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Quality Auditor

Job in Greater London, London, Greater London, EC1A, England, UK
Listing for: PE Global
Full Time position
Listed on 2026-01-19
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist / Manager, Quality Control / Manager, Quality Technician/ Inspector
Job Description & How to Apply Below
Location: Greater London

PE Global is currently recruiting for a Quality Specialist/Auditor for a leading multi-national Pharma client based in Moorgate, London.

PE Global is currently recruiting for a Quality Specialist/Auditor for a leading multi-national Pharma client based in Moorgate, London.

PE Global is currently recruiting for a Quality Specialist/Auditor for a leading multi-national Pharma client based in Moorgate, London.

PE Global is currently recruiting for a Quality Specialist/Auditor for a leading multi-national Pharma client based in Moorgate, London.

PE Global is currently recruiting for a Quality Specialist/Auditor for a leading multi-national Pharma client based in Moorgate, London.

PE Global is currently recruiting for a Quality Specialist/Auditor for a leading multi-national Pharma client based in Moorgate, London.

PE Global is currently recruiting for a Quality Specialist/Auditor for a leading multi-national Pharma client based in Moorgate, London.

Terms: hybrid work, 37.5 hrs per week, 6 months, £17.79‑£26.51 PAYE, needs UK work visa.

Duties/Responsibilities
  • Final review of clinical batch records to ensure GMP compliance and regulatory filings.
  • Compile and approve data pack and present to QP for release.
  • Conduct routine audits of data, procedures, equipment, systems to meet SOP and GMP standards.
  • Review and approve production and analytical documentation for API, safety assessment, or clinical supply lots.
  • Communicate and resolve audit comments with client areas.
  • Issue reports summarizing deficiencies and work with areas to execute remedial action.
  • Notify appropriate management of inspection result.
Education/Experience
  • Experience in pharmaceutical/chemical industry or government drug‑regulatory agency with cGMP knowledge.
  • Existing QA or similar role in a GMP environment.
  • Effective oral/written communication and interpersonal skills.
  • Confidence to work with minimal supervision and keen eye for detail.

Interested candidates should submit an updated CV.

Please click the link below to apply or send an up‑to‑date CV to

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