At LEX, we’re developing current and next generation diagnostic instruments that help customers make better, faster decisions.
Joining the team at LEX offers a rare and exciting opportunity to be part of a company that has successfully achieved FDA 510(k) approval with CLIA waiver. A significant milestone that many early stage diagnostic companies strive for, but few accomplish.
Securing regulatory approval is an exceptional achievement, requiring our team to have deep expertise in product development, quality systems, clinical validation, and regulatory strategy. Being part of the team that took their first device across the regulatory finish line means you’ll work alongside professionals who understand exactly what it takes to transform innovative science into a market ready, compliant point of care diagnostics. For your career, our environment provides invaluable exposure to real world regulatory success, accelerated learning, and the chance to contribute to the next generation of diagnostic technologies.
Based onsite at our Melbourn, (just south of Cambridge) offices, you’ll join a perfectly formed collaborative, multidisciplinary engineering team.
This isn’t just another design job. You’ll take concepts from high level requirements through to real world, manufacturable products.
You’ll be trusted, supported, and encouraged to innovate.
What you’ll be doing
Requirements
You don’t need every box ticked, but here’s what we are looking for
Desirable experience
What success looks like
You’ll thrive if you enjoy solving complex engineering challenges and taking ownership of your designs. This is a fast-paced environment where “right first time” design is valued, but you’ll have supportive and experienced colleagues around you who all work together to solve problems.
How you’ll grow
Benefits
Ready to build something meaningful?

LEX Diagnostics is a privately held molecular diagnostics company transforming point-of-care testing through its proprietary ultra-fast thermal cycling technology. Designed to deliver lab-quality PCR results directly from a swab sample in minutes, the VELO system bridges the gap between accuracy and accessibility, empowering healthcare professionals to make informed clinical decisions faster.