---
bio: 'I have worked in the medical device industry for approximately five years, gaining
  experience in both large MedTech organizations and startup environments. Throughout
  my career, I have contributed to the development of FDA-regulated medical devices
  across the full product lifecycle, including software development, AI and machine
  learning applications, regulatory strategy, verification and validation, risk management,
  and 510(k) submissions.\

  Over the course of my career, I have worked on products at various stages of development,
  from early concepts to regulatory submission. This experience has given me an appreciation
  for the balance between technical innovation, product quality, and regulatory compliance.\

  One of the biggest lessons I\''ve learned is that successful medical device development
  is a team effort. Whether working with engineers, clinicians, quality, or regulatory
  professionals, clear communication and collaboration are critical to getting products
  to market. I enjoy working with cross-functional teams to solve problems and deliver
  products that can make a real impact on patient care.'
hire_date: '2026-06-15'
hobbies: ''
linkedin: https://www.linkedin.com/in/michael-millan
name: Michael Millan
photo: /img/people/Michael_Millan-37cbd5b7a754801abd4ce0791937c2b0.jpg
skills: SaMD Development, AI/ML, FDA Strategy, Cybersecurity, Algorithms
testimonials: []
title: Senior Software Engineer I
---