长沙招聘

感兴趣可把简历发到karen.kong@db-talent.cn的邮箱，或者加V.X: Karen_DB 详聊

主要做合规管控 support 美国

医疗器材/制药行业都可以 （must）

英文好 （must)

团队管理经验（must)

base 上海or 武汉都可以， 但必须要base office 的

team 6人，上海，武汉 + 越南*2

不用做注册的， 他们有市场团队做注册， 主要做合规， 但不用做的很专，以前做过的就可以

1. Responsibility

1.1 Primary Responsibility

1) Build team goals of Medline China RA team, work for related sources and methods, monitor the progress and keep to the success;

2) Work on shared Medline quality goals and keep to the success;

3) Develop, organize and implement clear team development plans with comprehensive consideration of Medline needs and resources;

4) Develop and organize continuous improvement projects of Medline Asia RA team;

5) Provide regular assessments, suggestions and guidance for supervisors on personnel and project managements;

6) Help on projects and problems related to RA team which need cross-functional cooperation and work on mutual solutions when there are conflicts;

7) Support and make guidance on challenging projects/problems in Medline Asia RA team;

8) Organize or make training for new hires, co-workers and suppliers on regulatory affairs and processes related to Medline Asia RA team.

1.2 Secondary Responsibility

1) Support on overall Medline quality improvement projects

2) Backup for related supervisors or manager when necessary;

3) Others assigned by manager

2. Requirements

2.1 Education and skills

1) Bachelor degree at least, science background is preferred;

2) Fluent both in written and verbal English, CET 6 or equivalent or above;

3) Familiar with general office software, especially excel and PPT;

4) Know about common registration, certification and licensing regulations about medical devices in EU, US and China;

5) 5 years’ work experience in RA field and 3 years in management at least;

6) Good at managing multiple projects at the same time;

7) Able to work under pressure;

8) Good at planning and organizing;

9) Good self-learning sk

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