Regulatory Education Specialist (Quality)

We pull medical technology from the future to solve human health.

Authorised by governments around the world to assess medical AI, we remove unnecessary delays from every regulatory approval we do so patients get devices from the future, today. We are proud to count the world’s most ambitious companies building medical technology as customers. You will be joining a team with product-market fit, flowing data, and exponentially growing revenue.

Who you are:

• You have 3+ years of experience supporting Quality Management System (QMS) implementation, audit preparation, or regulatory compliance activities under EU MDR, UK MDR, MDSAP, and/or ISO 13485.

• You understand what makes a high-quality QMS and what it takes to prepare companies for audits.

• You have experience teaching, designing training, or working with Learning Management Systems.

• You’re motivated by the opportunity to shape how high-quality regulatory and quality documentation is taught, learned, and standardised at scale.

• Your verbal and written communication skills are exemplary, aligned with MECE principles and adapted to an asynchronous work environment.

What the job involves:

• Create high-quality content that enables medical device innovators to understand the QMS and audit requirements of EU MDR, UK MDR, MDSAP, 510(k), ISO 13485 and others.

• Design education-grade materials, including slides, diagrams, lesson plans, and voiceover scripts, for use across videos, knowledge base articles, and enablement tools.

• Lead structured dialogues that clarify core concepts, surface common pitfalls, and align medical device innovators on what “good” looks like.

• Work closely with the auditors to ensure that everything we publish reflects a consistent, aligned regulatory view.

The Interview Process

• Intro call with

• Round 1: Team interviews: Interview with Steven and Johan (2x30 min)

• Round 2: Founder interviews: Interview with and (2x30 min)

• Referencing

• Offer