Associate Regulatory Specialist 助理合规专员
麦朗(上海)医疗器材贸易有限公司
- 公司规模:150-500人
- 公司性质:外资(欧美)
- 公司行业:医疗/护理/卫生
职位信息
- 发布日期:2020-09-07
- 工作地点:武汉-武昌区
- 招聘人数:1人
- 工作经验:2年经验
- 学历要求:本科
- 职位类别:质量管理/测试工程师(QA/QC工程师) 医疗器械注册
职位描述
JOB RESPONSIBILITIES
1.Review and approve product labeling using information provided by product managers, vendors, divisional QA's and marketing.
2.Review and approve promotional literature in paper or electronic format using information provided by product managers, vendors, divisional QA's, sales and marketing.
3.Communicate requirements of regulations as needed to internal or external customers, or to vendors, and formally train others on department procedures as required
4.Maintain department databases and files as required
5.Initiate or maintain relevant procedures or SOP's, updating as needed and training when required
JOB REQUIREMENTS:
1.College degree required, or equivalent work experience in quality or regulatory affairs
2.Detail oriented, with excellent organizational skills and above average spelling/grammar abiities and proficiency in Word, Excel, and SAP
3.Must be able to communicate effectively in both written and oral modes in English, and to work independently and within a team
4.Must be able to learn quickly, to assimilate and retain large quantities of new information effectively, and to enjoy research and investigation into issues and for problem-solving
公司介绍
Our Website: https://medlineasia.com.cn/
联系方式
- Email:hrchina@medline.com
- 公司地址:建设大道588号卓尔国际中心