This week’s Relay Interview features Shinjae Park, our RA specialist. “RA” stands for Regulatory Affairs, referring to experts who ensure that medical devices meet legal and regulatory standards across different countries. Shinjae played a key role in our recent ISO 13485 recertification audit, and today we’re sharing their journey of adapting to life at Promedius.

Q. You’re now three months into your role. What’s a typical day at Promedius like?

A. I’m still in the process of adjusting. In the medical device field, quality management systems are critical because they demonstrate a product’s safety and reliability. The recent ISO 13485 audit was the first one I participated in since joining, and I felt both pressure and a strong desire to do well. I put my daily routine aside to focus fully on the work. Thanks to the support of my colleagues—especially the development and infrastructure teams—we successfully renewed our certification, despite the rapid changes AI is bringing to regulatory processes. I’m enjoying the process of building up from the basics, based on my prior experience.

Working across teams this time gave me confidence in our collaboration, and it made me more optimistic about our global expansion. I'm also looking forward to welcoming new team members.

Shinjae described PROMEDIUS as “a long road ahead”—acknowledging how much lies ahead, but also expressing a strong sense of purpose and expectation for their role along the way. We’re proud to have such a dedicated professional who helps prove the value of our technology and products to the world.

Next up: Shinjae has passed the baton to Kyuwoon Jeong from our Marketing Team. They joined around the same time and Shinjae is curious to hear how Kyuwoon has been adapting. Stay tuned for the next story in our Relay Interview series!