Medical Device Surveillance Specialist
11 hours ago
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.
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