Regulatory Affairs Specialist

iO Associates - UK / EU; Berlin; Remote; EUR 55.000 - 75.000; Vollzeit

Zusammenfassung

Join a leading digital health platform as a Regulatory Affairs Specialist, overseeing compliance for Software-as-a-Medical-Device. Collaborate with development teams to translate regulatory requirements and make a significant impact on the business's regulatory processes. Enjoy a remote-friendly setup with travel to Berlin every two months, supported by the company.

Leistungen

Remote friendly setup

Paid travel and accommodation to Berlin

Qualifikationen

• Hands-on experience with ISO 13485 for Software-as-a-Medical-Device.
• Worked on Software-as-a-Medical-Device (SaMD) with regulatory challenges.
• Can write technical tickets for developers based on compliance or quality requirements.

Aufgaben

• Oversee compliance and regulatory processes in digital health.
• Translate regulatory requirements into actionable Jira tickets.
• Support audits and manage technical documentation.

Kenntnisse

Fluent in German

Fluent in English

Regulatory knowledge

ISO 13485

GDPR

Documentation skills

Tools

Jira

Confluence

Jobbeschreibung

Regulatory Affairs Specialist | Digital Health | Berlin (Remote)

iO Associates are partnering with a leading digital health platform, in their search for a Regulatory Affairs Specialist. This is a newly created role due to good company growth where you will be overseeing compliance and regulatory processes within their digital health business.

Being part of the Product team, you will be collaborating with developers and project managers and translating regulatory requirements into actionable Jira tickets. Your responsibilities include supporting audits, managing technical documentation, and ensuring compliance with related standards, making you a pivotal figure in the business's regulatory efforts.

Experience required :

• Hands-on experience with ISO 13485 for Software-as-a-Medical-Device in a software company.
• Have worked on Software-as-a-Medical-Device (SaMD) and understand its regulatory challenges.
• Can write technical tickets for developers based on compliance or quality requirements.
• Are fluent in German and English (C1+)
• Experience with GDPR, ISO 27001, IEC 62304, or similar regulations.
• Familiarity with Jira, Confluence, or other documentation / ticketing tools

This is an exciting time to join a growing medically certified digital health app business - you will be able to shape the regulatory foundation, work with cutting-edge technology and a fast-growing, mission-driven team. So, if you're passionate about compliance, digital health, and bridging the gap between regulation and implementation, please apply now!

Please note that you will be required to travel to Berlin every two months - travel and accommodation will be paid by the company, and they do provide a remote friendly set-up. And you must have the right to work in Germany - sponsorship is not provided.