Surveillance Analyst

2 weeks ago


St Paul, United States Intellectt Inc Full time

Role: Product Surveillance Analyst (Medical Device/Pharma)

Location: St. Paul, MN 55117 (Plymouth or St. Paul location)

Duration: 11 Months (Contract to hire) on W2

Shift: 7 AM to 4 PM or 9 AM to 6 PM


# Local candidates

# On-Site and travel between Plymouth and St. Paul.


Job Requirements:

  • Experience: 0-2 years; postmarket surveillance in Medical Device or Pharmaceutical Industry preferred.
  • Education: 4-year degree in healthcare/science fields (Bio, Chem, Life Sciences), or 2-year degree with relevant complaint handling or investigation experience.
  • Skills: Complaint handling, FDA MDR reporting, product investigation, cross-functional communication, highly organized, lab experience preferred.

Responsibilities:

  • Classify, review, and resolve adverse events or medical complaints for on-market products.
  • Determine seriousness, reportability, and causality of complaints.
  • Complete regulatory reports (FDA MDR, others).
  • Analyze and submit product complaints or investigate returned surgical products (some biohazard).


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