Analyst, Product Surveillance II
o May perform multiple functions within the post market surveillance department.
o Major responsibilities would include determining classification, review, and disposition of adverse events and medically related complaints for on-market products, including decisions on seriousness, reportability, and potential causality.
o Complete FDA MDR and other outside competent authority regulatory reports.
o Managing product experiences determining classification, disposition of adverse events, complaints for post market products, sending FDA medical reports to Regulatory locations (Europe and Hong Kong), etc.
Recommended Skills Project Management Analysis Benchmarking (Project Management) Timelines Process Design Metrics Estimated Salary: $20 to $28 per hour based on qualifications.
o Major responsibilities would include determining classification, review, and disposition of adverse events and medically related complaints for on-market products, including decisions on seriousness, reportability, and potential causality.
o Complete FDA MDR and other outside competent authority regulatory reports.
o Managing product experiences determining classification, disposition of adverse events, complaints for post market products, sending FDA medical reports to Regulatory locations (Europe and Hong Kong), etc.
Recommended Skills Project Management Analysis Benchmarking (Project Management) Timelines Process Design Metrics Estimated Salary: $20 to $28 per hour based on qualifications.
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