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This position was posted on May 7, 2026 and is likely no longer accepting applications. We've kept it here for historical reference. Check out the similar jobs below!

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Software Quality Engineer

Job Overview

Location

Costa Rica Remote

Job Type

Full-time

Category

Software Engineering

Date Posted

May 7, 2026

Full Job Description

đź“‹ Description

  • • As a Software Quality Engineer at Clario, part of Thermo Fisher Scientific, you will ensure the reliability, performance, and quality of enterprise-level software solutions that support clinical trials, diagnostics, and medical decision-making in highly regulated environments.
  • • You will design, execute, and maintain manual and automated test strategies, review requirements to define test scope, collaborate with engineers to troubleshoot defects, develop repeatable QA test plans, and investigate test failures across environments using logs and database queries to support root cause analysis.
  • • You will join a fast-paced Agile Quality Assurance team focused on driving quality throughout the software development lifecycle with strong emphasis on test automation, collaboration, and continuous improvement in a mission-driven organization improving patient outcomes worldwide.
  • • You will gain hands-on experience with cloud-based testing, DevOps practices, and AWS environments while developing expertise in regulated healthcare software systems and contributing to life-changing medical innovations.

🏖️ Benefits

  • • Competitive compensation
  • • Private medical and dental insurance
  • • Life insurance coverage
  • • Annual bonus (Aguinaldo) and statutory vacation
  • • Flexible remote work arrangements
  • • Employee wellness and development programs

Skills & Technologies

AWS
Remote
Degree Required

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About Clario

Clario is a global healthcare technology and services company that provides endpoint data solutions for clinical trials. It delivers imaging, cardiac safety, respiratory, eCOA, and precision motion technologies, supported by scientific and regulatory expertise, to help biopharmaceutical sponsors generate high-quality evidence and accelerate drug development.

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