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Part‑Time Quality Assurance Site Coordinator

Eurofins · Auckland

Mid 🇬🇧 English
GMP ISO 17025 Quality Management System

Job description

About the role

Eurofins BioPharma Product Testing NZ is seeking an experienced Quality Assurance professional for a part‑time Site Coordinator role. Based in Penrose, Auckland, you will lead the Quality Management System (QMS) and support a culture of compliance and continuous improvement across our GMP‑licensed laboratory.

Key responsibilities

  • Maintain and enhance the site’s QMS to meet GMP, ISO 17025 and other regulatory requirements.
  • Conduct internal audits, document reviews, and corrective actions.
  • Support the Head of Quality AU/NZ and Business Unit Manager in quality‑related decision‑making.
  • Oversee document control, training records, and change management.
  • Drive continuous improvement initiatives and monitor key quality metrics.

Required profile

  • Proven experience in a quality role within a regulated laboratory environment.
  • Strong understanding of GMP, ISO 17025 and quality system documentation.
  • Ability to work flexible part‑time hours within normal business days.
  • Excellent attention to detail and a proactive approach to compliance.

Required skills

  • GMP
  • ISO 17025
  • Quality Management System (QMS)
  • Regulatory compliance
  • Audit techniques

What we offer

  • Flexible part‑time schedule (Monday‑Friday).
  • Opportunity to work in a global leader in life‑science testing.
  • Collaborative environment with professional development support.

Questions fréquentes

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Published 2 months ago

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Eurofins

Auckland