Quality Professional
Bengaluru (Bangalore Urban) IT development
Job description
Evaluate safety complaint escalations, assess and make decisions on medical device reporting (Medical Device Report(MDR)-MedWatch Form 3500A), in accordance with 21 CFR 803, and documenting those decisions.
File MDRs when needed and communicate (as appropriate) to the EU Authorized Representative or Regional Unit.
Refer JD for more details
Organization: Siemens Healthineers
Company: Siemens Healthcare Private Limited
Experience Level: Mid-level Professional
Job Type: Full-time