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Senior niche QA role at a strong brand in metro increases medium applicant density.
Regulated medical-device verification and standards knowledge makes cross-industry transferability low, so sensitivity is high.
Explicit 10+ years requirement plus regulated medical-device standards and tool mandates increases strictness.
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Lead and manage the software verification team to design and execute test strategies and verification environments for product software, ensuring coverage and performance requirements are met.
Drive the development and documentation of test cases, coordinate debugging with design teams, and own risk identification and mitigation for testing activities.
Oversee verification activities through the software development lifecycle (SDLC) including reporting, ensuring delivery of verified design blocks for sign-off within an Agile team setting.
Bachelor's or Master's degree in Computer Science, Computer Engineering, Electrical Engineering, Software Engineering or related field.
10+ years of related experience in software verification or quality assurance, preferably with regulated products like medical devices or aviation software.
Experience with executing comprehensive verification strategies including functional, non-functional, reliability, and performance testing.
Experience working in Agile/Scrum development processes.
Senior engineer with leadership experience managing small to medium technical teams in software verification, preferably within regulated environments such as medical device software development.
Proficient in designing test architectures and automation frameworks, with hands-on exposure to tools like ALM, JIRA, and preferably Selenium.
Strong collaboration skills demonstrated by experience working effectively in global and cross-functional teams, capable of guiding test strategy and risk mitigation.