Job Description

Purpose As a Quality Engineer, you will work with a fast-paced and multi-functional Agile development team to build software for precision medicine that will use genetics to diagnose hereditary diseases and cancer treatment plans. As a member of the development team, your focus will be on identifying real-world, user-centric scenarios and workflows and building & executing test plans to ensure their accuracy. Additionally, you will be responsible for reporting, tracking, and testing issues discovered during design and development. Essential Functions Works with Agile team in identifying scenarios and workflows to best represent client usage of the application Assist in requirements and design reviews for functional accuracy Develop, execute, and document test plans to ensure the product we produce is accurate Analyzes defects, performs root cause analysis, and collaborates with others to resolve issues Identifies testing risks and implements mitigations to build a quality product within the established delivery timeline Recommends, schedules, and facilitates cross-department testing events to ensure application quality Develop persona analyses for persona-based roles testing Drives clarity and understanding of new features by actively considering and utilizing scenarios that are beyond acceptance criteria and team discussion All other duties and responsibilities as assigned Skills needed to be successful Strong analytical abilities Solid automated testing skills (selenium) and knowledge of quality processes Ability to assimilate new product knowledge quickly and easily Ability to accurately estimate task durations and complete work projects as scheduled Clear, effective verbal and written communication skills Required Experience & Education Bachelor s degree in Engineering or related discipline or equivalent relevant work experience 2-4 years experience in quality engineering 2-4 years of testing experience or other applicable Clinisys experience 2-4 years working with current Quality Assurance standard methodologies, and tool sets. Preferred Experience & Education Knowledge of FDA medical device regulatory practices a plus Knowledge and/or experience with genetics, wet labs, or healthcare software a plus Supervisory Responsibilities None