Fast and efficient registration for responsible products and contribute the time to market.
Areas of Responsibilities:
1. Work together with BL RA for all registration activities include testing, documents preparation, submission and achieve product license target in fast and effective way.
2. Maintain or develop good working relationship and cooperation with relevant authorities like test labs, CMDE etc. to improve working efficiency;
3. Provide regulatory support on both pre-market and post-market issues on responsible product lines;
4. Coordinate and lobby in new regulation and standards related to medical device registration.
- Bachelor’s degree or above relevant in medical/ biological/engineering etc.
- Above 3 years in regulatory affaires
- Good experience in medical device product registration
- Working experience in MNC
Organization: Siemens Healthineers
Company: Siemens Healthineers Ltd.
Experience Level: Experienced Professional
Job Type: Full-time