FITOPHARMA PHARMACEUTICAL COMPANY LIMITED
Quality Assurance (QA) Department Staff
DOCUMENTATION AND ASSESSMENT RESPONSIBLE JOB DESCRIPTION
JOB DESCRIPTION
-Compile necessary documentation for GMP factory activities.
-Plan and execute assessments according to the original VMP assessment plan.
-Coordinate with relevant departments for assessment support.
-Propose re-assessments when necessary.
-Monitor and support activities of other departments.
-Maintain records in the Quality Assurance Document system.
Requirements:
-Bachelor’s degree or higher in Pharmacy.
-Experience working in QA department related to GMP supervision, assessment, documentation, and reporting.
-Strong analytical and process development skills, understanding of Quality Management System is an advantage.
-Salary: Negotiable (Based on qualifications).
Location: QL13, Vinh Phu, Thuan An, Binh Duong.
Working Hours: 8:00 AM – 5:00 PM from Monday to Friday. Half-day on Saturday.
CV Submission Information: Ms. Phuong Nhi – Email: nhi@fito.vn – Phone: 0933.033.931