Bayer AG
Software V&V Engineer - Testing (Mid) - App & Platfo
Bayer AG, Phila, Pennsylvania, United States,
Software V&V Engineer - Testing (Mid) - App & Platfo (Contract)
Contract (5 months 29 days)Published 3 days agoVerification & ValidationAutomation frameworksPython ProgrammingJob Summary:Join our Radiology Software Assurance & Operations Team to contribute to the verification and validation of software for cutting-edge medical devices. As a Software V&V Engineer, you will play a crucial role in ensuring that our products meet FDA design controls and exceed customer expectations through meticulous testing and analysis.Responsibilities:Verify and validate software for complex system interactions in medical devices, including application, embedded, platform, and operating system software.Develop and execute manual and/or automated software verification protocols, from requirement analysis to test case execution.Ensure the software platform of medical devices meets standards for user interface, performance, reliability, safety, and interoperability.Adhere to standard operating procedures for medical device development, including compliance with ISO 13485 and IEC 62304.Analyze technical situations, identify problems, and collaborate with cross-functional teams to find solutions.Participate in continuous improvement initiatives to enhance the Software Assurance function.Skills:Bachelor's degree in Engineering (Computer/Electronics/Electrical).Minimum of 5 years' experience in automated test script development and execution.Proficiency in Python programming/scripting.Experience with Automation framework development.Strong technical writing skills for various audiences.Ability to work on-site throughout the week.Qualifications:Experience designing medical device software under FDA Design Controls and ISO 13485/IEC 62304 guidelines preferred.Familiarity with tools like Rational Quality Manager, Jenkins, Squish, TOSCA, JIRA, Git, DOORS Next Gen.Knowledge of Windows/Linux operating systems.Ability to troubleshoot effectively and make informed decisions quickly.Excellent communication skills and team collaboration abilities.This is an exciting opportunity to be at the forefront of developing innovative medical technologies while working within a dynamic team environment. If you are passionate about ensuring quality in healthcare technology and enjoy problem-solving in a collaborative setting, this role is perfect for you. Join us in shaping the future of medical device software!
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Contract (5 months 29 days)Published 3 days agoVerification & ValidationAutomation frameworksPython ProgrammingJob Summary:Join our Radiology Software Assurance & Operations Team to contribute to the verification and validation of software for cutting-edge medical devices. As a Software V&V Engineer, you will play a crucial role in ensuring that our products meet FDA design controls and exceed customer expectations through meticulous testing and analysis.Responsibilities:Verify and validate software for complex system interactions in medical devices, including application, embedded, platform, and operating system software.Develop and execute manual and/or automated software verification protocols, from requirement analysis to test case execution.Ensure the software platform of medical devices meets standards for user interface, performance, reliability, safety, and interoperability.Adhere to standard operating procedures for medical device development, including compliance with ISO 13485 and IEC 62304.Analyze technical situations, identify problems, and collaborate with cross-functional teams to find solutions.Participate in continuous improvement initiatives to enhance the Software Assurance function.Skills:Bachelor's degree in Engineering (Computer/Electronics/Electrical).Minimum of 5 years' experience in automated test script development and execution.Proficiency in Python programming/scripting.Experience with Automation framework development.Strong technical writing skills for various audiences.Ability to work on-site throughout the week.Qualifications:Experience designing medical device software under FDA Design Controls and ISO 13485/IEC 62304 guidelines preferred.Familiarity with tools like Rational Quality Manager, Jenkins, Squish, TOSCA, JIRA, Git, DOORS Next Gen.Knowledge of Windows/Linux operating systems.Ability to troubleshoot effectively and make informed decisions quickly.Excellent communication skills and team collaboration abilities.This is an exciting opportunity to be at the forefront of developing innovative medical technologies while working within a dynamic team environment. If you are passionate about ensuring quality in healthcare technology and enjoy problem-solving in a collaborative setting, this role is perfect for you. Join us in shaping the future of medical device software!
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