Security is not a barrier to innovation. It is what makes innovation trustworthy.
About Me
We live in a fast-moving, technology-driven world. As innovations like AI and machine learning move deeper into healthcare, the stakes around cyber risk have risen sharply. Connected medical devices and digital health products now carry real consequences for safety, trust, and resilience. Compliance alone is no longer enough. Resilience is what keeps products, and the people who rely on them, actually protected.
That conviction is what shapes my work and my journey.
My Journey
I am a cybersecurity professional working with product and engineering teams to build secure, privacy-conscious digital health products for regulated environments. My work connects product security, cyber risk, privacy, compliance, and product resilience across the total product lifecycle, with a focus on building trust as a MedTech Cybersecurity Advisor.
Over the past 12+ years, I have worked across sales, finance, IT operations, and information security. That path shaped how I approach cybersecurity today, not only as a technical discipline, but as a driver of business resilience, product trust, and risk-informed decision-making.
My academic background reflects the same breadth. A Bachelor of Education from the University of Ibadan, an MBA in International Business and an MSc in Investment and Risk Finance from the UK, and an MSc in IT Security Management in Berlin. Each qualification added a layer of perspective that purely technical training alone would not have provided.
Across organizations including EY, one of the Big Four professional services firms, ALDI International Services, and ZEISS Medical Technology, I have built experience spanning consulting, information security, cyber risk, and product security, working with teams and clients across Europe, the US, and beyond.
Today, at ZEISS Medical Technology, I work with product and engineering teams to embed security and privacy into digital health products from the ground up. That includes threat modeling, vulnerability management, cloud security, and AI security, guiding teams through FDA premarket submissions such as 510(k) and eSTAR cybersecurity documentation, and through EU MDR technical documentation for Notified Body conformity. I also contribute to internal working groups shaping how my organization approaches vulnerability management, technical risk assessment, and the security of AI-enabled products, in line with frameworks like the EU AI Act, the NIST AI Risk Management Framework, and OWASP AISVS. The goal is never compliance on paper. It's products that hold up under real conditions.
Through Regulated Cyber, a free publication I write as Editor-in-Chief, I share that thinking more widely. I cover MedTech cybersecurity and privacy, AI security in regulated products, data protection, and product security career growth, aiming to make complex regulatory and technical topics clear by connecting public guidance, industry practice, and real product security experience.
If you would like to connect or follow the work, I am most active in two places.
Read Regulated Cyber