1. Manage the overall quality assurance related activities
2. Manage local batch release procedure and vendor QC laboratories
3. Review internal quality status about pharmaceuticals devices and maintain its compliance according to domestic regulations
4. Monitor the progress of KFDA audit and CQA audit in Korea
5. Manage the deviation and related CAPA during QA activities
6. Support GMP site inspection abroad for registration of our products
7. Implement CQS and Global Procedures in accordance with defined timelines

1. Bachelor’s Degree(Pharmacy)
2. Pharmacist
3. More than 2~3 years experience in Quality Assurance
4. Product knowledge of regulations and its requirements
5. Fluent in English

- 원서 마감후 1차(서류) 합격자에 한하여 개별연락
- 이력서에 연락처, 희망연봉 게재
- 해외여행에 결격 사유가 없는 자