Verification and Validation

At IF MedTech, we are dedicated to revolutionizing healthcare through cutting-edge medical device design, development, and pilot manufacturing. Our global team collaborates with experts across medical, engineering, business, and research domains to bring innovative solutions that enhance healthcare and improve lives. Join us in our mission to drive innovation and make a global impact in the medical technology sector.

Responsibilities

● Develop and execute verification and validation protocols for medical device hardware and associated mobile and web applications.

● Design and set up testing environments for hardware and software components of medical devices.

● Perform functional, performance, and usability testing for software and hardware components.

● Identify and document defects and inconsistencies, collaborating with development teams for resolution.

● Design, implement, and execute automated test scripts for software applications where applicable.

● Assist in defining test strategies, test plans, and acceptance criteria for hardware and software systems.

● Ensure compliance with industry regulations such as ISO 13485, IEC 62304, and FDA guidelines.

● Contribute to the preparation of detailed test reports and validation documentation.

● Maintain testing tools and environments, ensuring readiness and calibration.

● Provide inputs for risk assessment and design reviews during product development.

● Maintain testing tools and equipment, ensuring calibration and readiness for testing.

● Stay updated with advancements in testing tools, automation frameworks, and industry best practices.

Qualifications

● Bachelor's degree in Biomedical Engineering, Computer Science, Electronics, or a related field.

● Preferably 0 to 2 years of experience in verification, validation, or quality testing, preferably in the medical device or software development domain.

● Ability to design and implement testing setups for hardware and software.

● Knowledge of industry standards such as ISO 13485, IEC 60601, IEC 62304, and FDA guidelines.

● Experience with documentation for regulatory submissions is advantageous.

● Familiarity with automated testing tools like Selenium, Appium, or similar frameworks is preferred.

● Proficiency in defect tracking tools (e.g., JIRA) and version control systems (e.g., Git).

● Strong analytical, problem-solving, and attention-to-detail skills.

● Excellent documentation and communication skills.

● A collaborative mindset with a proactive approach to problem-solving.

Join IF MedTech to drive innovation in healthcare technology and develop software solutions that transform lives worldwide!