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QE Engineer

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Hybrid

QE Engineer

Randstad Technologies Italia

QE Engineer

Skills

Data AnalysisComplianceRegulatory CompliancePower BI

24 days ago

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Important information


Contract type:

Permanent

Salary:

€38,000 – €46,000 / year

Location:

00071 Pomezia, Metropolitan City of Rome Capital, Italy

Work mode:

Hybrid

Published on:

29 September 2026

What they need


Randstad Digital Talent Services, a specialized division of Randstad dedicated to recruiting high-caliber IT and technology professionals, is partnering with a global leader in medical devices and healthcare services to hire a Quality Engineering Supervisor .

Role Overview

Reporting directly to the Quality Manager, the Quality Engineering Supervisor will lead a cross-functional team of Quality Engineers, Technicians, and Inspectors. This role bridges core operational and regulatory compliance (GMP, ISO 13485, ISO 9001, FDA 21 CFR Part 820/211, EU MDR) with digital quality initiatives, including MES/eQMS integration, Non-Conformance Resolution (NCR), CAPA management, and Business Intelligence-driven KPI analytics.

Key Responsibilities

  • Direct and mentor a multidisciplinary team (Quality Engineers, Technicians, Inspectors, and Data Quality Analysts), setting performance goals, managing workloads, and driving professional development
  • Track internal and customer-facing quality metrics (DPU - Defects Per Unit, FPY- First Pass Yield) using BI dashboards and advanced data analytics
  • Oversee non-conformities (NCR) through eQMS platforms, leading Root Cause Analysis (RCA) and corrective/preventive action plans
  • Supervise incoming inspection and final QC testing activities integrated with plant manufacturing execution systems (MES)
  • Digitalization & Continuous Improvement: Drive the transition toward Industry 4.0 in close partnership with Continuous Improvement and Lean teams
  • Align manufacturing quality standards with broader Supplier Quality strategies and monitor vendor performance
  • Ensure full Quality Management System (QMS) compliance with cGMP regulatory standards (ISO 13485, ISO 9001, MDSAP, FDA 21 CFR Part 820/211, EU MDR)

Requirements & Qualifications

  • Bachelor's or Master's degree in Engineering (required)
  • At least 5 years of experience in Quality Engineering within highly regulated industries (Medical Devices, SaMD, Healthcare, Pharma, or advanced manufacturing)
  • At least 3 years of experience managing and leading teams
  • 3+ years of hands-on experience applying Lean methodologies, Supplier Quality frameworks, and problem-solving tools (FMEA, SPC, RCA)
  • Technical & Digital Skills: Proficiency in eQMS software, MES platforms, and BI/data analytics tools (Excel, Minitab, Power BI, Visio)
  • Language: Professional working proficiency in English (written and spoken)

Compensation & Benefits

  • Location: Pomezia (Rome, Italy) with a hybrid work model
  • Employment Type: Full-time, permanent position
  • Salary Range: 38K€ – 46K€ (commensurate with experience)
  • Benefits: Corporate welfare package, employee perks, and ongoing professional development opportunities

"This announcement is open to candidates of all genders (pursuant to Italian Law 903/77 and 125/91) and individuals of all ages and

nationalities (Legislative Decree 215/03 and 216/03). Please submit your resume with authorization for the processing of personal data (GDPR EU 2016/679)."

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