Description:

• The Software Verification Engineer  will provide testing to Abbott’s Electrophysiology (EP) software verification team.
•  This motivated and resourceful individual will have input into the day-to-day impact of defects, workflow and software application associated with electrophysiology capital equipment systems.
•  Responsibilities include requirements analysis, test design, test data creation, test execution, defect issue resolution, Linux & Python script creation, debugging code and configuration test systems.

Primary Responsibilities:

• Work independently and as a team member to plan, write, and execute test cases according to Abbott practices, FDA regulatory, and ISO standard procedures.
• Participate in the requirements, hazard analysis, and design reviews for new features.
• Design new test suites for new features and functionality.
• Provide verification and validation perspective to R&D’s ongoing product development: requirements, product and test designs defect reviews, user workflows, and field complaint investigations
• Support implementation, enhancements, and modifications to test automation framework, automation tools, emulators, test scripts, and code.
• Identify parameters, structure, and critical test components
• Write, update, or execute test design cases, as well as procedures, and report results
• Perform dry runs and formal Verification activities as required
• Setup and configure Test Equipment
• Create and update Linux and Python scripts and execute them
• Record and close defects found during V&V activities
• Develop and maintain testing artefacts and other documents 
• Contribute to development of solutions that have significant improvements of processes and test development.
• Develop continuing proficiency in the field of software test engineering.

Required Qualifications:

• Bachelor’s Degree in Engineering (Computer, Electrical, or Software), Computer Science, or related discipline.
• 2+ months of professional software test engineering experience
• Experience with software development lifecycle management tools
• Organized, on-time, and detailed project management skills, including project leadership.
• Experience with Windows and LINUX operating systems.
• Strong technical skill set, including spreadsheet, word processing, PowerPoint and specialized applications
• Excellent documentation skills in delivering information that adds value to the management’s decision-making process

Preferred Qualifications:

• 2+ months of FDA regulated industry experience
• Experienced in quantitative, analytical, organizational, and follow-up skills
• Polished communicator - written documentation and oral presentations/ discussions/ meetings.
• Excellent reputation for building relationships across various levels of an organization.
• Organized, on-time, and detailed project management skills
• Energized attitude, proactive thinker and self-starter.