Quality Auditor

JR United Kingdom; City Of London; Hybrid; GBP 30,000 - 45,000; Full time

Job summary

A global pharmaceutical company in London seeks a Quality Auditor for a 6-month hybrid role. The successful candidate will conduct audits to ensure compliance with SOPs and regulatory standards, impacting both human and animal health. Ideal candidates will have a scientific background and experience in a GMP-compliant environment.

Qualifications

• Degree qualified in a science-related field.
• Prior experience in the pharmaceutical or chemical industry.
• Proven ability to conduct audits or inspections.

Responsibilities

• Conduct routine audits of data, procedures, and systems for compliance.
• Review and approve production and analytical documentation.
• Collaborate with operational teams on corrective actions.

Skills

Knowledge of cGMP regulations

Auditing

Attention to detail

Education

Bachelor’s degree in a science-related field

Job description

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Quality Auditor, london (city of london)

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Client:

S3 Science Recruitment

Location:

london (city of london), United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

3

Posted:

16.06.2025

Expiry Date:

31.07.2025

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Job Description:

We are on the lookout for a Quality Auditor to join our client based in London – a global pharmaceutical company committed to advancing both animal and human health. In this role, you’ll support compliance by conducting audits across systems, data, procedures, equipment, and facilities to ensure alignment with SOPs, GMP, and international regulations. You’ll also review and approve production and analytical documentation for the release of clinical and safety assessment batches, identify and resolve audit findings, and collaborate with teams to implement corrective actions.

This is a hybrid role offered on a 6-month contract basis.

Key responsibilities:

• Conduct routine audits of data, procedures, equipment, systems (including computer systems), and facilities to ensure compliance with SOPs, GMP, and global regulatory standards
• Review and approve production and analytical documentation related to the release of API, Safety Assessment, and clinical supply lots (bulk and packaged)
• Assess conformance of documentation and processes to regulatory requirements and internal quality standards
• Perform audits or inspections of assigned areas or systems independently or as part of a team
• Identify, document, and communicate audit findings, ensuring timely resolution with relevant departments
• Issue audit reports summarising observations, deficiencies, and required corrective actions
• Collaborate with operational teams to implement and verify effectiveness of remedial actions
• Escalate significant findings and inspection outcomes to appropriate management for review and follow-up

Job requirements:

• Prior experience in the pharmaceutical or chemical industry or with a government drug-regulatory agency, ideally within a GMP-compliant environment
• Knowledge of cGMP regulations
• Previous experience with QA or similar GMP environment
• Proven ability to conduct audits or inspections of systems, facilities, procedures, and documentation for compliance
• Comfortable working independently or as part of a team, with moderate supervision
• Degree qualified in a science-related field (Bachelor’s degree minimum); open to science graduates with a willingness to learn