Senior Quality Specialist (w/m/d)

GE HealthCare UK

Zipf, Austria
Base: €65,000 + annually; bonus/equity: not specif...
On-site
Design transfer and production introduction
Quality and compliance requirements
International quality management systems
The Senior Quality Specialist position at GE HealthCare in Zipf, Austria, focuses on ensuring quality and compliance in product lifecycle management, particularly in design transfer and manufacturing projects. The role requires significant experience in quality management within regulated environments, preferably in medical technology, and offers a competitive salary and flexible working conditions

Job Summary

  • As a Senior Quality Specialist, you will play a central role in design and production transfer projects, ensuring regulatory compliance and actively contributing to the development of our quality culture.
  • You will be responsible for quality assurance across the entire product lifecycle, with a particular focus on design transfer and production introduction.
  • GE HealthCare offers a role with a broad spectrum of tasks in a growth-oriented company, an interdisciplinary team, and a competitive salary starting from €65,000 annually.

Matching Summary

Match Score: 85

The Senior Quality Specialist position at GE HealthCare in Zipf, Austria, focuses on ensuring quality and compliance in product lifecycle management, particularly in design transfer and manufacturing projects. The role requires significant experience in quality management within regulated environments, preferably in medical technology, and offers a competitive salary and flexible working conditions.

Salary

Base: €65,000+ annually; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Design Transfer and Production Introduction
  • Quality and Compliance Requirements
  • International Quality Management Systems
  • Manufacturing and Production Transfer Projects
  • Cross-functional Project Leadership

Nice-to-have

  • AI-related development processes
  • Quality culture development
  • Continuous improvement methods

Key Requirements

  • Degree in Quality Management, Engineering, or similar
  • Several years of experience in regulated environments
  • Experience in Medical Technology/Medical Devices
  • Knowledge of ISO 13485, MDR, FDA 21 CFR
  • Experience in Manufacturing, Design Transfer
  • Excellent Project Management skills
  • Fluent German, English B2 minimum

Work Rights

Not specified

Tailored Resume

Cover Letter