Sr. Design Quality Engineer

What you’d do

Develop and evaluate medical device designs for manufacturability, reliability, and cost, and create design test methodology to verify performance. Use DMAIC, DRM, Minitab, and statistical methods such as DOE, SPC, and ANOVA while following FDA design and manufacturing requirements. Full time. Found on the employer's careers page on Oct 18, 2026. Apply through the link.

You’ll need

• Master's in mechanical, industrial, or biomedical engineering or related field
• 2 years as a quality, product, or validation engineer
• 2+ years with DMAIC and DRM methodologies
• 2+ years with Minitab and statistical methods (DOE, SPC, ANOVA)
• Knowledge of FDA medical device design and manufacturing requirements