We are helping a leading digital health company that is empowering over 30 million users worldwide to enhance their cognitive abilities and maintain independence in daily life.
Working closely with developers and project managers, you will translate complex regulations into clear, actionable Jira tickets and ensure they are executed and documented in compliance with our quality standards.
This is an ideal opportunity for someone who thrives in a dynamic tech environment while bringing strong regulatory knowledge and hands-on experience in Software-as-a-Medical-Device (SaMD).
Translate compliance requirements into actionable developer tickets (e.g., Drive awareness and implementation of compliance practices across the organization
Solid experience applying ISO 13485 in a software-focused (not just hardware) medical device company
German speaking ( C1 level )
Direct involvement with Software-as-a-Medical-Device (SaMD)