RA Associate Manager_电生理

职位描述


product registration related including new and renewal
handing registration process for S1/2 including document requirement dossier prepare, submit to CFDA, Follow up evaluation procedure, sample ordering type testing, solve various problems in whole process, file dossiers with consistent requirement;
Ensure to obtain the regulatory permits on time, in support of the organization's business plan especially product launch plan;
Establish working relationship with officials and experts in authorities, good communication and negotiation with officials and experts to guarantee smooth registration;
Pay attention to the market information such as the competitors with the analysis;
To coordinate the post surveillance project.

资历
Medical or related education background and knowledge;
3-5 years medical device experience in regulatory affairs
good communication skills;
Good time management skills;
Well computer operating;
Better English and Chinese in Writing and oral

主要地点
中国-北京-北京-
组织
强生(上海)医疗器材有限公司
工作
Regulatory Affairs
Requisition ID
1905779982W