Quality Engineering S

The Quality Engineer, IVD Quality supports the implementation, maintenance, and execution of supplier-quality and post-market Quality processes for GeneDx’s IVD and software-enabled IVD products. The role reports to the Director, IVD Regulatory and Quality and works in close partnership with senior members of the IVD Quality team.

This hands‑on role is initially focused on supplier quality, including supplier qualification, monitoring, change management, performance monitoring, and supplier‑related investigations. The role also executes assigned post‑market Quality activities, including complaint handling, nonconformance and deviation management, CAPA support, investigations, and Quality trend reporting.

Support implementation, maintenance, and continuous improvement of established IVD supplier‑quality and post‑market quality processes.

Partner with Procurement and other applicable stakeholders to support supplier onboarding, risk classification, qualification, change management, monitoring, and performance management; maintain supplier qualification records, Quality Agreements, and the Approved Supplier List.

Evaluate supplier‑initiated changes and quality events for potential impact on product quality, supply continuity, or regulatory status; elevate complex or high‑risk assessments as appropriate.

Execute assigned post‑market quality activities, including complaint intake and investigation support, nonconformances, deviations, CAPAs, quality‑event documentation, action tracking, and effectiveness checks.

Investigate supplier‑related quality events and assess whether supplier materials, reagents, software, services, or performance may have contributed to a complaint, deviation, nonconformance, or other post‑market event.

Compile supplier and post‑market quality metrics and support trend reporting, management review, and quality‑governance activities.

Draft and maintain supplier‑quality and post‑market quality procedures, work instructions, forms, templates, and quality records, following established QMS standards.

Support audit and inspection readiness by organizing objective evidence and responding to requests under the direction of Quality leadership.

Identify process gaps and improvement opportunities within assigned processes and elevate recommendations for broader QMS changes.

Bachelor’s degree in a scientific, engineering, technical, or related discipline.

Minimum of 3 years of Quality Engineering, Quality Assurance, supplier quality, or related experience, including at least 2 years within an IVD, molecular diagnostics, medical‑device, or similarly regulated environment.

Experience with supplier qualification, supplier monitoring, quality agreements, supplier corrective actions, supplier change assessments, and supplier performance monitoring.

Experience supporting at least one post‑market quality process, such as complaint handling, nonconformance management, deviation management, CAPA, investigations, or quality trending.

Working knowledge of applicable FDA quality‑system requirements, ISO 13485, and ISO 14971.

Ability to execute defined quality processes, manage multiple priorities, and elevate issues appropriately.

Certificates, Licenses, Registrations

ASQ Certified Quality Auditor (CQA), ASQ Certified Quality Engineer (CQE), ISO 13485 Internal Auditor, and/or ISO 13485 Lead Auditor certification preferred.

This is a fully remote position. The employee will work from a home office or other suitable remote location with reliable high‑speed internet access. Work is performed in a climate‑controlled environment using standard office equipment including computer, phone, and video conferencing tools. Standard work hours are Monday through Friday, 9 AM to 5 PM EST.

Ability to travel up to 20% of the time, including occasional domestic and international travel, to conduct supplier audits and support supplier qualification activities.

At GeneDx, we're driven by urgency and purpose: helping patients get diagnosed earlier. We step up, take initiative, and deliver on our commitments - with quality, speed, and care.

Grow fast (be curious, speak up, be agile) We stay curious, ask questions, and share direct feedback with respect. We provide competitive compensation and benefits that reflect local market practices and legal requirements in each country where we operate, helping employees thrive both professionally and personally.

All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability, age, and other characteristics protected by law.

All privacy policy information can be found here .

GeneDx uses AI to aid in our hiring process, where Greenhouse’s Talent Match (“GTM”) feature is used to review applications.