Responsibilities:
1. Support manager to maintain the quality management system for China local commercial organization to comply with China GSP regulations and Corporate Quality Management System.
2. Assist in organizing, archiving, and updating Quality Management System documents for Greater China region.
3. Work closely with cross-functional team to create, maintain and continual optimize China local SOP documents to meet with GSP regulation and business needs.
4. Conduct quality surveillance of customer license, vendor license and product.
5. Update the changes of NMPA regulations on medical device distribution to China business team and provide support on warehouse management.
6. Assist in staff training and education on regulation and quality system and track the completion of the training.
7. Other duties assigned by manager.
Qualifications:
● Currently pursuing a Bachelor's or Master's degree in Pharmacy, Biology, Medicine, Biomedical Engineering, Quality Management, or a related field.
● Strong interest in the medical device or pharmaceutical industry, with a willingness to learn and develop in the field of quality management.
● Meticulous, detail-oriented, with a strong sense of responsibility and a rigorous work ethic.
● Good communication skills and a team player.
● Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).
● Good English reading and writing skills.