Regulatory Affairs Leader, XR 3267244
GE医疗集团
- 公司规模:5000-10000人
- 公司行业:医疗设备/器械
职位信息
- 发布日期:2019-04-06
- 工作地点:北京
- 招聘人数:若干人
- 工作经验:无工作经验
- 学历要求:招若干人
- 语言要求:不限
- 职位类别:法务主管/专员
职位描述
Role Summary/Purpose :This position provides subject matter guidance. He/she works within a team of Regulatory Affairs professionals to ensure GEHC establishes best practices in compliance with regulatory requirements. The Regulatory Affairs Leader will be involved with regulatory activities in the areas such as premarket submissions, post-market reporting, regulatory intelligence, regulatory requirements flow-down advertising and promotion review, product labeling compliance, etc.
Essential Responsibilities :1. Provides regulatory input for product development to ensure compliance to regulatory requirements for target markets 2. Develops regulatory strategies to help guide regulatory submission pathways, taking into consideration regulatory requirements (including product testing, clinical data, etc), product claims and country regulatory dependencies to ensure optimized sequencing for submissions, 3. Works with a cross functional team to prepare and submit regulatory submissions to regulatory authorities for the purpose of obtaining authorization for market launch. 4. Assesses changes in existing products to and determines the need for new / revised licenses or registrations. 5. Develops plan for timely submission of renewal registrations for applicable countries per business plan, to ensure continued product supply in those countries. 6. Reviews and approves advertising and promotion material to ensure consistency with approved claims and regulatory requirements. 7. Contributes to writing and editing technical documents 8. Researches, analyzes, integrates and organizes background information from diverse sources for regulatory submissions 9. Understands and applies regulatory requirements and their impacts for submissions 11. Ensures compliance with pre- and post-market product approval requirements 10. Supports regulatory inspections as required. 11. Assesses adverse events and field actions for reportability to regulatory authorities and prepares and submits reportable events and recalls in a timely manner to regulatory authorities, as per country regulations. 12. Performs a broad variety of tasks in support of product and process design as assigned by the departmental manager
职能类别: 法务主管/专员
公司介绍
联系方式
- Email:Lei.zhu@ge.com