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Medical Device Surveillance Specialist

1 month ago

Burlington, Vermont, United States KYYBA Full time
Job Summary

Seeking a highly skilled Medical Device Surveillance Specialist to join our team at Kyyba. As a key member of our post-market surveillance department, you will be responsible for reviewing and classifying adverse events and medically related complaints for on-market products.

Key Responsibilities:

  • Determine classification, review, and disposition of adverse events and medically related complaints
  • Complete FDA MDR and other outside competent authority regulatory reports
  • Collaborate with cross-functional teams to ensure compliance with regulatory requirements

Requirements:

  • 0-2 years of experience in post-market surveillance or a related field
  • Four-year degree in a healthcare or science field, or 2-year degree with relevant experience
  • Strong analytical and problem-solving skills

About Kyyba:

Kyyba is a global leader in delivering high-quality resources and top-notch recruiting services. Our company culture embodies our core values of value, passion, excellence, empowerment, and happiness, creating a vibrant and productive atmosphere. We empower our employees with the resources, incentives, and flexibility they need to support a healthy, balanced, and fulfilling career.