The Role:
We’re looking for a Quality Engineer to take ownership of CAPA, quality investigations, and non-conforming material processes in a regulated medical device environment. This is a hands-on role where you’ll drive root cause analysis, implement meaningful improvements, and influence product quality across the lifecycle—not just on the manufacturing floor.
What You'll Do:

+ Own CAPA processes from initiation through closure, including root cause analysis and effectiveness checks

+ Lead quality investigations and resolve non-conforming material (NCMRs)

+ Identify gaps in quality systems and implement sustainable improvements

+ Partner with Engineering, Regulatory, and Operations to resolve issues quickly and effectively

+ Support Design Quality activities to ensure quality is built into products early

+ Analyze data, document findings, and drive decisions using structured problem-solving methods

What You Bring:<...