北京招聘

Main Responsibilities:

1.Interface with China RA team and Global Supply Chain to review Chinese DFU & labeling content and control the quality;
2.Handle customer complaint / product quality issue/ Medical Device Adverse Event reporting, work with sourcing companies on product quality complaints in China.
3.Ensure Supply Chain activity and cycle to be aligned with Regulatory Affairs information, meanwhile, in accordance with the company SOPs and local regulations;
4.Control documentation that complies with SFDA regulations and relevant requirements in China;
5.Provide active and strong regulatory supports to internal departments for post market surveillance;
6.Support supply chain program implementation in China;
7.Keep all records and filings well and clear.

Minimum Position Requirements:

1.Academic/Professional Education, Medicine & Clinical bachelor or above;
2.Proficiency in English;
3.At least three years experiences on regulatory compliance or quality assurance, familiarity with ISO9000, ISO 13485, SFDA & China relevant regulation;
4.Good communization skill and getting along with people on the same page.

爱尔康成立于1945年，目前总部位于瑞士日内瓦。作为眼健康领域的引领者，自成立以来一直专注于视力健康，致力于为全球140多个国家和地区的人们带来更好的视觉体验。
爱尔康于1995年成立中国公司，致力于为国内眼科专家、患者和消费者提供更好的解决方案。爱尔康中国不仅提供创新的产品和服务，还竭诚为国内眼科医生打造国际化的学习交流平台，积极推动中国眼科事业的发展。此外，企业还同眼科基金会等慈善机构紧密合作，支持各类扶贫项目，为中国的防盲治盲工作贡献力量！
2019年4月，爱尔康在瑞士证券交易所和纽约证券交易所同步上市。企业持续秉承对客户、患者和消费者的承诺，通过引领眼科及视力保健产品的突破性创新改善视觉质量，提升人们的生活品质，与大家一道共见精彩！