蕊 王
Regulatory Affairs Director @ SceneRay
China
Suzhou
Medical Device
FDA GMP, ISO 14971, 21 CFR, ISO 13485, Japanese, 法规事务, 质量体系, CAPA, 标准作业程序, 监管分析, Disinfectant Product Filing and manufacturing site health permit, Drug formulation and process development, 上市前批准, 药品生产质量管理规范, 认证质量审核员, 医疗器械法规
Experience
Regulatory Affairs Director
SceneRay
Design Quality and Regulatory Affairs Senior Manager
Genesis Medtech Group
常州-无锡-苏州地区
Senior RA Manager
Genesis Medtech Group
中国 江苏省 苏州
RA Manager
Reckitt
Suzhou
Medical Device
Registration Manager
Smith+Nephew
Suzhou
Technical Project Leader
Smith+Nephew
Suzhou
China Domestic Products Induction Projects
高级研发工程师
Santen
Suzhou
Education
Shenyang Pharmaceutical University
Pharmaceutical
蕊 王's Contact Information
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