Quality Engineer

Are you a hands‑on Quality Engineer who lives and breathes GD&T and has PC‑DMIS CMM programming experience? Then this could be your next career step.

Join a well‑established contract manufacturer with eight U.S. locations and ~900 employees, supporting highly regulated customers across medical device, aerospace, and automotive markets. This is a visible role where quality engineering directly impacts product performance and compliance.

• Lead quality engineering activities across multiple programs
• Own IQ/OQ/PQ validations, test protocol development, and execution
• Drive CAPA, non‑conformances, root cause analysis, and risk management
• Develop PFMEAs, inspection plans, and technical documentation
• Program CMMs using PC‑DMIS to support GD&T‑driven inspection
• Ensure compliance with FDA 21 CFR Part 820, ISO 13485, and AS9100
• Support internal and external audits
• Collaborate with Engineering, Manufacturing, Supply Chain, and Regulatory teams

• Advanced GD&T expertise (certification strongly preferred)
• Hands‑on CMM programming experience required (PC‑DMIS)
• Experience with metrology/inspection tools (CMMs, Keyence IM, etc.)
• Strong Quality Engineering fundamentals (CAPA, PFMEA, audits, test protocols, QMS)
• 3–5+ years of Quality or Validation experience in a regulated manufacturing environment
• BS in Engineering or related field (AS considered with additional experience)
• Working knowledge of statistical tools (Excel, Minitab)
• Quality certifications (CQE, CQA, Six Sigma, ISO 13485) are a plus

If your background is rooted in GD&T‑driven inspection and PC‑DMIS programming, this role offers the chance to work on complex, regulated products with a stable and growing manufacturer.

Interested? Click "Apply Now".