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 th...