Workplace: Lot 18-4, 18-5, Road 3B, Protrade International Industrial Park, Tay Nam Ward, Ho Chi Minh City, Vietnam (Binh Duong)
Control validation activities and cooperate with related departments in validating manufacturing and cleaning processes.
Compile and issue Batch Manufacturing Records (BMR) based on master documents.
Control and maintain documentation; compile and update work instructions and SOPs.
Supervise and evaluate the handling results of production deviations.
Cooperate with other departments to evaluate change proposals.
Cooperate with other departments in investigating and handling product complaints and recalls.
Promptly report any abnormalities and factors that may affect product quality, as well as issues related to the quality of materials and finished products, to the Head of Department and related departments.
Perform other duties as assigned by the
QA Manager.
Graduated from University (major in Biotechnology, Chemical, Pharmacy or related discipline)
Microsoft Office skill (Word, Excel, PPT)
Can communicate in English (Reading, Writing and Speaking)
Teamwork skills
Problem-solving skills
Working under pressure
Careful, honest
Strong and good discipline