обновлено 2 дня назад
Supplier Quality Engineer (Medical Technology)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Supplier Quality Engineer (Medical Technology): Managing supplier qualification, surveillance, audits, quality records, and corrective actions for outsourced medical technology manufacturing with an accent on supplier quality systems, process validation, and nonconformity prevention. Focus on investigating root causes, implementing improvement plans, coordinating with R&D and regulatory teams, and supporting supplier audits and product registrations.
Location: San Daniele del Friuli, Friuli Venezia-Giulia, Italy
Company
is a medical technology company developing clinically differentiated solutions for orthopedics and other active-lifestyle applications.
What you will do
- Create and maintain Quality Management System procedures, work instructions, quality conditions, and procurement specifications.
- Manage quality records, supplier quality KPIs, nonconformity trends, root cause investigations, and corrective measures.
- Qualify, monitor, and re-evaluate suppliers, including conducting supplier audits when qualified.
- Support suppliers with audit findings, SCARs, product nonconformities, improvement plans, process validation, and initial sampling.
- Collaborate with R&D, Purchasing, Regulatory, Post Marketing Surveillance, Incoming Inspection, and Technical departments.
- Support inspections by Certification and Notified Bodies, Competent Authorities, and other agencies.
Requirements
- Bachelor’s or master’s degree in Engineering, preferably Mechanical, Management, Biomedical, or Bioengineering.
- Previous supplier quality assurance experience in modern manufacturing companies.
- Excellent knowledge of Microsoft Office, particularly Excel.
- Precision, methodical work, multitasking ability, and effective teamwork.
- Written and spoken English at least at B2 level.
- Basic written and spoken German. Willingness to undertake short-term travel within Italy and abroad.
Nice to have
- Lead Auditor qualification accredited by AICQ-CEPAS or AICQ-SICEV.
Culture & Benefits
- Work in an international context with colleagues based in other company offices.
- Collaborate across engineering, manufacturing, purchasing, regulatory, and quality functions.
- Equal employment opportunity and merit-based employment practices.
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