Quality Auditor

An exciting opportunity is available for an experienced Quality Auditor / Quality Specialist to join a Global Development Quality function on a contract basis.This role provides exposure to a broad range of investigational medicinal products, from small molecules through to complex biologics and immunotherapies. You will play a critical role in ensuring the quality, compliance, and release of clinical trial materials, directly supporting the delivery of safe and effective medicines to patients.Key ResponsibilitiesPerform final review of clinical batch records to ensure compliance with GMP requirements and alignment with regulatory submissionsCompile, review, and approve clinical supply data packs for presentation to the Qualified Person (QP) for final releaseConduct routine audits of data, documentation, procedures, systems (including computer systems), equipment, and facilitiesReview and approve production and analytical documentation supporting API, Safety Assessment, and clinical supply lots (bulk and packaged)Ensure compliance with company SOPs, GMP standards, and global regulatory requirementsPerform audits and inspections independently or as part of a teamDocument audit findings, prepare reports, and work with stakeholders to define and implement corrective actionsCommunicate and resolve audit observations with internal teamsEscalate inspection outcomes and quality risks to appropriate managementCollaborate with global clinical supply chain and manufacturing partnersExperience, Knowledge & SkillsExperience within the pharmaceutical industry or a drug regulatory authority, with a solid working knowledge of cGMP regulationsStrong attention to detail and high standards of documentation accuracyExcellent written and verbal communication skillsSelf-motivated with the ability to work confidently with minimal supervisionStrong organisational skills with the ability to manage multiple prioritiesEffective problem-solving and decision-making capabilitiesProficient in Microsoft Office and able to learn GMP-related systems and toolsQualificationsBachelor’s degree in Life Sciences or a related scientific disciplineMinimum of 3 years’ experience in Quality roles within the pharmaceutical industryWe are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

Created: 2026-01-18