CSV Auditor

At Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each person is not only valued but empowered to thrive and make a meaningful impact.

Company Culture

Our people–both employees and consultants—are the heart of Advarra. They are the key to our success and the driving force behind our mission and vision. Our values (Patient-Centric, Ethical, Quality Focused, Collaborative) guide our actions and decisions. Knowing the impact of our work on trial participants and patients, we act with urgency and purpose to advance clinical research so that people can live happier, healthier lives.

Job Overview Summary

Advarra is seeking CSV Auditors to join our consultant network for EU-based projects. Auditors ensure compliance with GxP regulations and provide expertise across clinical, laboratory, and manufacturing systems.

Job Duties & Responsibilities

• Conduct Computer System Validation (CSV) audits for life science clients.
• Assess compliance with GxP regulations and client requirements.
• Develop audit reports and provide recommendations.
• Collaborate with client teams to ensure remediation actions are implemented.

Location

This evergreen role is open to candidates based in the EU region.

Basic Qualifications

• Minimum ten (10) years of Quality Assurance and/or GxP experience in life sciences.
• Minimum five (5) years of Quality Assurance auditing experience.
• Strong interpersonal and client interaction skills.
• Excellent verbal and written communication in English.