Quality Engineer Supervisor
Pubblicato il 04-10-2026 - Steris in Italia
Overview You will lead a Quality Engineering team to improve process and product quality across production lines, driving key quality metrics and regulatory compliance. You will manage NCR investigations, inspections, and customer-facing quality performance while partnering with Lean/CI resources to sustain improvements. The role emphasizes developing talent, implementing data-driven problem solving, and aligning quality initiatives with supplier and manufacturing strategies. This is a mission-driven role focused on delivering robust quality control in a regulated environment.
Retribuzione / Benefits
~ corporate premio
Lead the quality team to improve internal production quality and customer-facing metrics
Drive data analysis and improvement projects to reduce defects and improve FPY and DPU
Ensure robust process controls aligned with Lean and production strategies
Coordinate with supplier quality and implement supplier improvement actions
Contribute to Quality System compliance with ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR
Manage inspection activities for incoming product/components and final QC testing
Analyze quality performance data and escalate issues as needed
5-8 years of Quality Engineering experience
~5-8 years in healthcare, medical device or regulated industry preferred
~3-5 years in supplier quality
~3-5 years in Lean methods
~ ASQ, QSR, or familiarity with QSR/GMP regulations preferred
~Customer-focused mindset
~ Teamwork and collaboration
~ Quality Management System knowledge (QMS)
~ QSR/GMP regulations familiarity
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