We've lived the problem. We're building the solution. Come build it with us.
My Audit Corner is growing fast. We're looking for people who want to make a real difference to medical device safety, putting AI at the service of human expertise.
What we build, and why it matters.
Quality and regulatory affairs teams in the medical device industry are drowning in documents, manual checks, and ever-changing requirements. Errors in a technical file can delay a medical device by months, or block it from reaching the market entirely. Behind every dossier, there's a patient waiting.
My Audit Corner is an AI assistant that continuously audits technical documentation (MDR/IVDR) and quality management systems (ISO 13485). We founded it as three field-tested engineers and former quality managers. We had already built, certified, and sold a first Medtech startup (Doc2U, acquired by Biosynex in 2022).
Here, technology serves a clear mission: ensuring every medical device that reaches the European market is safe, compliant, and properly documented.
Here, some of your colleagues will be AI agents.
At My Audit Corner, AI doesn't just live in the product: it shapes the way we work. Part of the team is made up of AI agents. It's our testing ground for understanding, from the inside, what AI really changes for an organization. And the conclusion is counter-intuitive: the more we integrate it, the more central the human becomes.
Radical transparency
When AI agents take part in the work, everything produced becomes visible and traceable. Information flows with no withholding and no blind spots: everyone sees what's being done, and why.
Data decides, the client at the center
We settle things with facts, not opinions or egos. Every decision starts from the same question: what genuinely serves the client?
Even more human
Delegating execution to AI forces us to excel where it can't: kindness, respect, the quality of listening and communication, between us and across teams. It's our number one requirement.
Joining us means learning to work with AI every day. And discovering that it makes us more human, not less.
Why join us?
Joining MAC means being part of a small team where everyone's work is visible, every single week.
Direct impact
Your work has a tangible outcome: better-verified medical devices, better-protected patients. It's not a slogan, it's our daily reality.
AI applied to real problems
No AI for AI's sake. You work on complex domain problems (MDR/IVDR regulation, ISO 13485, advanced RAG) with an immediate, measurable effect.
Accessible founders
Three engineer co-founders, present daily, sharing domain and technical context openly. No politics, no silos.
European market
We address a regulatory market in full transformation (MDR, IVDR, AI Act), with medical device manufacturer clients across Europe.
Open positions
Here are the positions open today. We read every application with care.
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No open position matches your profile? We're always open to spontaneous applications from people driven by our mission.