Quality Auditor (Life Sciences)

TL;DR

Quality Auditor (Life Sciences): Conducting GxP audits for pharmaceutical providers to ensure compliance with international regulations with an accent on audit reporting and CAPA assessment. Focus on validating customer audit requests, performing on-site and remote inspections, and mitigating supply chain risks.

Location: Anywhere in Germany. Relocation to Germany is possible.

Salary: 50k – 70k €

Company

A leading supply chain compliance management company in the Life Sciences industry serving over 1,500 pharmaceutical companies globally.

What you will do

• Prepare and conduct approximately 40 remote and on-site GxP audits per year.
• Assess pharmaceutical providers against international GMP regulations and guidelines.
• Create accurate audit reports and collaborate with cross-functional teams for review.
• Review supplier CAPA responses to ensure findings are appropriately addressed.
• Manage the audit lifecycle by negotiating dates and communicating with stakeholders.
• Support continuous improvement initiatives for auditing methodologies and quality processes.

Requirements

• Bachelor’s or Master’s degree in Pharmacy, Chemistry, Biotech, or Life Sciences.
• Minimum 5 years of GMP auditing experience in the pharmaceutical industry.
• Accredited auditor training or equivalent justified experience.
• Strong knowledge of international GMP regulations and quality systems.
• Professional proficiency in English and Spanish.
• Willingness to travel for domestic and international on-site audits.

Nice to have

• Proficiency in French, Italian, or German.

Culture & Benefits

• Hybrid work model, including the possibility to work from anywhere for up to 3 months per year.
• Competitive compensation package with annual reviews.
• Country-specific benefits including private health care, fitness, and meal allowances.
• Annual personal development budget.
• Annual all-company celebration event in Europe.
• Provision of high-quality equipment and tools.