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Quality Engineer

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Onsite

Quality Engineer

EPM Scientific

Quality Engineer

Skills

Compliance

1 month ago

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Important information


Contract type:

Freelance / Contract

Location:

79 Freiburg im Breisgau, Germany

Work mode:

Onsite

Published on:

22 September 2026

What they need


9-12 Month Contract with potential extension

4+ Days On-Site

Baden-Württemberg

We're supporting a leading global medical device organisation looking for an experienced Quality Engineer with a strong focus on Quality Systems to join their team on an initial 9-12 month contract, with a higher potential for extension.

This is a predominantly on-site position, requiring at least 4 days per week on site.

What You'll Do

  • Maintain and continuously improve the Quality Management System (QMS)
  • Manage CAPAs, non-conformances and change controls
  • Lead and support Root Cause Analysis (RCA) and investigations
  • Support internal, external and regulatory audits
  • Review and maintain SOPs and quality documentation
  • Monitor quality metrics and identify continuous improvement opportunities
  • Support document control, training and compliance activities
  • Partner with Quality, Regulatory, Engineering and Operations teams

What We're Looking For

  • A minimum of 2-3 years of quality experience within medical devices or another highly regulated industry
  • Strong knowledge of ISO 13485 and Quality Management Systems
  • Hands-on experience with CAPA, RCA, non-conformances and audits
  • Knowledge of EU MDR, FDA QMSR and/or MDSAP advantageous
  • Strong communication, problem-solving and stakeholder management skills

If you're interested, apply or reach out directly for a confidential conversation and further details.

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