Role : Postmarket Surveillance Analyst ILocation: Plymouth, MN - 55442Key ResponsibilitiesComplaint Investigation Management: Handle global complaints and adverse events for various products.Perform complaint documentation, coding, and trend analysis.Regulatory Reporting: Independently determine and submit medical device reports to regulatory agencies.Cross-Functional Collaboration: Provide insights to teams such as Regulatory Affairs and Quality Engineering.Must-Have RequirementsEducation: Bachelor's degree required (preferably in healthcare, science, or technical fields).Experience: 1-3 years in complaint handling, medical device reporting, or related areas.Preferred Skills:QA or regulatory experience.Knowledge of global regulations and medical terminology.