About Cleerly

We’re Cleerly – a healthcare company that’s revolutionizing how heart disease is diagnosed, treated, and tracked. We were founded in 2017 by one of the world’s leading cardiologists and are a growing team of world-class engineering, operations, medical affairs, marketing, and sales leaders. We raised $223M in Series C funding in 2022 which has enabled rapid growth and continued support of our mission. In December 2024 we received an additional $106M in a Series C extension funding. Most of our teams work remotely and have access to our offices in Denver, Colorado, New, York, New York, Dallas, Texas, and Lisbon, Portugal with some roles requiring you to be on-site in a location.

Cleerly has created a new standard of care for heart disease through value-based, AI-driven precision diagnostic solutions with the goal of helping prevent heart attacks. Our technology goes beyond traditional measures of heart disease by enabling comprehensive quantification and characterization of atherosclerosis, or plaque buildup, in each of the heart arteries. Cleerly’s solutions are supported by more than a decade of performing some of the world’s largest clinical trials to identify important findings beyond symptoms that increase a person’s risk of heart attacks.

At Cleerly, we collaborate digitally and use a wide variety of systems. Our people use Google Workspace (GMail, Drive, Docs, Sheets, Slides), Slack, Confluence/Jira, and Zoom Video, prior experience in these areas is a plus. Role or department specific technology needs may vary and will be listed as requirements in the job description.

About the Opportunity

You’ll be responsible for maintaining and confirming the quality of Cleerly’s products and ensuring that the medical device conforms to and complies with company requirements, international standards, and federal regulations. You’ll work closely with our data science and product development teams to identify risks, design and implement risk management and mitigation strategies, identify software issues and track resolutions, participate in hazard analysis and develop and improve test strategies. On any given day you could be doing one of the following:

Developing the test plan and test cases for a new feature
Automating the world with Cypress.io or another framework
Contributing to our CI/CD pipeline and capabilities
Building complex test data sets
Manual test case execution
Participating in hazard analysis in compliance with ISO 14971
Exploratory testing of the application
Building a load testing suite for our backend systems
Testing backend APIs and services in a distributed system environment
Performing code reviews and driving bug triage
Participating in sprint planning and design meetings to help deliver quality at the earliest stages

TTC: $138,000 - 151,000

*Total Target Compensation (TTC): Total Cash Compensation (including base pay, variable pay, commission, bonuses, etc.). We hire employees anywhere within the United States and account for geography when determining base salary.

Requirements

Bachelor’s degree in Computer Science, Engineering, or equivalent experience preferred
3-5 years of quality experience ideally with a software as a medical device
Experience with fast-paced agile product development using JIRA
Excellent command of the English language with ability to draft and revise QMS documents with consistency of format and language.
A passion for quality assurance and experience building BDD test cases and scenarios
Experience automating full test suites with Cypress.io and/or other modern test frameworks
Prior usage of JMeter and Postman or equivalent tools
Solid knowledge of Javascript and SQL
Experience with vulnerability testing and cybersecurity
Experience testing SaaS applications in the cloud, preferably using AWS
Demonstrable ability to drive and measure quality metrics
Passion for working in a start-up company culture
Capability to document regulatory compliant verification test protocols and reports prior to regulatory submissions and product launch to ensure software fulfills functional requirements and meets user needs

Bonus:

Prior work history in Digital Health
Experience with Quality Systems pertaining to software as a medical device (SaMD)
Knowledge of ISO13485, 21 CFR 820, IEC 62304, ISO 14971, and AAMI TIR45
Experience conducting post-market surveillance activities, including field issue evaluation, complaint investigations, CAPAs, and NC
Strong understanding of risk management in medical device design, software development in product development, and post-market surveillance
Previous experience automating E2E across a distributed system

Working at Cleerly takes HEART. Discover our Core Values:

H: Humility- be a servant leader
E: Excellence- deliver world-changing results
A: Accountability- do what you say; expect the same from others
R: Remarkable- inspire & innovate with impact
T: Teamwork- together we win

Don’t meet 100 percent of the qualifications? Apply anyway and help us diversify our candidate pool and workforce. We value experience, whether gained formally or informally on the job or through other experiences. Job duties, activities and responsibilities are subject to change by our company.

OUR COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER. We do not discriminate on the basis of race, color, national origin, ancestry, citizenship status, protected veteran status, religion, physical or mental disability, marital status, sex, sexual orientation, gender identity or expression, age, or any other basis protected by law, ordinance, or regulation.

By submitting your application, you agree to receive SMS messages from Cleerly recruiters throughout the interview process. Message frequency may vary. Message and data rates may apply. You can STOP messaging by sending STOP and get more help by sending HELP. For more information see our Privacy Policy (https://cleerlyhealth.com/privacy-policy). All official emails will come from @cleerlyhealth.com email accounts.

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