We’re excited to welcome Jorrit Boersen to the MedQAIR team as our newest Consultant. With a strong background in Technical Medicine and a focus on regulatory strategy for medical device software and AI, Jorrit brings a thoughtful, pragmatic approach to global market access. His experience spans EU-MDR, global submissions, and cross-functional collaboration across EMEA, North America, and APAC.
Curious by nature and driven by impact, Jorrit is passionate about helping bring safe, innovative technologies to patients faster. We sat down with him to learn more about his journey, his thoughts on the future of AI in healthcare, and what excites him about joining MedQAIR.
Learn more about his journey, motivations, and vision for the future of AI in healthcare.
1. Can you briefly introduce yourself and your professional journey so far?
I began my career in clinical research, which gave me valuable insight into clinical environments and patient care, something that still shapes my work today. I gradually transitioned into the medical device industry, where I worked with companies of various sizes, from startups to large enterprises, and across a broad range of devices and therapeutic areas.
Over time, I specialized in regulatory affairs, with a particular focus on medical software and artificial intelligence. Most of my work has centered around EU medical device regulations, but I’ve also supported global registration efforts in markets across APAC, North America, and EMEA. My experience spans both in-house roles, including as a regulatory affairs specialist at a software company, and consulting roles where I’ve helped clients navigate complex regulatory landscapes.
2. What inspired you to work in the medical device industry?
The chance to work with new technologies while improving healthcare outcomes really drew me in. That combination still motivates me today.
3. What drew you to MedQAIR, and what are you most excited about in this new role?
MedQAIR aligns with my personal drive to help. I’m excited to contribute to better healthcare through software and innovation, and to work with a team that shares this mission.
4. Can you tell us about your background in software and how it intersects with your work in healthcare?
I’ve worked as a regulatory affairs specialist at a software company for several years, collaborating closely with software developers. Before that, I gained hands-on experience using various software tools in a hospital setting. This dual perspective—from both the development and user side—helps me understand how to bridge the gap between tech and clinical needs.
5. How have you seen software transform the medical field in recent years?
Like in many other fields, software has driven digitization in healthcare, and more recently, advanced AI tools are helping support both healthcare professionals and patients in meaningful ways.
6. Any favorite projects you've worked on that involved software or digital health solutions?
I’ve been fortunate to work on several projects involving digital health and software, where I got to collaborate with great people and explore innovative technologies. Those are always the most rewarding experiences.
7. How do you see artificial intelligence currently impacting the medical device industry?
AI is transforming the medical device industry by streamlining access to critical information and supporting tasks like diagnostics, data analysis, and workflow automation. This should enhance decision-making and efficiency, allowing teams to focus more on high-value, patient-centered work.
8. What are the biggest challenges companies face when integrating AI into healthcare products or processes?
One of the biggest challenges is getting reliable, high-quality data to train and validate AI systems. Without trustworthy information, it’s difficult to build tools that are accurate, safe, and clinically useful
9. In your view, where is AI most underutilized in the healthcare space today?
From my experience, image analysis was an area where AI was underutilized for too long. It had the potential to reduce workload and boost efficiency – something we’re now seeing more progress in.
10. Where do you think AI will make the most difference in the next 5–10 years in healthcare?
In the next 5-10 years, I believe AI will make the biggest impact by improving both the speed and accuracy of diagnostics, treatment planning, and administrative workflows
11. What do you think companies can do better when it comes to using AI responsibly and effectively?
Transparency is key. Companies can improve the responsible and effective use of AI by being transparent with users about AI, what data they use, and how decisions are made. Clear communication builds trust, helps users understand the technology, and ensures ethical use while encouraging accountability.
12. How do you balance innovation with patient safety and regulatory requirements?
By taking a pragmatic approach to regulatory requirements, applying the requirements efficiently while keeping patient safety as the top priority. That way, innovation can move forward responsibly.
13. What are some opportunities for MedQAIR to lead in this space?
MedQAIR has a great opportunity to lead the way in using software and AI to streamline regulatory processes, helping bring safe and effective medical technologies to patients faster.
14. What values do you look for in a team or organization you work with?
Openness, curiosity, and teamwork. These values create the best environment for solving tough problems together.
15. Outside of work, what keeps you inspired or motivated in your field?
I stay inspired by staying connected with people. Conversations and shared ideas make me feel excited. Also, having something ahead to plan for, even just the next run or challenge, keeps me motivated.
Welcome to the team, Jorrit! We’re thrilled to have you on board and look forward to the impact you’ll make with MedQAIR.
Interested in streamlining your regulatory process? Get in touch with MedQAIR to see how we can support your team.
