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Be ready to walk through how you design test plans, log defects, and prioritize regression vs. usability feedback. Use O*NET-style examples: database impacts, negative tests, and clear developer recommendations.
Strong fit if you enjoy structured defect analysis, standards-driven test documentation, and senior-level guidance for software quality in a medical-devices setting. Role is on-site in Wilmington (not remote).
As a Senior Quality Engineer at Elevaris Medical Devices in Wilmington, a typical day centers on finding and documenting defects, designing test plans and scripts, and feeding clear usability and functionality notes back to developers. Expect regression, negative, and retest work plus tracking issues in a bug system so medical-device software stays compliant and reproducible.
Build testing depth with free resources:
No. The listing is for Wilmington, New Hanover County, with remote set to off-site/on-site work.
Core tasks include analyzing failures, logging bugs, writing test plans and procedures, and advising developers on usability and function.
Use free paths such as freeCodeCamp, Saylor CS courses, CS50 (free to learn), and Microsoft Learn developer training.
Public-domain labor data — prepare examples for 2–3 of these.
Senior Quality Engineer at Elevaris Medical Devices in Wilmington, New Hanover County About the Role The desired candidate will have prior experience as a Senior Quality Engineer, preferably working in a medical device company. Specific responsibilities include maintaining the supplier quality program (agreements, performance etc.), supporting Customer Complaints; performing failure investigations; supporting Non-Conforming Material; and managing compliance with regulatory requirements. What You'll Do Maintain the supplier quality program including agreements, performance monitoring, and corrective actions. Support customer complaints by investigating issues, analyzing root causes, and implementing corrective measures. Perform failure investigations to identify defects and their sources in products or processes. Manage non-conforming material to ensure compliance with regulatory standards. Ensure adherence to all relevant quality management systems and regulations. Skills & Qualifications Minimum 5 years of experience as a Senior Quality Engineer, preferably in the medical device industry. Demonstrated ability to manage supplier relationships and quality programs. Experience with failure analysis and root cause investigation techniques. Strong understanding of regulatory requirements for medical devices. Able to work independently while maintaining a team-oriented approach. More About Elevaris Medical Devices Elevate your career in the medical device industry with Elevaris Medical Devices. Located in Wilmington, New Hanover County, we are dedicated to improving patient outcomes through innovative and reliable medical solutions. Our commitment to quality is reflected in every aspect of our operations. How to Apply To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there. We look forward to hearing from you!
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