I am looking for a job opportunity due to my contract was finished last Nov. 2019 in Macao as a Validation Officer in a Pharmaceutical Manufacturing. I have more than 7 yrs. of working experience in Manufacturing Industry. I am available for immediate deployment.


  • Validation Officer

    at Ashford Laboratories Ltd.

    January 2018 - at Present

    Concelho de Macau

    In-charge in managing validation and qualification projects of the company involving Process, Test Method, Cleaning, Equipment, Facility, Utilities and Computer Systems. Ensure full compliance with the relevant regulations, guidelines and requirements, along with health and safety standards. Authored and maintain validation deliverables, such as master plans for different validation areas, protocols and reports, as well as the test procedures, standard operating procedures, summary reports and traceability matrices. Aligns validation activities with audit findings to improve the overall quality and value of the validation activities. Refers to technical dossiers and international standards and strives to keep the Manufacturing Plant abreast with the latest validation standards/ strategies and best practices. Conduct product development and reformulation if deemed by the management. Conduct supply audit and internal quality audit if deemed by the management.

  • Validation Technologist

    at Interphil Laboratories Inc.

    September 2015 - January 2018


    In-charge in Non-process validation activities and prepare protocols and reports of Equipment, Facility, Utility, Cleaning and Computer in Plant 1 and Plant 2. Supervises the conduct and implementation of the non – process validation activities (IQ/OQ) in compliance to pre – approved validation protocols, Standard Operating Procedures (SOP’s) and cGMP. Performs contingent tasks related to or arising from the validation activity, such as but not limited to: a. Preparation of Deviation Reports, Change Notification Forms and Investigation Reports. b. Recommendation on revisions to SOP’s. c. Technical presentations to Validation Department or Technical Committee. d. Final turn – over to process owners.

  • Quality Assurance Specialist

    at Grand Alpha International Corp.

    August 2014 - September 2015


    Train, educates and supervise personnel on the production and Quality department in implementing strict Good manufacturing practices and Standard Operating Procedures as predetermined in the Quality Systems Manual. Determine overall plant product quality by conducting and evaluating various product tests and tests related to ingredients and packaging. Discuss plant evaluation with plant management, make appropriate recommendations and set timetable for improvement and corrections and prepare plant evaluation reports and submit them to manager, quality assurance Services.

  • Quality Assurance Analyst

    at Ginebra San Miguel Inc.

    June 2012 - August 2014


    Trains and supervise bottling personnel before and after deployment inside the production area. Inspect and conduct quality testing of Liquor by Physico-Chemical Analysis of In-Process and finished goods. Collates, reviews and analyze all production data and laboratory test results for proper generation. Ensures, monitor and supervise that all activities are executed inside the production area complies with the approved Standard Operating Procedures and Good Manufacturing Procedure (GMP).


  • Intermediate Mandarin Chinese

    at University of Macau

    2019 - 2019 (1 year) Concelho das Ilhas

  • Elementary Mandarin Chinese

    at University of Macau

    2018 - 2018 (1 year)

  • Bachelor of Science in Biology

    at New Era University

    2008 - 2012 (4 years) National Capital Region

Services offered

  • Validation

    All types of Validation such as the following:
    Test Method

  • Quality Assurance

    Quality Systems

  • Quality Control

    Laboratory Testings


  • Tagalog Native

  • English Native

  • Chinese Conversation