东莞招聘

職責笵圍(請詳細列明):
1. work with product development team to perform product.
clinical evalualation for new product.
2. develpment and update the clinical information
for marketed product.
3. Perform post market clinical follow-up studies for
marketed products.
4. Update post production information for marketed products.
5. Update Regulatory and standards (FDA, Health Canada, EU) information every month.
6. Have leadership skill to lead the team to finish the product resgistration in CE
要求資格:
性別: 不限 年齡: 25-45
學歷:qualification: Bachelor or advanced degree in clinical,
medicine, pharmacy, biomedical, or related discipline
相關經驗年資; at least 5 yrs experience in regulatory affairs
技能:Skills
1.rich experience in clinical study are preferred.
2. successful experience with clinical evaluation for CE registration.
3. Good ability to search literatures from the databases of EU or other countries.
4. Demonstrated in the active medical device regulatory standards and skillful in the standards with respect to the electrosurgical insturments.

欢迎您加入PSC公司，并将PSC作为您的事业！
深信您的到来会给我们的企业注入新的活力，让我们的思维更加敏捷、视野更加开阔，使我们的生活更加充实、未来更加美好！
PSC公司隶属于（HK）Modern Medical Corporation (MMC)集团公司，集团公司集研发、生产、经营于一体，致力于发展创新、追求卓越品质的医疗器械之事业，并奉行为社会服务，为人类奉献之原则！
PSC公司成立于一九九七年，公司致力于精良先进、科技前端的医疗器械的销售事业，祈望带给世界绿色生命、祝福人类幸福美满！

公司文化倡导：
广纳诚信、高效、精英之员工；
为全球创造和谐健康人类生活奉献卓越、优质之产品！

公司福利：
1、五险一金（综合医疗）
2、五天八小时工作制
3、劳动法规定的带薪年假
4、员工生日会
5、定期旅游（根据公司运营状况）
6、和谐的企业文化