GCP Auditor

Nexia; United Kingdom; On-site; GBP 25,000 - 32,000; Full time

Job summary

A biotechnology consulting firm is seeking a skilled GCP Auditor in the United Kingdom. The role involves conducting audits, managing compliance trends, and supporting regulatory inspection readiness. Ideal candidates will have a degree in Life Sciences and experience in GCP auditing. This full-time position offers significant responsibilities in a fast-paced environment and requires excellent communication skills.

Qualifications

• Strong experience in GCP auditing and regulatory compliance.
• Solid understanding of ICH GCP and relevant global regulations.
• Ability to work independently in a remote setting.

Responsibilities

• Conduct GCP audits and prepare clear, concise reports.
• Manage CAPAs through to closure and track compliance trends.
• Support regulatory inspection readiness and participate in inspections.

Skills

GCP auditing

Regulatory compliance

Analytical skills

Communication skills

Organisational skills

Education

Degree in Life Sciences, Quality or related field

Job description

Direct message the job poster from Nexia

Role Overview

We are seeking a skilled GCP Auditor to ensure our clients' clinical trials meet the highest regulatory and quality standards. You will plan, conduct and report on GCP audits across investigator sites, suppliers and internal processes, manage CAPAs, and support inspection readiness activities. This role requires strong GCP knowledge, excellent communication skills and the ability to work independently in a fast-paced environment.

Key Responsibilities

• Conduct GCP audits (site, supplier, internal) and prepare clear, concise reports.
• Manage CAPAs through to closure and track compliance trends.
• Contribute to risk-based audit planning and quality process improvements.
• Support regulatory inspection readiness and participate in inspections.
• Collaborate with cross-functional teams to ensure compliance and best practice.

Requirements

• Degree in Life Sciences, Quality or related field.
• Strong experience in GCP auditing and regulatory compliance.
• Solid understanding of ICH GCP and relevant global regulations.
• Excellent communication, analytical and organisational skills.
• Ability to work independently in a remote setting.

Preferred

• Experience with other GxPs (GCLP, GVP) and global clinical trials.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance, Science, and Research

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

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