1. Support RA project owner maintain current NMPA approved certificates, including extension registration, change registration and support BU&RC to resolve post-marketing issues.
2. Support RA project owner on new products launch in China, including, type test, prepare registration documents, etc..
3. Host regular meeting with WW to get requested documents and update registration status.
4. Other affairs within the team.
SKILLS AND ABILITIES（技能）
1. Medical/Pharmacy background, or relevant experience on regulatory affairs
2. Bachelor degree or above
3. Proficient in spoken and written English and Chinese
4. Excellent interpersonal and communication skills
DESIRABLE（优先条件）
1. Knowledge of MS-office systems
2. Medical device company working experience.
3. Overseas education background
职能类别：医疗器械注册
关键字：pharmacyregistrationmedical医学医疗器械法规注册法规事务
英语良好