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医疗器械注册 10001-20000/月

麦瑞通医疗器械(北京)有限公司

北京

  • 工作年限两年
  • 学历要求本科
  • 招聘人数1
  • 发布日期07-24 发布
  • 语言要求不限
职位信息

职位名称: 医疗器械注册

类别名称:

职位描述:

岗位职责:

Compile and review regulatory submissions, technical files, and labelling for completeness and quality.

 

Identify regulatory requirements for new product and changes to existing products.

 

Determine the scope of information/documentation necessary to file new registration applications and post-approval changes to regulatory agencies.

 

Keep Regulatory Team and appropriate Merit personnel informed of significant regulatory issues affecting Merit products.

 

Provide technical support on specific and/or general issues.

 

Work with operations and customers to resolve and implement corrective and preventive actions resulting from major technical complain

任职要求:

任职要求:

Demonstrate leadership skill and experience in management

Strong analytical skill and ability to execute;

Able to work autonomously;

Good communication skill;

continuous improvement minded

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