职 位 描 述: |
职位描述:
Job Description:
- 负责及时与客户联系、沟通,了解客户所在国家的法规注册要求;
- Be responsible for contacting and communicating with international customers in time to catch up with all requirements from these customers and related counties.
- 负责按照除美国外各国法规要求,准备产品的注册资料;
- Prepare material for product register according to Government laws and regulations, excepting FDA.
- 产品注册资料报送国家食品药品监督管理部门;
- File and send the register material to Food and Drug Administration.
- 负责相关政府部门及检测机构的联系、沟通;
- Be responsible for contacting to and communication with the related government departments and inspection institute.
- 在需要时,向公司管理部门提供相关的法律法规信息和建议;
Provide the information of related law or regulation and advice to company’s management when needed.
- 帮助工厂准备质量体系的现场考核;
Assist plant to prepare the field evaluation of quality system.
工作胜任要求:
Job Requirements:
- 本科以上学历或相关专业大三学生;
- Bachelor degree or above;
- 熟悉中国医疗器械法律法规;
Familiar with international pharmaceutical device law and regulation;
- 熟悉三类医疗器械注册流程;
- Familiar with register process;
- 工作积极主动,能够承受工作压力;
- Initiative working attitude, be able to work under pressure.
- 良好的英语口头及书面沟通能力;
- Good oral and writing communication skills in English;
- 具有良好的团队合作精神.
- Good team-work spirit.
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