QA Analyst (Entry Level) - Nhân viên QA

Công Ty TNHH Dược Phẩm Quốc Tế UIP

497

Hạn nộp hồ sơ :

07/01/2021

THÔNG TIN

VIỆC LÀM CÙNG CÔNG TY

CÔNG TY

MÔ TẢ CÔNG VIỆC

Establish and implement all procedures related to control document, comply with WHO-GMP, PIC/s, ISO and OHSAS requirements.
Make sure that all quality, environmental and safety– impacting procedures are available and effectively implemented.
Review all documents as SOP, artwork, protocol, process,... before approval.
Assist Document Controll Supervisor to provide technical data and coordinate with Regulatory Affairs personnel on product registration and other regulatory requirements.
Type the procedures, document of the department.
Comply with safety rules and regulations and actively participate in activities on safety and environmental aspects of the company.
Manage and improve documentation processes, storage, and safekeeping in the factory. Drive compliance to Good Documentation Practices (GDP) in the factory. Ensure that all documents are accurate, up-to-date, and truthful at all times.
Support Operational Excellence (OE) programs in the Quality Assurance Systems Department.
Performs other duties and responsibility as may be assigned from time to time.