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Analyst, Product Surveillance

Experis
Plymouth, MN
  • Healthcare
  • Contract
  • product surveillance
  • postmarket surveillance
  • medical device reporting

Our job summary

The Analyst, Product Surveillance is responsible for postmarket surveillance activities including classification, review, and disposition of adverse events and medical complaints related to on-market products. The role involves completing FDA Medical Device Reports (MDR) and other regulatory submissions, managing complaints via specialized systems, and supporting complaint handling investigations. Candidates typically have a healthcare or science background and 0-2 years of relevant experience in medical device or pharmaceutical industries.


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