Healthcare QA Engineer | Automated Testing for Medical Apps

Grifols; Parets del Vallès; Ibrido; EUR 32.000 - 45.000; Tempo pieno

Vantaggi offerti da questo lavoro

Hybrid model

Flexible schedule

Location Parets del Vallès

Descrizione del lavoro

Grifols is seeking a Software QA Engineer to join its international team in Parets del Vallès. The role focuses on ensuring quality, reliability and compliance of blood typing analyser software through manual and automated testing.

You will collaborate with developers, execute diverse test types, document defects, and maintain testing documentation in a rapidly evolving, FDA-regulated environment. Hybrid work schedule is available.

Competenze

• CFGS or degree in CS/Telecommunications or related field.
• 1–3 years of software quality and testing experience.
• Hands-on experience with Java or JavaScript.
• Experience with Selenium, Playwright, Rest Assured, Cucumber or Gherkin.
• Strong teamwork and English communication (B2).
• Experience in agile/scrum and FDA-regulated environments is a plus.

Mansioni

• Collaborate with the development team to plan and refine upcoming work.
• Execute and maintain manual and automated test plans for blood typing analyser applications following quality policies.
• Identify and document bugs.
• Participate in functional, regression, smoke, exploratory and acceptance testing.
• Create and maintain technical documentation per quality standards.

Conoscenze

QA testing

Team collaboration

English communication

Agile/Scrum experience

Formazione

CFGS or higher degree in CS/Telecommunications

Strumenti

Selenium

Playwright

Rest Assured

Cucumber

Gherkin

Java

JavaScript

Descrizione del lavoro

Grifols is seeking a Software QA Engineer to join its international team in Parets del Vallès. The role focuses on ensuring quality, reliability and compliance of blood typing analyser software through manual and automated testing.

You will collaborate with developers, execute diverse test types, document defects, and maintain testing documentation in a rapidly evolving, FDA-regulated environment. Hybrid work schedule is available.