Quality Assurance, Post Market Specialist

What you’d do

Perform post-market surveillance to ensure regulatory compliance, review product complaints and adverse events, interact with customers for information, and support risk assessments and quality investigations in a medical device context. Full-time position. Found on the employer's careers page on Oct 21, 2026. Apply through the link.

You’ll need

• 1 year post-market surveillance or related experience
• Experience in medical device industry
• Exposure to medical device product development
• Clinical or nursing experience
• ECG rhythm interpretation skills