Junior Quality Complaint Officer (m/f/d)

Randstad Austria GmbH
Jetzt bewerben

KI-Zusammenfassung

In dieser Rolle sind Sie verantwortlich für den gesamten Lebenszyklus der Bearbeitung von Kundenbeschwerden, von der ersten Annahme bis zur endgültigen Schließung. Sie führen technische Untersuchungen durch und unterstützen die Analyse von Risiken und Trends, um die Produktsicherheit zu gewährleisten. Zudem kommunizieren Sie professionell mit verschiedenen Stakeholdern über den Status der Beschwerden.

Our customer is dedicated to innovation, quality, and safety in medical technology.

Your Responsibilities

In this role, you will take ownership of the end-to-end customer complaint handling lifecycle-from initial receipt through root cause investigation to final closure. You will serve as a vital link in maintaining device safety and driving continuous product improvement.

  • Complaint Management: Receive, review, and log complaints in the complaint handling system, ensuring complete documentation, traceability, and timely resolution.
  • Technical Investigations: Coordinate and perform root cause analyses (using tools like 5-Why, Fishbone/Ishikawa) in close collaboration with R&D, Production, and Regulatory Affairs.
  • Risk & Trend Analysis: Identify quality trends, support Post-Market Surveillance (PMS) activities, and promptly escalate potential safety issues or reportable events to the Quality Assurance Manager.
  • CAPA & Continuous Improvement: Support and recommend CAPA and Non-Conformance (NCR) initiatives resulting from complaint findings, contributing to cross-functional risk management and quality enhancements.
  • Stakeholder Communication: Maintain factual, objective, and professional communication with distributors, service partners, and customers regarding complaint status and updates.

Your Profile

Education & Experience:

  • Education: Technical diploma or a Bachelor's degree in a technical or scientific discipline.
  • Experience: Experience in Quality Assurance, complaint handling, customer quality, technical support, or regulatory affairs-preferably within a regulated manufacturing environment (Medical Devices).
  • Technical Skills: Proven experience in conducting technical root cause investigations and working with complaint management or ERP systems.
  • Regulatory Knowledge: Solid understanding of ISO 13485 and medical device quality management system requirements.

Competencies & Mindset:

  • Language Skills: English proficiency (B1 level minimum, mandatory). Italian (B2 level) is a distinct advantage ("nice to have").
  • Working Style: Strong analytical and problem-solving skills, high attention to detail, and a structured, objective approach to documentation.
  • Personal Traits: Self-starter with strong communication skills, sound professional judgment, customer focus, and a collaborative team-player mindset.

What We Offer

  • A varied, high-impact role within a dynamic medical device environment.
  • The opportunity to actively shape product safety and improve patient quality of life.
  • A supportive, professional team culture with short communication lines.

We are looking forward to your application!

Berufsfeld:

TECHNIK & INGENIEURWESEN

Referenznummer:

JUNIO30224
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