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Posted:3 weeks ago| Platform: 
Work from Office
Full Time
Proficient in preparing & submitting regulatory fillings for product approvals, conducting clinical evaluations, managing risk assessments, ensuring post market compliance. Experienced in EU MDR 2017/745, US FDA, Indian MDR 2017 & ISO 13485 Standards Required Candidate profile Candidate from Medical Device company will be preferred. Deeply knowledge of EU MDR 2017/745, CE Marking, US FDA, Indian MDR 2017, ISO 14971 and Risk Management is mandatory for this position.
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