Costa Rica MedTech

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Gowned technicians assembling and inspecting medical devices in a clean, modern Costa Rica manufacturing lab.

Welcome to Costa Rica MedTech

Hi, I’m Leo Jiménez.

What I do

  • Engineering manager and program leader based in San José.
  • 15+ years delivering cross-functional work in regulated environments, including medical devices and safety-critical aerospace.

Why I’m sharing this

Costa Rica’s MedTech sector is already doing world-class work, and I want to help document where we are today and where we can go next. I’m sharing this page with humility, as a snapshot that will improve over time.

What you’ll find here

  • A growing guide to the companies building medical devices in Costa Rica.
  • A spotlight on the people behind the work: engineers, operators, quality and regulatory teams, supply chain leaders, and researchers.

How you can help

If you have a company or a team you think should be highlighted, write to us and we will make sure to bring your story to life.

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Managing Change in Regulated MedTech Software

🧭 TL;DR Who this article is for This article is for MedTech project managers, product managers, software leads, QA/RA, systems engineers, cybersecurity leads, and supplier-quality partners working with regulated software, SaMD and SiMD, connected devices, or hybrid medical-device programs. It is especially useful for teams trying to reconcile two pressures that often feel opposed: How…

Stakeholder Management in MedTech

Stakeholder management in MedTech is not a “soft skill.” It is part of the design-control and risk-control system that determines whether a product can be safely released, adopted, supported, and defended with objective evidence. This article is MedTech-first and experience-based. In regulated medical software, stakeholder management is not just communication. It is how expectations become…

Unpacking the Project Performance Domains

Project performance domains are one of those concepts that sit quietly underneath everything in modern project management: they’re not a “method,” but they often determine whether the work is coherent, repeatable, and value-realizing. I’m writing this from the perspective of a program manager in high‑stakes engineering (MedTech and other regulated environments). I started learning with…

From Sand to Silicon: Semiconductor Materials, Purification, Wafers, Films, and Dopants

Semiconductors are one of those fields where materials science and electronics meet in the most practical way: what a material is (and how clean, ordered, and intentionally “imperfect” it can be made) ultimately determines what circuits can do. I’m writing this series as an electronics engineer, and because earlier in my career I had the…

Agile in regulated medical device software: what TIR45:2023 really added

I believe in starting an Agile roadmap from an agnostic Agile perspective. I focus on the outcomes. I focus on flow. I focus on learning. I do this in any industry. I do it even more in safety-critical industries. That is why I paid close attention to the updates in AAMI TIR45:2023. This update matters.…

Laura López: The Economist Behind Costa Rica’s MedTech Boom

Laura López: The Economist Behind Costa Rica’s MedTech Boom You may know that Costa Rica has become a MedTech powerhouse but do you know that behind all these engineers and managers there is an economist thought leader helping shape the conditions for this economic miracle in the Americas? Laura López, CEO of PROCOMER (Costa Rica’s…

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