Hobson Associates
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.
What You’ll Do
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
What You Bring
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".
#J-18808-Ljbffr
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.
What You’ll Do
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
What You Bring
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".
#J-18808-Ljbffr