Quality Engineer (Medical Software)

Barcelona, Cataluña, España | QARA | Full-time | Fully remote


QMENTA was founded to empower the breakthroughs that will ultimately make brain diseases a thing of the past. We deliver on our vision by serving as the indispensable hub for data, tools, and expertise that accelerates the understanding, diagnosis and treatment of CNS disease. How? We bring to market a powerful package of sophisticated technologies integrated into a single software solution that easily fuses big brain data with AI analytics.

As a Quality Engineer, you will be responsible to ensure our software is of the highest quality and compliant with our Quality Management System (QMS). You will be working side by side with other experts on our team to deliver testing tools and solutions to help identify issues across our product offerings.


  • Estimate, prioritize, plan and coordinate quality testing efforts included in the medical software lifecycle.
  • Design, implement, and integrate testing solutions into a continuous integration/delivery pipeline.
  • Perform end-to-end tests manually to validate the front end functionality.
  • Support user acceptance testing.
  • Review requirements, specifications and technical design documents to provide timely and meaningful feedback according to the QMS.
  • Assist in the first line customer support and the management of claims, Non-conformities, CAPAs, and software issues.


  • Mid-Senior level: At least 3 years of professional experience as a Quality Engineer, ideally in medical software. 
  • Experience in the software development life cycle in a regulated environment, ideally in the Healthcare sector.
  • Experience working in a CI/CD environment (e.g. Jenkins).
  • Experience in Cloud environments.
  • Excellent verbal and written communications skills in English.
  • Independent reasoning and critical thinking skills.


  • Experience working in an Agile environment.
  • Experience building and maintaining Test Automation Frameworks for web applications and APIs using tools like Selenium or Katalon studio.
  • Experience in regulatory standards such as ISO 13485, IEC 62304, and/or 21 CRF Part 820 (FDA).
  • Documentation in Jira and Confluence.


  • Mid-Senior salary 35K€-45K€.
  • Remote Work.
  • Opportunities for growth.
  • Opportunity to work on fascinating challenges that improve people’s lives.

We are looking forward to your application!



At QMENTA, we strive to solve hard problems with creative solutions, and have fun during the process. In everything we do, we’re guided by our ABCDE’s core values:


  • Positiveness: We face challenges with a positive attitude.
  • Encourage: We work hard and share your enthusiasm.
  • Amplify: We amplify our capabilities and multiply results.


  • Brains before brawn: We are resourceful and innovative.
  • Proactive: We generate constructive change both personal and professional.
  • Pride: We take pride in our work and recognize it.


  • Ambition: We tackle important and meaningful problems.
  • Impact: We are making a difference in the world.
  • Excellence: We set the bar high.


  • Fast delivery: We are nimble and efficient.
  • Quality: We understand our clients and deliver the highest quality product.
  • Accountability: We are pragmatic and meet our commitments.


  • Privacy and Security: We design our systems to protect data following global industry standards.
  • Expertise: We have the knowledge and skills to solve your problems.
  • Trust: We are honest, ethical and our word is our bond.

Only CVs in English will be taken into consideration.

We are an exciting and rapidly growing business where everyone works hard towards a common goal of exceeding customer expectations. We are looking for the right candidate to join us on our journey.