Regulatory Affairs
Regulatory Product Surveillance Specialist
Opportunity summary
Employment type: Full time. Requisition: R30209. Start: 2026-09-09. Country: Denmark.
Supporting the safety and clinical compliance of Hearing solutions – Sound like you? In the role of Regulatory Product Surveillance Specialist for the Safety and Clinical Council, within Corporate Quality department, you will contribute to our purpose of Bringing People Closer. You will support post-market surveillance and vigilance activities, while contributing to medical device compliance across relevant areas.
The Team you will be part of:
You will join a team of specialists in Post-Market Surveillance, Vigilance and Usability Engineering within GN Hearing A/S. The team works with complex regulatory matters to help ensure compliant, user-centered products for people with hearing loss. We are a collaborative and quality-focused team that values continuous learning, curiosity and respectful dialogue.
We welcome diverse perspectives and work closely together to find sound, practical solutions. Your contribution is appreciated, and you will:
- Manage safety-related customer feedback - MDR/Vigilance reporting within applicable regulatory framework - Ensure regulatory compliance 1 …
This is a shortened extract from the public vacancy. Follow the original posting for the complete and authoritative description.