苏州招聘

职位描述：
Qualification
  任职资格
1.Medical Device regulation experience or background is compulsory
2. Minumum 5 years working experience
3. Initiative attitude
4. Smart enough to study the new regulations.

Main Responsibilities
主要工作职责
1.Responsinle for all types of global product standards, test standards and look into local product regulations in each country globally, including but not limited to the medical devices.
2.Manage to get the medical device CE certificate under 93/42/EEC, ISO 13485 certifiacte, CMDCAS and etc.
3.Responsbile for the medical device registration in each required territory and make sure the product to be launched in each market meet the local regulations.
4.Coordinate with the marketing/design department to make sure the regulations are followed in the product development design and labellings design.
5.Coordinarte with the QS( Quality System) department to make sure the company quality system follows the regulations.
6.Coordinate with the regulation people oversea for some local special registration.
7.Ready to answer all the regulation questions within the company group
8.Other jobs assigned by the supervisor. 举报 分享

苏州翰墨科技有限公司是一家为全球奢侈品牌提供多样服务的优质供应商，2005年成立于苏州工业园区，主要经营生产、加工手握式按摩器、化妆品、服装及其它相关产品。我们旨在为客户提供优质产品及服务，恪守承诺，谋求长远发展，体验前所未有的革新，带领翰墨团队达成客户满意，为员工创造更美好的生活。

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苏州翰墨科技有限公司
地址：江苏省苏州工业园区苏虹中路77号
电话： 86 512 62588561
邮编：215027