Product Quality Engineer (w/m/d)

BAXTER HEALTHCARE PTY AUS

Saalfeld, Germany
Not specified; competitive compensation mentioned
Onsite
Medical device quality documentation
Fmea risk analysis experience
Design history file management
The role involves creating and maintaining quality documentation such as Design History Files within the product development process

Job Summary

  • The role involves creating and maintaining quality documentation such as Design History Files within the product development process.
  • Candidates must possess strong skills in risk analysis, FMEA activities, and the validation of product changes for medical devices.
  • Baxter offers flexible working models, professional development programs, and a culture focused on saving and sustaining lives.

Matching Summary

The role involves creating and maintaining quality documentation such as Design History Files within the product development process.

Salary

Not specified; Competitive compensation mentioned

Skills & Requirements

Must-have

  • Medical device quality documentation
  • FMEA risk analysis experience
  • Design History File management
  • Product testing and validation planning
  • German and English language proficiency

Nice-to-have

  • PDCA and 8D methodology knowledge
  • Collaborative team environment
  • Structured presentation of analysis results
  • Experience with supplier quality issues

Key Requirements

  • Technical or biomedical engineering degree
  • Multi-year experience in medical device quality
  • Fluency in German and English required

Work Rights

Not specified

Tailored Resume

Cover Letter