Job Description :

• 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 ...