Job Description

Recent Biomedical Engineer, 100% onsite in Minnetonka, MN

Job Description:

• Drive the safety and quality of our on-market medical devices


• You'll classify, review, and determine the disposition of adverse events and medical complaints, including seriousness, reportability, and potential causality.


• Key responsibilities include completing FDA MDR and other regulatory reports.

Required:

• Four-year degree (healthcare/science preferred)


• Relevant experience in complaint handling, MDR, or product analysis.


• Strong analytical and problem-solving skills are essential.

Preferred:

• Experience in post-market surveillance within the medical device or pharmaceutical industry.

Pay range:

$25/hr. - $28/hr. 

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