Quality Engineer
Location : Newport News, VA (onsite, 5 days / week)
Step into a critical role at the intersection of quality and innovation. As a Quality Engineer, you'll be embedded in an FDA-regulated, ISO 13485-certified environment where your expertise will drive product excellence and regulatory compliance. Join a team that values precision, collaboration, and continuous improvement.
Why You Should Apply
- Work onsite in a dynamic, highly regulated medical device environment
- Lead investigations for NCRs, SCARs, and CAPAs
- Collaborate across QA, R&D, and Engineering teams
- Drive ISO 13485 compliance and document control systems
What You'll Be Doing
Investigate nonconformities, manage complaints, and lead root cause analysisRevise procedures and maintain document controlPerform quality data analysis and trendingSupport audits, risk management, and inspection processesCollaborate on product and process improvement initiativesAbout You
ISO 13485 QMS experience and FDA-regulated industry backgroundCertified Quality Engineer or Auditor (CQE / CQA) preferredStrong data analysis and statistical problem-solving skillsComfortable interfacing across departments and management levelsWe are an equal opportunities employer and welcome applications from all qualified candidates.
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