CHUYÊN VIÊN QC (HÓA LÝ) / PHYSICO-CHEMICAL SUPERVISOR

Mô tả Công việc

1. Preparation/ review documents (80%)

• Responsible for preparation/ review of documents such as but no limited: SOPs, specifications, testing procedures, analytical datasheets, trend analysis, risk assessment, etc.
• Preparation of User Requirements Specification, operating & cleaning procedure, documents for calibration/ validation/ qualification/ maintenance, monitoring the qualification and calibration status of equipment.
• Preparation of protocols for method validation and conducting tests for analytical method validation based on the protocol.
• Preparation of protocols for stability study and evaluate, monitor the stability sample of the product under study.
• Test raw materials, intermediate products, bulk products and finished products.

2. Other works (20%)

• Following instructions and reporting directly to the Head of QC department
• Taking other tasks which are assigned by the Head of QC department

Yêu Cầu Công Việc

- Education: Bachelor’s degree in chemical or pharmaceutical sectors

- Experience: Preference will be given to candidates with experience in pharmaceutical industry, especially EU GMP factory.

- Skills:

•  English: Reading comprehensive documents in the pharmaceutical sector, good at communication and writing skills
• Office skills: Effectively using office applications including Word, Excel, PowerPoint, etc.
• Others/Khác: be active in tasks, self-studied, and friendly with colleagues.