Design system & performance testing for complex algorithms to verify the design output
Draft testing protocols and reports
Lead testing projects under design control procedure
Perform basic statistical analysis on collected data and present results
Execute test cases following system test plans to ensure product compliance with applicable standards.
Work according to the full product lifecycle including design, testing, documentation, and ECOs implementation.
Conduct risk assessments to identify potential software hazards and ensure appropriate mitigation measures are in place.
Develop and execute test cases, test scripts, and test procedures to verify software functionality, performance, and usability.
Establish and maintain traceability matrices, ensuring that requirements are properly tested and documented.
Collaborate with Product Management, VP R&D, and software development teams to identify and resolve software defects and performance issues.
Champion the use of best practices, industry standards, and regulatory requirements for software quality assurance
Conduct root cause analysis and drive corrective actions for software defects and non-conformities.
Participate in design reviews, software hazard analysis, and risk management activities.
Provide leadership, guidance, and mentoring to junior members of the QA team.
Stay updated with the latest industry trends, tools, and technologies related to software quality assurance in the medical device domain

Bachelor's or master’s degree in computer science, Software Engineering, or a related field.
2 years of experience in System V&V or software quality assurance, preferably in the medical device industry.
Strong knowledge of software development life cycle (SDLC) methodologies, software testing principles, and QA best practices.
Experience with mobile and web manual testing
Experience working with API Testing*Proficiency in test case design, test execution, defect management, and test management tools.
Familiarity with software verification and validation processes, including test plan development, test case creation, and test result analysis.
Strong analytical, problem-solving, and troubleshooting skills, with a keen attention to detail.
Excellent communication and collaboration skills, with the ability to work effectively in cross-functional teams.
Highly self-motivated, independent, and ability to work under pressure in a fast-paced start-up environment
Experience in the usage of coding/scripting languages – an advantage
Solid understanding of regulatory requirements for software as a medical device (e.g., FDA 21 CFR Part 820, ISO 13485, IEC 62304) – advantage.
Experience with risk management methodologies, including software hazard analysis and risk mitigation strategies – advantage.
Experience in automation platforms (Appium, Selenium, JUnit, etc.) – an advantage

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