Engineering

Interim Quality Consultant

  • Location

    Reutlingen

  • Sector:

    Medical Devices

  • Job type:

    Contract

  • Salary:

    €100 - €120 per day

  • Contact:

    Max Jones

  • Contact email:

    m.jones@ioassociates.eu

  • Job ref:

    BBBH163280_1752245856

Interim Quality & Regulatory Consultant - MedTech (Freelance)

South Germany | Full-time | Freelance / Interim | Medical Devices

We're looking for an experienced Quality & Regulatory Consultant to support a leading MedTech company with QMS remediation and CAPA system improvements during a key regulatory transition phase.


Your Role

  • Support QMS remediation aligned with EU MDR, ISO 13485, and GxP
  • Help optimize CAPA and NC management systems
  • Contribute to audit readiness and inspection preparation
  • Collaborate with internal teams and suppliers on quality and compliance topics
  • Provide input on risk management and regulatory documentation

Your Profile

  • 5+ years in Quality Management or Regulatory Affairs in MedTech or Life Sciences
  • Familiar with QMS transitions, CAPA systems, and audit processes
  • Knowledge of ISO 13485, ISO 14971, EU MDR, and GMP/GxP
  • Strong communication skills in German and English
  • Hands-on, solution-oriented, and comfortable working independently

What We Offer

  • A meaningful role in a high-impact project
  • Flexible freelance engagement with autonomy and influence
  • Opportunity to work with a forward-thinking MedTech team

Interested?


Send your CV or project portfolio to or apply below