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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