Position Details:

Client: Medical Device

Job Title: Analyst, Product Surveillance

Duration: 12 months [++ Possibilities of extension]

Location: Plymouth, MN 55442

Responsibilities:

•  Experience: 0 - 2 years
• 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.