Responsibilities
* Collaborate with the development team to plan and refine upcoming work.
* Execute and maintain manual test plans for blood typing analyzer applications following the established quality policies and standards.
* Design both manual and automated software test plans in the field of in vitro analyzers.
* Identify and document bugs.
* Participate in various types of testing, including functional, regression, smoke, exploratory and acceptance.
* Create and maintain the technical documentation following the established quality policies and standards.
Qualifications
* You have a Certificate of Higher Education (CFGS), a degree or master’s in computer science, Telecommunications or other relevant degree.
* You have at least 1 year of experience in software quality & testing using technologies such as Selenium, REST‑assured, Cypress, Playwright or similar.
* You have knowledge working with at least one object‑oriented programming language such as Java, .NET or similar.
* You are knowledgeable in agile methodologies such as SCRUM.
* You are highly motivated to work collaboratively with the team to deliver a high‑quality product to our customers.
* You are an open‑minded, positive, pragmatic and team player.
* You can communicate openly and clearly in English (B2 level).
* Having experience working in an agile/scrum environment is a plus.
* Having experience working in FDA regulated environments is a plus.
* Experience with tools like Jama or DOORs is a plus.
Benefits
* Contract of Employment: Permanent position
* Flexibility for U Program: Hybrid
* Location: Parets del Vallès
* Flexible schedule: Monday‑Thursday 7‑10 to 16‑19h and Friday 8‑15h (with the same flexibility start time)
Equal Opportunity
We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. Grifols is an equal opportunity employer.
#J-18808-Ljbffr