Quality Professional

1 week ago


Bengaluru, India Siemens Healthineers Full time

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.

**Organization**: Siemens Healthineers

**Company**: Siemens Healthineers India LLP

**Experience Level**: Mid-level Professional

**Job Type**: Full-time



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