Job Description

GQP Compliance Group, as Quality Assurance Department, contribute to business by concluding appropriate quality agreements with suppliers such as pharmaceutical manufacturing sites, we provide an environment where the Quality Assurance Department can smoothly interact with suppliers, contributing to the stable supply of high-quality pharmaceuticals to patients.

Using expertise in GQP and GMP regulations, as a Quality Assurance professional, this position would manage following tasks

Be responsible for concluding and revising quality agreements and quality contracts with domestic and international manufacturers, and perform appropriate GMP management tasks.
Perform document management tasks related to GQP ordinances (creation and revision of SOPs).
Execute or oversee other tasks related to quality assurance.

Required Skills and Knowledge

BA degree or above in Science
Over 5 years of experience in QA/QC within the pharmaceutical industry, specifically related to GQP/GMP/GDP.
Practical experience in negotiations and dealings with external manufacturers and suppliers, including those overseas.
Experience in agreements, contracts, and document management tasks.