Senior Verification & Validation Engineer at Sibel Health

A BIT ABOUT SIBEL HEALTH:

With headquarters based in Chicago, Illinois and an international office in Seoul, South Korea, Sibel Health is an award-winning digital health startup with a mission to deliver Better Health Data for All®. We were founded with a specific focus on our most vulnerable patients—pregnant persons and babies—where we believe wireless monitoring has the potential to do the most good worldwide. We achieve this by providing a complete monitoring solution of advanced wireless wearables, best in class software, and novel AI/ML algorithms all linked to the cloud. To date, we’ve launched our technologies in 20 countries from the most advanced hospitals in the world to the most resource constrained locations. We work with some of the most respected healthcare organizations in the world from major philanthropies to large medical technology and pharmaceutical companies. With numerous FDA clearances and a recently completed fundraising round, we are poised for growth and expansion. We are seeking mission-driven individuals with a strong sense of purpose who believe that technology can improve the lives of our most vulnerable patients.

THE OPPORTUNITY: 

We are seeking a Senior Verification & Validation Engineer to support product verification and validation planning and execution for products in our Discovery and Clinical portfolio, including wearable sensors and medical monitoring system solutions. You will be responsible for reviewing requirements to ensure clear and testable requirements, defining V&V test strategy, and creating and managing verification test plans, protocols, and reports. You will be a critical member of a cross-functional team in pursuit of delivering innovative and quality products that adhere to our technical designs and meet the needs of our customers. We value candidates who have a strong work ethic, are detail-oriented, and are passionate about improving product quality and usability through user-centered V&V testing. This is a great opportunity to join a diverse, innovative, and passionate team that shares a common vision to provide Better Health Data for All®.

This is a full-time position. The salary range for this role is $105,000 - $135,000, depending on level of experience.

WHAT YOU WILL BE WORKING ON: 

• Planning and managing the verification activities for multiple projects, coordinating with project management on verification timelines, deliverables, and readiness.
• Experience reviewing and examining requirements, interface specifications, UI/ID specifications, and technical design documents. 
• Ability to translate requirements and design documents into verification protocols, taking into account both technical design and clinical use cases.
• Defining and implementing test strategies and methodologies for multiple projects. 
• Performing manual and automated testing and analysis to identify and document any anomalies. 
• Developing and maintaining automated test scripts using appropriate tools and languages (e.g., Python, C++, test frameworks).
• Maintaining accurate and complete documentation of all verification activities, including verification plans, verification reports, and anomalies reports. 
• Responsible for overseeing the various validation activities, working closely with Product Management, to ensure they are completed in accordance with the V&V Plan. 
• Pro-actively collaborating with other groups including Systems Engineering, UI Designers, Product Management, and the Engineering teams (SW, HW, FW, Algorithm).
• Working within an Agile team environment, supporting in-sprint verification activities and planning.

ABOUT YOU: 

• Bachelor's degree in engineering, computer science, or a related technical field. 
• 5+ years experience in verification/V&V/tester/automation engineering or similar role.
• Experience in regulated industry, medical device industry is preferred.
• Knowledge in system-level design, requirements management, and V&V processes and tools.
• Solid understanding of medical device regulations and standards (e.g., FDA QSR, ISO 13485, IEC 60601).
• Experience in automation tools and platforms is preferred. 
• Strong problem solving skills, detail oriented, with a passion to drive product quality through user-centered testing.
• Self-motivated and can effectively adapt and prioritize multiple projects/tasks while meeting expected deadlines.
• Must be a resident or be willing to relocate to Chicago, IL. 

BENEFITS:

• Medical, dental, vision, life, and disability insurance.
• "Take as much time as you need" policy.
• Simple IRA plan with employer matching.
• Company sponsored events and lunches.
• Yearly stipend for professional development.
• Opportunity to be part of a dedicated and driven team that is here to disrupt and revolutionize wireless monitoring.

Sibel Health Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.