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Join us as one of the next two Software Quality Manual Test Analysts and help ensure the safety, quality, and reliability of breakthrough digital health solutions and clinical trial delivery systems that make a real difference to patients’ lives. As part of our Software Quality Assurance (SQA) team, you’ll play a key role in verifying and validating software across both Software as a Medical Device (SaMD) and pharma delivery projects (clinical trials).
Job Responsibility:
Liaise with Software Design Engineering and Product teams to ensure requirements are documented, and understood, implemented and independently verified
Prepare and maintain project documentation including test plans and reports for regulatory submissions
Write, review and execute test cases based on the product requirements
Support troubleshooting, defect triage, and root cause analysis
Requirements:
Bachelor’s degree in a relevant field (e.g. Software Development, IT, or similar) or equivalent experience
Understanding of the software development lifecycle and agile methodologies
Strong regulatory documentation skills
Nice to have:
Experience writing and executing test cases or UAT scenarios
Experience in medical device or pharmaceutical software testing
Experience working on SaaS based products
Familiarity with ISO 13485, IEC 62304, or related quality standards
ISTQB Foundation certification
Experience using Matrix Medical, JIRA and Confluence systems