Mô tả công việc

• Management the change control, deviation, supplier management Compile and update CGMP documents, including work instructions, SOPs, product master files, master batch records...

• Train basic CGMP.

• Support in investigating and handling abnormalities complaint products, returned products.

• Support coordinating with other departments to audit suppliers and/or approve on-site.

• Control document for releasing product

Yêu cầu ứng viên

• 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