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Open nowPosted 223 days ago

技术法规工程师

syounggroup/career145 open roles

Where
Changsha, Hunan, Chinese Mainland
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Your applicationOpen now技术法规工程师syounggroup/career · Changsha, Hunan, Chinese Mainland
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The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market. syounggroup/career postings stay open a median of 1 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.3%14 days
  5. 35.6%30 days
  6. 57.8%60 days
This job: posted 223 days ago

syounggroup/career median: 1 days open

The posting

1. 负责根据公司产品海外销售布局(重点欧盟、美国),精准确认化妆品检验项目、检验周期,统筹产品送检全流程,负责检验报告的整理、审核、归档,确保检验环节合规可追溯,适配海外市场准入要求。 2. 负责产品全链路合规审核,重点对产品标签标识、说明书、宣传进行全面合规把控; 3. 负责化妆品配方合规审核,结合欧盟、美国原料管控规范(如欧盟REACH法规、美国FDA原料要求),核查配方合规性并提出优化建议; 4. 负责化妆品在欧盟、美国的登记备案全流程工作,包括但不限于欧盟CPSR、PIF资料的编制、审核、提交,欧盟CPNP通报、美国FDA Product List登记,确保备案/登记高效落地、按时完成。 5. 负责欧盟、美国化妆品相关法规、政策的动态追踪、收集与更新,建立法规动态台账,及时同步至研发、业务等相关部门,开展法规宣贯与指导; 6. 配合公司海外业务拓展,提供合规技术支持,解答各部门海外法规相关疑问,协助处理海外合规突发问题;

1、本科及以上学历、化学,药学相关专业,具备3年以上欧盟和美国化妆品的法规工作经验; 2、中英文为工作语言,具备流利的中英文读写、沟通能力,熟悉海外文化,有海外留学、海外合规工作经验者优先; 3、精通欧盟(EC 1223/2009法规、CPNP通报、CPSR/PIF编制规范)、美国(FDA化妆品法规、Product List登记要求)化妆品相关法规、政策及行业标准,能独立完成备案资料编制、合规审核、法规解读工作。 4、办公软件操作技能:能熟练操作日常办公软件(Xmind、Excel、PPT、Word),借助办公软件能快速进行数据处理,SOP编写,操作表格制定,PPT方案。 5、综合素质:具备严谨细致的工作态度、较强的责任心和执行力,具备良好的跨部门沟通协调能力和抗压能力,能独立处理合规相关事务,应对海外合规突发情况。

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