Quality Engineer

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 Sunquest 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