Better Care is a pioneering company that is leading the way in the collection, management and processing of clinical data. Founded in 2010 as a spin-off of the Parc Taulí University Hospital in Sabadell (Barcelona, Spain), it is growing with the support of healthcare professionals to meet their real needs.
What is the challenge? The large volume of data that healthcare professionals must manage makes it a challenge to understand and interpret in real time the multiple signals and parameters generated by medical devices connected to patients.
Our mission:
to connect knowledge for a better care
Our vision:
to be world leader in the digital transformation of clinical data, generating value for the healthcare system
We are passionate about innovation, we strongly believe that we can always improve and we strive to understand the healthcare needs and respond to them.
If innovation, technology and entrepreneurship are something you enjoy, be part of our project!
The Role:
We are seeking a Quality Assurance (QA) Engineer for our Engineering department. The main goal of the QA Engineer will be to ensure the quality and safety of our products. This role will work collaboratively between the Engineering and Product teams, ensuring compliance with regulatory requirements and quality standards in the medical device sector.
Key Responsibilities:
* Design, develop, and execute test plans to validate the functionality, usability, performance, and security of medical software
* Implement and maintain automated and manual testing
* Ensure compliance with applicable regulatory standards (ISO 13485, IEC 62304, FDA, MDR, ENS, ISO 27001)
* Collaborate with Engineering and Product teams in identifying, documenting, and resolving defects
* Define and implement quality metrics and best practices for software development
* Participate in code and design reviews to ensure quality practices are followed
* Generate test reports, document defects, and track incidents
* Support internal and external audits related to quality assurance
* Stay up to date on regulations and trends in medical device software QA
* Develop product documentation, maintain, and update software versions
* Identify areas for improvement and propose new developments
Your profile:
* Degree in Systems Engineering, Software Engineering, Biomedical Engineering, or a related field
* Knowledge of testing methodologies (functional, regression, integration, stress, and automation testing)
* Experience with test automation tools (Selenium, Cypress, JUnit, TestNG, or others)
* Familiarity with CI/CD and continuous integration tools (Jenkins, GitLab CI/CD, Azure DevOps)
* Understanding of medical software regulations (ISO 13485, IEC 62304, FDA 21 CFR Part 11, MDR, ISO 27001, ENS high level)
* Experience with test management and defect tracking tools (JIRA, TestRail, Zephyr, Xray, among others)
* Knowledge of Agile methodologies (Scrum, Kanban)
* Strong analytical skills, attention to detail, and problem-solving mindset
* Intermediate-advanced English proficiency (technical reading and writing)
Nice to have:
* QA certification (ISTQB or equivalent)
* 3 years of experience in software quality assurance
* Experience in validation and verification of medical software
What is in for you at Better Care?
People are our engine and we strongly believe that the best talent deserves the best work culture, that's why we offer unique perks & benefits: