Quality Auditor

Summary

Join Eurofins Healthcare Assurance as a freelance Quality Auditor to conduct GxP and ISO audits in the pharmaceutical, medical device, and cosmetics sectors. You will manage and review pre-audit documentation, prepare audit agendas, collaborate on travel arrangements, execute on-site or remote audits, draft audit reports, revise documents based on client feedback, and evaluate CAPA plans. This role requires proven knowledge of relevant standards (e.g., EU GMP, ISO 9001, ISO 13485), a scientific degree (preferably in Pharmacy, Chemistry, or Pharmaceutical Technologies), and a minimum of 10 completed audits. Fluency in French and flexibility to travel within France are also necessary. Eurofins supports career development and embraces diversity. The company is committed to sustainability and aims for carbon neutrality by 2025.

Requirements

• Self-employed Quality Auditor (freelance status)
• Proven knowledge of relevant standards: EU GMP Part I & II, ISO 9001, ISO 13485, ISO 15378, ISO 22716, 21 CFR Part 210–211, EU GDP, IPEC guidelines
• Scientific degree (preferably in Pharmacy, Chemistry, or Pharmaceutical Technologies)
• Minimum of 10 completed supplier and/or internal audits
• Fluent in French and flexible to travel within France

Responsibilities

• Management and review of pre-audit documentation
• Preparation of audit agendas in coordination with clients
• Collaboration in travel and logistical arrangements
• On-site or remote execution of audits
• Drafting of audit reports and audit findings
• Revising documents based on client feedback
• Evaluation and follow-up of CAPA (Corrective and Preventive Action) plans