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| 搜索工作首页 > 通用电气(中国)有限公司(医疗集团--GEChina-Healthcare) > 医疗器械注册专员RegulatoryAffairsSpecialist |
医疗器械注册专员RegulatoryAffairsSpecialist |
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| 医疗器械注册专员RegulatoryAffairsSpecialist职位说明及要求 | |
Description: Work with the Global SREs to develop and apply Chinese pre-market approval. Including SFDA, CCC, SBTS, etc Certification. Work with marketing and sales to support regulatory affair activities. Manage Chinese GB, YY, JJG, SJ standards and delivery to P&L to adopt timely. Monitor the Chinese regulation implementation. Qualifications: 1.Bachelors Degree or equivalent, Preferable in electrical or mechanical degree. 2.Minimum 3 years experience working in Regulatory Affairs 3.Strong interpersonal skills, ambitious and aggressive personality, can work under pressure. 4.Excellent English communication skills in both spoken and written. 5.Very accountable and detailed working attitude. 6.Be proactive thinking. 7.Analytical & problem solving skills. 8.Results Orientation, Ability to Learn. 9.Basic product knowledge awareness is preferred. |
| 通用电气(中国)有限公司(医疗集团--GEChina-Healthcare)地址和其它联系方式 | |
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电子邮箱:weiqi.luan@ge.com 公司网址: |