עדיין מחפשים עבודה במנועי חיפוש? הגיע הזמן להשתדרג!
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.
מלאה
14,000-19,000 ₪
We are seeking a highly motivated V&V Automation Engineer to design, develop, and maintain automated test solutions for our cutting-edge medical imaging products. This role involves ensuring the quality and reliability of our software and systems through robust and efficient automated validation and verification processes.
Job Responsibilities
Design, develop, and implement automated test scripts and frameworks for complex medical devices and software applications.
Collaborate with development, V&V, and product teams to understand system requirements, design specifications, and test cases.
Perform comprehensive verification and validation activities, including functional, performance, security, and regression testing.
Analyze test results, identify defects, and work closely with development teams to ensure timely resolution.
Maintain and enhance existing automation infrastructure, tools, and processes to improve efficiency and coverage.
Develop and execute test plans, test cases, and test procedures in accordance with regulatory standards (e.g., ISO 13485, FDA 21 CFR Part 820).
Document test activities, results, and defects accurately and thoroughly.
Participate in design reviews and provide feedback on testability and automation potential.
Stay up-to-date with industry best practices in test automation, software development, and medical device regulations.
Job Responsibilities
Design, develop, and implement automated test scripts and frameworks for complex medical devices and software applications.
Collaborate with development, V&V, and product teams to understand system requirements, design specifications, and test cases.
Perform comprehensive verification and validation activities, including functional, performance, security, and regression testing.
Analyze test results, identify defects, and work closely with development teams to ensure timely resolution.
Maintain and enhance existing automation infrastructure, tools, and processes to improve efficiency and coverage.
Develop and execute test plans, test cases, and test procedures in accordance with regulatory standards (e.g., ISO 13485, FDA 21 CFR Part 820).
Document test activities, results, and defects accurately and thoroughly.
Participate in design reviews and provide feedback on testability and automation potential.
Stay up-to-date with industry best practices in test automation, software development, and medical device regulations.
Requirements:
Bachelor's degree in Computer Science, Software Engineering, Electrical Engineering, or a related technical field.
2+ years of experience in software V&V and test automation, preferably within the medical device industry.
Proficiency in at least one object-oriented programming language (e.g., C#, Python, Java).
Experience with test automation frameworks and tools (e.g., Selenium, Playwright, Cypress, Squish, TestComplete).
Strong understanding of software development lifecycle (SDLC) and various testing methodologies.
Familiarity with regulatory standards for medical devices (e.g., IEC 62304, ISO 14971, FDA guidelines) is a significant advantage.
Experience with version control systems (e.g., Git).
Excellent analytical, problem-solving, and debugging skills.
Strong communication and collaboration skills, with the ability to work effectively in a cross-functional team environment.
Proactive and self-motivated with a strong commitment to quality and attention to detail.
Bachelor's degree in Computer Science, Software Engineering, Electrical Engineering, or a related technical field.
2+ years of experience in software V&V and test automation, preferably within the medical device industry.
Proficiency in at least one object-oriented programming language (e.g., C#, Python, Java).
Experience with test automation frameworks and tools (e.g., Selenium, Playwright, Cypress, Squish, TestComplete).
Strong understanding of software development lifecycle (SDLC) and various testing methodologies.
Familiarity with regulatory standards for medical devices (e.g., IEC 62304, ISO 14971, FDA guidelines) is a significant advantage.
Experience with version control systems (e.g., Git).
Excellent analytical, problem-solving, and debugging skills.
Strong communication and collaboration skills, with the ability to work effectively in a cross-functional team environment.
Proactive and self-motivated with a strong commitment to quality and attention to detail.
This position is open to all candidates.
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.
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