Senior Software Test Engineer LinkedIn Twitter Email Message Share Why Join Bracco Medical Technologies? At Bracco Medical Technologies, every employee has an impact on our Mission to empower lifesaving decisions. We create medical devices that give healthcare providers the insights they need to confidently and safely diagnose patients. Our unique line of products includes Intravascular Ultrasound (IVUS), Fractional Flow Reserve (FFR), Cardiovascular Imaging contrast delivery (CVi), and CT and MRI contrast delivery systems. Position Description Position Summary: The Senior Software Test Engineer will be an integral member of new product development team at BMT, focused on system software and integration testing for next generation cardiovascular and diagnostic medical devices. You will be responsible for designing, developing, and executing system software verification tests for medical devices, and analyzing software requirements and design specifications for testability. Primary Duties & Responsibilities: Work cross functionally to identify and define system and software requirements Analyze System and Software requirements to determine testability, completeness, and consistency Execute system software test planning and testing issue resolution during development to ensure that all medical devices are built in accordance with customer, business, and regulatory requirements. Perform ripple effect analysis for requirements and design level changes using technical standards, principles, theories, concepts, and techniques as they relate to software testing Develop test protocols by performing in-depth requirements analysis Assess the need to automate tests and develop either automated or manual test scripts Compile data and define changes required in testing equipment, testing procedures, or new testing requirements. Execute automated and manual test protocols following established procedures and capturing appropriate objective evidence Report and investigate observations and defects, working with other members of the development team to establish root cause and options for correction Provide and manage traceability evidence between requirements, tests, and risk documentation Write formal test plans and reports that can be used in submission packages to regulatory agencies Provide leadership and execution of best test method practices as part of a project team. Follow established standard operating procedures Qualifications (Knowledge, Skills & Abilities): Qualifications (Knowledge, Skills & Abilities): Minimum Bachelor's Degree in Engineering, Software, Computer Science, or related discipline or equivalent experience 5+ years of similar experience, including software testing and verification experience and/or software development experience Familiarity with electromechanical systems, sensors, control and data acquisition systems development Ability to grow productive, trusting, and open relationships with functional partners Strong interpersonal and communication skills High degree of organizational skills and high attention to detail Ability to handle multiple tasks and prioritize effectively Ability to work both independently and as part of a team Ability to develop protocols, conduct system tests and write reports Strong initiative, high energy, and passion about new technologies Proficient with MS Suite (Word, Excel, Outlook) Preferred: Graduate degree in Engineering (SW, EE, ME, or Systems Engineering) or another scientific discipline. 8+ years of product development experience Experience in the Medical Device or other regulated industry and knowledge of FDA QSR Experience with automated software test tools and techniques on desktop, mobile and cloud-based systems Tools: TestComplete, Python, PyTest, Selenium, Appium, WinAppDriver, Jira, Bitbucket, and Jama Other: Adheres to all company policies, procedures and business ethics codes and ensures that they are communicated and implemented with the team. Ability to travel up to 10% of the time Job Location 7905 Fuller Road, Eden Prairie, Minnesota Tracking Code 1351-432 ACIST Medical is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.