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Mô Tả Công Việc
1. Knowledge of quality management systems.
2. Knowledge of ISO 13485, PLM is a plus.
3. Control of documents and quality records following Quality System requirements.
4. Be in charge of Audit, CO, NC, CAPA, etc.
5. Prepare and complete registration records according to regulatory affair requirements.
6. Analysis data and prepare periodical reports, plans.
7. Manage pre-shipment inspection activities and ensure records are accurate and ready for each shipment.
8. Perform other assignments as requested.
Yêu Cầu Công Việc
1. Bachelor’s degree or higher
2. Have at least a minimum of two years working experience in quality.
3. Experience in ISO and/ or medical device industry would be advantage.
4. Computer skill: Proficient in Excel, Word, and MS Office/PC applications.
5. English skills: Good command of English (written & verbal) and able to translate well from Vietnamese into English & vice-versa
6. Be detail-oriented, dependable and trustworthy since this position come in contact with complex and sensitive documents.
Hình thức
Quyền Lợi
- Attractive salary
- Excellent growth and advancement opportunities
- Great working environment
Mức lương
Thỏa thuận
Tham khảo: 10 Dấu hiệu nhận biết hành vi lừa đảo qua tin tuyển dụng.
