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Analyst, Product Surveillance

In Minnesota / United States

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Analyst, Product Surveillance   

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JOB TITLE:

Analyst, Product Surveillance

JOB TYPE:

JOB SKILLS:

JOB LOCATION:

St. Paul Minnesota / United States

JOB DESCRIPTION:

Exempt/Non Exempt: Non ExemptYears Experience: 0 - 2 yearsSkills: Related experience in post market surveillance in a Medical Device or Pharmaceutical Industry preferred. Education: Four-year degree, preferably in the healthcare or science fields; or 2-year degree and relevant experience supporting complaint handling investigations, medical device reporting, or product analysis. Degreed applicants without medical, scientific, or complaint handling experience may be considered if they possess the strengths suitable for this position. Duties: May perform multiple functions within the postmarket surveillance department. 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. Complete FDA MDR and other outside competent authority regulatory reports.

Position Details

POSTED:

Sep 10, 2022

EMPLOYMENT:

INDUSTRY:

SNAPRECRUIT ID:

S1657220408147132

LOCATION:

Minnesota / United States

CITY:

St. Paul

Job Origin:

Jobsrus_organic_feed

A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
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Exempt/Non Exempt: Non ExemptYears Experience: 0 - 2 yearsSkills: Related experience in post market surveillance in a Medical Device or Pharmaceutical Industry preferred. Education: Four-year degree, preferably in the healthcare or science fields; or 2-year degree and relevant experience supporting complaint handling investigations, medical device reporting, or product analysis. Degreed applicants without medical, scientific, or complaint handling experience may be considered if they possess the strengths suitable for this position. Duties: May perform multiple functions within the postmarket surveillance department. 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. Complete FDA MDR and other outside competent authority regulatory reports.


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