Quality Engineer

What you’d do

Quality engineer supporting product, process, and quality system performance in a regulated medical device manufacturing environment. Owns QMS processes including document change control, calibration, CAPA/root cause investigations, and supplier quality, and partners with production, engineering, and supply chain to reduce defects. Full time. Found on the employer's careers page on Oct 18, 2026. Apply through the link.

You’ll need

• Experience in medical device manufacturing
• Knowledge of ISO 13485, FDA QSR (21 CFR 820), ISO 14971
• SPC, Cpk/Ppk, MSA/Gauge R&R, PFMEA/DFMEA
• Process validation (IQ/OQ/PQ)
• Supplier qualification and SCARs