法规注册（双休）

职位类别： 医疗器械注册

技能:Skills
1.rich experience in literature search in databases are preferred.
2.successful experience with clinical Eation for MDR
3.Good ability to search incidents and recalls from foreign websites such as FDA MAUDE.
4.Demonstrated in the active medical device regulatory standards and skillful in the standards with respect to the electrosurgical insturments. 
职责范围：
1. work with product development team to perform  product clinical research for MDR registration
2. develpment and update the clinical information for marketed product.
3. Perform post market clinical follow-up studies for marketed products.
4.Update post production information for marketed products.
5. Update Regulatory and standards(FDA, Health Canada , EU) information every month.

• 年龄要求： 不限
• 语言要求：不限