职位描述
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罗氏促进多元化、公平性和包容性,代表我们所服务的社区。在全球范围内处理医疗保健问题时,多元化是成功的关键因素。我们认为,包容性是理解人们不同医疗保健需求的关键。我们共同拥抱个性,共同抱持对卓越护理的热情。加入罗氏,每个声音都会得到重视。
职位
You will be responsible for:
*
Establishing and maintaining the good and closed relationship with CFDA
testing centers. And successfully gains product registration certificates per
registration forecast plan.
*
Establishing and maintaining the good and closed relationship with hospital
IVD departments (clinical Lab, drug monitoring lab, GCP, etc…). And building up
and represents Roche Diagnostics’ good image, and gain products clinical trial
reports per action plan.
*
Monitoring and reporting on local regulation changes and its impact together
to company.
*
Assisting manager to handle daily work in Regulatory Dep.
*
Working with sales and marketing dep. to fulfill product registration plan.
Achieves RD expectation on product registration.
*
Establishing and maintaining the good relationship with key contacts.
Recommends valuable suggestion to company
*
As a member of RD, providing active and strong regulatory supports to internal
dep. as needed.
*
Initiatively dealing with daily works, keeping records. Has clear filing and
maintain of all documents.
*
Other projects or tasks assigned by line manager
*
Conducting business in full compliance including but not limited to Roche
Secure, Roche Behavior in Business, Roche Competition Law Interactive
Dialogues, Roche Safety, Security Health and Environmental Protection
You should have:
*
Bachelor degree or above, subject on Medical/bioengineering/ clinical Medicine
or biochemistry .
*
Have not less than 2 years about experience in medical regulatory affairs,
focus on testing center and clinical trial. Understand IVD products’ Standard
like industry and national standards (YY and GB)
*
Medical laboratory background.
*
Familiar with medical device regulation.
*
High enthusiasm and devotion, work hard and earnest
*
Willing to work under pressure, self-starting and self-inspiring
*
Be honest and open, excellent interpersonal communication skill, ability of
social activity and collaboration
*
Innovating with good independent working ability
*
Energetic team spirit
*
Fluent English in listening, speaking and written.
*
Good skill on computer, MS-Office operation.
我们是谁
在罗氏,来自100个国家的100,000名员工不断推动着健康医疗行业的进步。我们一同工作,使罗氏成为了世界领先的以研发为基础的健康医疗集团。我们的成功源于创新、求知和多元化,也源于我们把相互间的差异作为一种优势。为了革新医疗健康领域,罗氏设定了远大的计划,坚持学习和发展,并不断寻找与之志同道合的伙伴。
罗氏提供平等的职业发展机会。
职位
You will be responsible for:
*
Establishing and maintaining the good and closed relationship with CFDA
testing centers. And successfully gains product registration certificates per
registration forecast plan.
*
Establishing and maintaining the good and closed relationship with hospital
IVD departments (clinical Lab, drug monitoring lab, GCP, etc…). And building up
and represents Roche Diagnostics’ good image, and gain products clinical trial
reports per action plan.
*
Monitoring and reporting on local regulation changes and its impact together
to company.
*
Assisting manager to handle daily work in Regulatory Dep.
*
Working with sales and marketing dep. to fulfill product registration plan.
Achieves RD expectation on product registration.
*
Establishing and maintaining the good relationship with key contacts.
Recommends valuable suggestion to company
*
As a member of RD, providing active and strong regulatory supports to internal
dep. as needed.
*
Initiatively dealing with daily works, keeping records. Has clear filing and
maintain of all documents.
*
Other projects or tasks assigned by line manager
*
Conducting business in full compliance including but not limited to Roche
Secure, Roche Behavior in Business, Roche Competition Law Interactive
Dialogues, Roche Safety, Security Health and Environmental Protection
You should have:
*
Bachelor degree or above, subject on Medical/bioengineering/ clinical Medicine
or biochemistry .
*
Have not less than 2 years about experience in medical regulatory affairs,
focus on testing center and clinical trial. Understand IVD products’ Standard
like industry and national standards (YY and GB)
*
Medical laboratory background.
*
Familiar with medical device regulation.
*
High enthusiasm and devotion, work hard and earnest
*
Willing to work under pressure, self-starting and self-inspiring
*
Be honest and open, excellent interpersonal communication skill, ability of
social activity and collaboration
*
Innovating with good independent working ability
*
Energetic team spirit
*
Fluent English in listening, speaking and written.
*
Good skill on computer, MS-Office operation.
我们是谁
在罗氏,来自100个国家的100,000名员工不断推动着健康医疗行业的进步。我们一同工作,使罗氏成为了世界领先的以研发为基础的健康医疗集团。我们的成功源于创新、求知和多元化,也源于我们把相互间的差异作为一种优势。为了革新医疗健康领域,罗氏设定了远大的计划,坚持学习和发展,并不断寻找与之志同道合的伙伴。
罗氏提供平等的职业发展机会。
工作地点
地址:上海闵行区虹桥天地2号楼
查看地图
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职位发布者
HR
罗氏诊断产品(上海)有限公司
![](http://img.jrzp.com/jrzpfile/provincercw/images/sfrz_yrz.png)
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制药·生物工程
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500-999人
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外商独资·外企办事处
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申长路900号虹桥天地2号楼