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Your role:
Develop and execute test plans, test cases, and test scripts for embedded software applications in medical devices.
Conduct manual testing of embedded software for medical devices, ensuring compliance with regulatory standards and requirements.
Design, develop, and maintain automated test frameworks and scripts to streamline testing processes.
Collaborate with cross-functional teams to identify software defects, troubleshoot issues, and drive resolutions.
Perform code reviews to ensure code quality, adherence to coding standards and best practices.
Analyze test results and provide clear and concise reports to stakeholders, including recommendations for improvements.
Document test results, defects, and test procedures accurately and comprehensively.
Stay updated on industry best practices, standards, and regulatory requirements related to medical device software testing.
Participate in cross-functional meetings and contribute to the overall product development lifecycle.
This is a hybrid role based out of Pittsburgh, PA.
You're the right fit if:
You have experience in manual testing, including test case design, execution, and defect tracking and hands-on experience with test automation tools and frameworks. Experience working with medical devices is preferred.
Your skills include proficiency in programming languages such as Python, C, C++, and/or C#. C# - object oriented experience is particularly desired for test automation.
You have a strong understanding of software testing principles, methodologies, and techniques and familiarity with software development lifecycle (SDLC) processes and methodologies (e.g., Agile, Scrum).
You have a Bachelor's degree in Computer Science, Electrical Engineering, or related field.
You have excellent problem-solving skills and attention to detail, and you have effective communication skills with the ability to collaborate across multidisciplinary teams.
Knowledge of regulatory standards and guidelines for medical device SW development and testing (e.g., FDA 21 CFR Part 820, IEC 62304, IEC81001-5-1, ISO 13485, EU Medical Device Directive (MDD) Compliance, EU Medical Device Regulations (MDR) compliance is preferred.
You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.
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If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion .
US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.
be provided for this position. For this position, you must reside inwithin commuting distance to Pittsburgh, PA
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