Title: Product Surveillance Analyst-Medical devices

Location: St. Paul, MN (may also require travel to Plymouth, MN)
Duration: 11 Months

Job Description

Experience Required:
0 - 2 years in a relevant field

Preferred Skills:

• Experience in post-market surveillance within the Medical Device or Pharmaceutical industry
• Strong organizational skills and ability to prioritize tasks
• Excellent cross-functional communication skillsEducation:
• Four-year degree in healthcare or science fields (e.g., biology, chemistry, life sciences)
• Alternatively, a two-year degree with relevant experience in complaint handling investigations, medical device reporting, or product analysis may be considered.
• Key Responsibilities:
• Determine classification, review, and disposition of adverse events and medically related complaints for on-market products
• Assess seriousness, reportability, and potential causality of complaints
• Complete FDA MDR and other regulatory reports
• Analyze and submit complaints, and investigate returned products from the field (some may be biohazard)

Additional Information:

• The role is contract to hire and requires 100% onsite presence.
• Candidates must be local to Minnesota and able to work at both Plymouth and St. Paul locations as needed.
• Experience in complaint handling and product performance investigation is a plus.

If you are interested and willing to apply! Please contact me at or +1-732-653-9472