China Regulatory Affairs operation Trainee
爱尔康（中国）眼科产品有限公司
- 公司性质：外资(欧美)
- 公司行业：医疗/护理/卫生
职位信息
- 发布日期：2016-09-17
- 工作地点：北京-朝阳区
- 招聘人数：1人
- 语言要求：英语 熟练
- 职位月薪：4500-5999/月
- 职位类别：药品注册
职位描述
职位描述：
Major Accountabilities
·Responsible for supporting regulatory submission for all new products and life cycle management of marketed products in China, aligned with Regional regulatory and Area business strategies and plans for VC business.
·Support the consolidation of regulatory filings to ensure we are fully compliance.
·Maintain the Insight and D2 systems and any other regulatory systems.
·Update and Maintain China Regulatory Affairs Sharepoint site.
·Track the RIAR activities in China.
·Support any regulatory affairs administrative activities.
Ideal Background
Education / General
University degree or equivalent in biomedical field and higher degree with no experience in Regulatory Affairs required. Good command in English for both oral and written.
Expertise/Experience/Skills
?Some knowledge of the regulations affecting the Pharmaceutical and medical device industry in Area; including both pre-market and post-approval regulations. A working knowledge of regulatory review and approval processes in other global markets
?Action oriented with proven ability to move projects through to approval and commercial success.
?High energy, hands-on individual with a collaborative personal style and the ability to work well in a team environment.
?Transparent communicator..
举报
分享
Major Accountabilities
·Responsible for supporting regulatory submission for all new products and life cycle management of marketed products in China, aligned with Regional regulatory and Area business strategies and plans for VC business.
·Support the consolidation of regulatory filings to ensure we are fully compliance.
·Maintain the Insight and D2 systems and any other regulatory systems.
·Update and Maintain China Regulatory Affairs Sharepoint site.
·Track the RIAR activities in China.
·Support any regulatory affairs administrative activities.
Ideal Background
Education / General
University degree or equivalent in biomedical field and higher degree with no experience in Regulatory Affairs required. Good command in English for both oral and written.
Expertise/Experience/Skills
?Some knowledge of the regulations affecting the Pharmaceutical and medical device industry in Area; including both pre-market and post-approval regulations. A working knowledge of regulatory review and approval processes in other global markets
?Action oriented with proven ability to move projects through to approval and commercial success.
?High energy, hands-on individual with a collaborative personal style and the ability to work well in a team environment.
?Transparent communicator..
职能类别： 药品注册
公司介绍
爱尔康成立于1945年，目前总部位于瑞士日内瓦。作为眼健康领域的引领者，自成立以来一直专注于视力健康，致力于为全球140多个国家和地区的人们带来更好的视觉体验。
爱尔康于1995年成立中国公司，致力于为国内眼科专家、患者和消费者提供更好的解决方案。爱尔康中国不仅提供创新的产品和服务，还竭诚为国内眼科医生打造国际化的学习交流平台，积极推动中国眼科事业的发展。此外，企业还同眼科基金会等慈善机构紧密合作，支持各类扶贫项目，为中国的防盲治盲工作贡献力量！
2019年4月，爱尔康在瑞士证券交易所和纽约证券交易所同步上市。企业持续秉承对客户、患者和消费者的承诺，通过引领眼科及视力保健产品的突破性创新改善视觉质量，提升人们的生活品质，与大家一道共见精彩！
爱尔康于1995年成立中国公司，致力于为国内眼科专家、患者和消费者提供更好的解决方案。爱尔康中国不仅提供创新的产品和服务，还竭诚为国内眼科医生打造国际化的学习交流平台，积极推动中国眼科事业的发展。此外，企业还同眼科基金会等慈善机构紧密合作，支持各类扶贫项目，为中国的防盲治盲工作贡献力量！
2019年4月，爱尔康在瑞士证券交易所和纽约证券交易所同步上市。企业持续秉承对客户、患者和消费者的承诺，通过引领眼科及视力保健产品的突破性创新改善视觉质量，提升人们的生活品质，与大家一道共见精彩！