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QA Assistant

Pharmaceutical/Medical

Ho Chi Minh

Negotiable

•    Responsible for document record & archive management in whole project.
•    Control the qualification documentation provide by the contractor: facility qualification; utility URS, DQ, IQ, OQ; process equipment URS, DQ, IQ; computerized system validation, process validation, cleaning validation; participate and follow the test done by the different supplier.
•    Transfer SOPs from current factories to ACE and prepare SOPs necessary for GMP certification stage.
•    Fluently answer to the phone in English and Vietnamese.
•    Organize the Agenda, send the courier and organize the archive of the project
•    Assist the deputy to establish the qualification/ validation, documentation archives and procedure

•    University degree in Engineer of Science or Pharmacist
•    At least 2 years working in Quality/Production in Industrial factory applied GMP (Cosmetic or Pharma)
•    Fluent in both Vietnamese and English
•    Good computer literacy
•    Able to organize the time according to the work.
•    Readily adapts to new environment, jobs, technologies, processes
•    Strives to build mutually beneficial solutions and partnerships

 

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