หน้าที่ความรับผิดชอบ

Responsibilities:

– Ensure Document Control system of the company are in compliance with GMP Standards.
- Review SOP/WI /Form of all departments to ensure all documents align with GMP.

- Ensure quality records of Quality Documentation (QD) team are kept according to retention period.
– Audit handing and formulating replies for deficiencies and suggesting CAPA with the Quality and Production pharmacist.

- Participate in a project pertaining to process related Quality System procedures to ensure that the new implementation comply with the company policy, quality manual, and standard procedures.
- Liaise with the Certified Body for GMP Certification /Surveillance Audit.