QA Automation Tester (Selenium/Playwright)
Eurofins Scientific (company site, opens in a new tab)2–5 yrsBengaluruHybridDirect career pageEst. 6–12 LPA
Posted 10h ago
Reach people at Eurofins Scientific
People at this company you can reach
Log in to see who works here
Create a free account or log in to see the people at Eurofins Scientific you could write to:
- Recruiters & HR
- People in this function
- Work addresses
Your match
Against your primary resume
Log in to see your match score
Create a free account or log in to unlock your CV match score across:
- Role fit
- Experience
- Industry relevance
Protocol Intelligence
How competitive this role is
Competition
Background fit
Strictness
Log in to see why each signal reads the way it does.
Job description
Structured overview of role & requirements
About This Role
- Own the design, development, and maintenance of test automation frameworks and suites to improve automation coverage and reduce manual effort.
- Lead quality assurance efforts including functional, integration, regression, and UAT testing to ensure defect-free LIMS applications in regulated BioPharma environments.
- Support release validation, defect management, and compliance activities ensuring documented evidence for regulated systems in an Agile setting.
Minimum Requirements
- 2-5+ years of experience in Software Quality Assurance with strong functional and regression testing skills.
- Hands-on experience with automation tools like Selenium, Playwright, or WebDriverIO; familiarity with API testing tools like Postman.
- Bachelor's degree in Engineering, Computer Science, or equivalent (MCA also acceptable).
- Experience in Healthcare, Life Sciences, Laboratory Systems, LIMS or regulated environments preferred but not mandatory.
Ideal Candidate Profile
- Proven track record improving test automation coverage and integrating automated tests into CI/CD pipelines in Agile teams.
- Experience collaborating cross-functionally with product, development, and QA teams and mentoring junior QA engineers.
- Comfortable handling release validation and evidence generation within regulated environments compliant to standards like GxP, GMP, or CSV.