Protege (Quality)
Siemens Lihat semua pekerjaan
- Kuala Lumpur
- Tetap
- Sepenuh masa
- You will be responsible to support the preparation of CSDT for submissions with MDA, MoH.
- You will be responsible to support the adverse event reporting with MDA, MoH.
- You will be responsible to support all general administrative task within Quality department.
- Support to consolidate & prepare change notification submissions with MDA, MoH.
- Basic knowledge in product registration for medical devices based on the requirements from Medical Device Authority, MoH.
- Basic knowledge in product change notification submission for medical devices based on the requirements from Medical Device Authority, MoH.
- Basic knowledge in adverse event reporting for medical devices based on the requirements from Medical Device Authority, MoH.
- University degree in natural sciences (for example biomedical, pharmaceutical studies or medical engineering) or equivalent.