Quality Engineering Supervisor
Pubblicato il 08-10-2026 - Steris in Roma
Overview
In this role you will lead a Quality Engineering team focused on improving process and product quality across multiple production lines. You will manage inspection, NCR investigations, and QC testing while driving Lean and Quality improvements with cross-functional teams. You’ll ensure compliance with ISO 9001, ISO 13485, MDSAP, FDA regulations, and EU MDR, influencing both internal and customer-facing quality metrics. This position offers ownership of team development and data-driven problem solving to reduce nonconformances and drive performance.
Retribuzione / Benefits corporate premio
Responsabilità Lead and develop the Quality team to improve internal production quality metrics (DPU, FPY) and customer-facing quality outcomes
Drive robust data analysis and improvement projects to reduce nonconformances and improve process controls
Align quality improvements with Lean strategies and supplier quality initiatives
Set and manage objectives for individuals and the team in line with the Quality strategy
Support Quality System compliance across ISO 9001, ISO 13485, MDSAP, FDA and EU MDR requirements
Contribute to talent development, training, and performance management of team members
Perform nonconformance investigations and guide problem-solving using established methodologies
Collaborate with CI resources to sustain Lean and quality improvements
Requisiti fondamentali 5-8 years of Quality Engineering experience
5-8 years in healthcare, medical device, or regulated industries preferred
3-5 years in supplier quality
3-5 years in Lean methods
ASQ, QSR, or familiarity with QSR/GMP regulations preferred
3-5 years supervising/leading employees
English language required for communications with non-local teams
Customer focus
Teamwork
Initiative/Leadership
Quality management system
ISO 9001
Lean manufacturing