes in Audit case from: EU-GMP

  • Liaison officer in Vietnam

    Tangenttech infosoft Pvt., company
    October 2010 - October 2011 (1 year)

    - Specialize in consulting for pharmaceutical company in building up and maintaining the current GMP system
    - Consultant and development for automation solutions, SCADA, PLC, monitoring and controls systems and softwares for all enterprises and factories in all industrial fields
    - Support STADA-VN for WHO international GMP audit from July to end of August, 2011
    Achievements:
    - Successes in Audit case from: WHO international GMP

  • QA engineer and technical deputy director's assistant

    Stada -VN
    July 2007 - September 2010 (3 years 3 months)

    o 07-11/2007: staff member of quality assurance (QA) with translating responsibility, detail:
    • Translate all technical documents of machine: validation documents (installation qualification, operation qualification), technical documents (operation manual), standard operating procedures
    • Translate in period time of machine validation between operators, engineers and foreign service experts from suppliers from different countries (Germany, India, China, Sweden, Korea)
    • Compose validation document and in charge of change parts, equipments validation as QA member in validation team (production, QA, engineer and supplier)
    o 11/2007-9/2010: Assistant to Deputy Director- technical (DDT) (Indian expert) and QA engineer concurrently, with main duties:
    • Continue with all above duties
    • Follow all instructions of DDT in the last period of time of project (from July- Dec, 2007, STADA completed all construction project of new factory and GMP audit as per EU-GMP), including:
    • Carry out, build up and implement the quality system for warehouse: raw material, packing material, finished goods stores as per GSP standard
    • Carry out, build up and implement the quality system for engineering department: validation documents, checklist, monitoring documents, deviation reports, maintenant documents, revalidation, qualification documents as per GEP standard
    • Carry out, build up and implement the quality system for Quality control department
    • Making internal Audit and report to DDT all GMP implementation procedure of manufacturing areas as per GMP standard
    • Coordinating for all concerned departments and DDT
    • After finished above projects, continue with new duties:
    • Main person in carrying out new projects as per DDT’s instructions, such as: Project of Computerised validation for all system and instruments of factory; Project of ERP system applied to warehouse management
    • Communicating and coordinating with partners and suppliers in concerned fields
    • Arranging business trips for DDT and coordinate with concerned departments
    • Interpreting all meetings between DDT and employees
    • Monitoring, reporting the progress of jobs in manufacturing, engineering, quality department
    • As a main member of internal audit group
    • Welcoming and presenting about company to partners, guests (local and foreigners)
    • Main member of GMP group in working with inspection groups
    • Main interpreter of all audits from oversea organizations
    Achievements:
    - Best performance in two years: 2007-2008, 2008-2009
    - Successes in Audit cases from: GMP-EU, GMP-Taiwan (PIC/S), GSK Audit

Education

  • Dai hoc Su pham Ky thuat TpHCM (Vietnam)

    Bachelor of Engineering , printing technologies
    2002 - 2006

Training/Certificate

  • Key performance management

    2013

    Trained by Apave VN about how to set up, implement, monitor and appraise the key performance management system from high level to base level

  • Financial management system

    2013

    Trained by KSi VN about how to monitor the financial management system

  • ISO 9001-2008 Quality management system

    2012

    Trained by APAVE VN about how to build-up, implement, monitor and develop the ISO 9001-2008 QMS

  • Quality management as GMP EU standard

    2008

    Trained by STADA-AG, HQ in Berlin of STADA VN.

  • computer Aid desig technician

    2003

    training the technician level in design with computing software aids

Additional Information

  • Websites:
  • Groups and Associations:
  • Honors and Awards:
    Achievements:
    - Best performance in two years: 2007-2008, 2008-2009
    - Successes in Audit cases from: GMP-EU, GMP-Taiwan (PIC/S), GSK Audit
    - Succeeded getting ISO 9001:2008 certificate from BSI within 3 months for two projects in Hue and Quang Tri province
    - Established and implement the Finance management system and performance management system of program level, succeeded linking these systems to QMS
    - Continuous Gold the projects in gameloft

Personal Information

  • Hobbies and Interests:
    reading book, singing Karaoke, watching film
    Playing badminton, walking on the beach

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