The RefleXion® X1 is cleared for SBRT/SRS/IMRT. BgRT is pending regulatory review and is not commercially available.
cancer care • radiation therapy • life sciences • medical devices • biotechnology
May 9
🏢 In-office - Bay Area
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The RefleXion® X1 is cleared for SBRT/SRS/IMRT. BgRT is pending regulatory review and is not commercially available.
cancer care • radiation therapy • life sciences • medical devices • biotechnology
• Analyze and review product specifications to ensure testability. • Develop and document test protocols for manual test cases. • Develop and document test protocols for automated test cases. • Perform test case dry runs and work with developers to clarify intended functionality and identify deviations. • Execute formal verification test runs on configuration-controlled systems. • Interpret test results and identify & document encountered defects. • Work closely with other testers and developers to coordinate testing efforts and to resolve issues. • Other duties as assigned.
• Bachelor’s degree or its foreign equivalent in Software Engineering, Computer Science, or a related field and 8 years of experience as a software engineer, test engineer, or in a related occupation. • 5 years of experience in software testing. • 2 years of experience testing FDA Class II or Class III medical device software. • 2 years of experience testing PET imaging systems and PET emission sources. • 2 years of experience working with diagnostic images. • 2 years of experience working with Linux (Ubuntu) or equivalent Unix variant. • 2 years of experience writing and executing automated test scripts. • 2 years of experience with requirements-based testing. • 2 years of experience employing ALM tools for managing requirements, test, and issue tracking (e.g., HP/ALM, Helix, Rational, etc.). • 2 years of experience writing technical documentation for medical device design history files compliant with FDA 21 CFR Part 820.
• N/A
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