Scientific Search
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 analysis
Revise procedures and maintain document control
Perform quality data analysis and trending
Support audits, risk management, and inspection processes
Collaborate on product and process improvement initiatives
About You
ISO 13485 QMS experience and FDA-regulated industry background
Certified Quality Engineer or Auditor (CQE / CQA) preferred
Strong data analysis and statistical problem-solving skills
Comfortable interfacing across departments and management levels
We are an equal opportunities employer and welcome applications from all qualified candidates.
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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 analysis
Revise procedures and maintain document control
Perform quality data analysis and trending
Support audits, risk management, and inspection processes
Collaborate on product and process improvement initiatives
About You
ISO 13485 QMS experience and FDA-regulated industry background
Certified Quality Engineer or Auditor (CQE / CQA) preferred
Strong data analysis and statistical problem-solving skills
Comfortable interfacing across departments and management levels
We are an equal opportunities employer and welcome applications from all qualified candidates.
#J-18808-Ljbffr