Software Verification Engineer

Description The Kestra team has over 400 years of experience in the external and internal cardiac medical device markets. The company was founded in 2014 by industry leaders inspired by the opportunity to unite modern wearable technologies with proven device therapies. Kestra’s solutions combine high quality and technical performance with a wearable design that provides the greatest regard for patient comfort and dignity. Innovating versatile new ways to deliver care, Kestra is helping patients and their care teams harmoniously monitor, manage, and protect life. Responsible for implementing, maintaining, and executing automated and manual tests for software and system verification for multiple projects. Works collaboratively with development teams to identify and appropriately address design quality and reliability issues during development. Ensures compliance with all applicable Quality System requirements and the proper utilization of established best practices related to product-level software test. Produce complete, concise, clear and technically correct work outputs. Actively participate in and contribute to improvements to design assurance processes and tools. ESSENTIAL DUTIES Review and modify product design inputs for completeness, adequacy and testability Develop test cases that ensure software and system meets product requirements Develop, review, maintain and execute automated and manual software design verification protocols Configure and maintain test stations (e.g. computers, mobile devices, off-the-shelf and custom test fixtures) Create and track work tasks in project tracking software Create, track, and verify issues in our issue tracking system Compile software test results and create test reports Participate in product test improvement initiatives, and provide technical contributions for the evolution of product test best practices Work with limited supervision COMPETENCIES Passion: Contagious excitement about the company – sense of urgency. Commitment to continuous improvement. Integrity: Commitment, accountability, and dedication to the highest ethical standards. Collaboration/Teamwork: Inclusion of Team Member regardless of geography, position, and product or service. Action/Results: High energy, decisive planning, timely execution. Innovation: Generation of new ideas from original thinking. Customer Focus: Exceed customer expectations, quality of products, services, and experience always present of mind. Emotional Intelligence: Recognizes, understands, manages one’s own emotions and is able to influence others. A critical skill for pressure situations. Ability to be a self-starter, seek new and better methods, and work with minimum supervision. Ability to collaborate within a Team environment and across functions. Capability to discern relevant facts and in turn, effectively resolve issues by making good decisions (compliance, quality, integrity, ethics, and critical thinking ability). Ability to be flexible in a fast-paced goal-oriented environment. Demonstrates the understanding of deadlines and time limits, ability to accomplish goals, and the desire to win. Requirements QUALIFICATIONS Education/Experience Required: Bachelor’s degree or equivalent years of experience in computer science, engineering, or a related field 3+ years' experience in automated test or test infrastructure development (preferably in the medical device industry) Ability to write scripts in Python or other scripting language Preferred: Familiarity with automation software (e.g. Jenkins, GitLab CI) Familiarity with Linux Experience writing and executing detailed test cases, test plans, and test design documents Experience with issue and project tracking software (Jira or similar) Experience in an externally regulated product development environment (FDA, FAA, etc.) Familiarity with 21 CFR 820 regulations and ISO 13485, and 17025 medical device standards Strong technical writing skills and interpersonal communication skills WORK ENVIRONMENT Indoor open office environment Minimal noise volume typical to an office environment Extended hours when needed Kestra manufactures and provides life-saving products regulated by the Federal Food and Drug Administration and under contract with Medicare. Kestra maintains a drug free workplace and testing is a condition of employment. PHYSICAL DEMANDS Frequent repetitive motions that may include wrists, hands and/or fingers, such as keyboard and mouse usage Frequent stationary position, often standing or sitting for prolonged periods of time Frequent computer use Frequent phone and other business machine use Occasional lifting required, typically between 2-15 pounds TRAVEL Occasional travel may be required, less than 10% OTHER DUTIES: This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the Team Member. Duties, responsibilities, and activities may change or new ones may be assigned at any time with or without notice. Benefits Kestra offers a very competitive benefit package including Medical, Dental, 401K with Match, etc. Pay equity is an important part of Kestra’s Culture. Our compensation ranges are guided by national and local salary surveys and take into consideration experience level and internal equity. Each role is benchmarked based on the job description provided. If your qualifications and/or experience level are outside of the posted position, we encourage you to apply as we are growing fast and roles that are coming soon may not be posted. Salary: Annualized between $90,000 - $100,000, depending on experience and location. Kestra Medical Technologies is an equal opportunity employer. Kestra Medical Technologies does not discriminate on the basis of race, color, religion, national origin, veteran status, disability, age, sexual orientation, gender identity and/or expression, marital status, or any other characteristic protected by law. We are unable to sponsor or take over sponsorship of employment visas at this time. Applicants must be eligible to work for any employer in the U.S. Kestra manufactures and provides life-saving products regulated by the Federal Food and Drug Administration and under contract with Medicare. Kestra maintains a drug free workplace and testing is a condition of employment.