**In this role, you will have the opportunity to**
Support MR system verification activities and reliability activities during medical product development. Communicate with design team, global team and other function team to deliver a high-quality product.
**You are responsible for**
+ Lead NMPA registration for standard compliance
+ MR subsystem & system integration test.
+ MR subsystem & system safety, image quality, reliability test.
+ Support impact analysis on feature/design changes
+ Release documents for medical device registration
**You are a part of**
A progressive and energetic team that contributes directly to the growth of the business.
**To succeed in this role, you should have the following skills and** **experience.**
+ Bachelor or higher degree in physics, biomedical engineering, Electrical _& E_ lectronic _Engineering_ , greater than 10-15 years working experience.
+ Good English communication skill with cross function team
+ Expe...