16033 - V&V Engineer

Qualitest, the World’s Leading AI-Powered Quality Engineering Company

At Qualitest we're all about ensuring everything runs smoothly, whether it's your business, technology, or operations. We leverage smart engineering-led practices and precise processes to maintain excellence in all that we do.

Our clients are the world’s top brands and our diverse global team of 8,000 employees, including 1,500 in Israel, collaborates with industry leaders in technology, finance, insurance, and beyond, making a significant impact in the world of technology.

We offer creative and flexible solutions to ensure the quality of your business operations, safeguarding your brand's reputation. We're proud to say we've been pushing the boundaries for over 25 years now, always striving for innovation and delivering exceptional service.

Ready to make a difference? Join our dynamic and forward-thinking team!

We seek a System V&V Engineer to join our dedicated team. As a System V&V Engineer, you will lead the system, algorithm, and SW testing efforts for our software products, including mobile, server, and web. Ensuring that they meet the highest performance, quality, and compliance standards. You will collaborate closely with cross-functional teams, including Product managers, Algorithm Lead, software developers regulatory affairs, and clinical experts to drive the successful execution of our V&V testing

This is a full-time, on-site position located in Or Yehuda.

Responsibilities

• 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

Requirements

• 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

Why should you join us?

• Recognized among Israel's top 100 best places to work for, four years in a row
• Be part of a company that is a globally recognized leader in Quality Engineering
• Experience our team spirit, working with real people, and solving real challenges
• Work with Senior Specialists and Practice Experts. · Nurture your personal and professional growth through tailored career paths
• Dive into interesting projects using cutting-edge technology designed by and for Quality Engineers
• Enjoy unique placement opportunities worldwide
• We believe in a workplace culture that values open communication and fairness, encouraging our employees to feel seen, supported, and empowered to realize their full potential