Job Title

Principal QA Specialist - UK You'll support the global implementation of quality management systems, ensuring robust documentation processes and effective stakeholder alignment. This role serves as a key liaison between global quality teams and local implementation needs. The role will be working onsite in Slough, starting in May for an initial 12 month contract. Key ResponsibilitiesLead enrolment and site maintenance for global standards processesManage documentation processes and quality recordsSupport implementation of global QMS systems including validation, qualification, and trainingServe as point of contact for new system inquiriesEnsure timely project execution through alignment with global teamsPromote quality culture across the organizationRequired QualificationsBachelor's degree in Science or QA discipline (or equivalent experience)5-10 years' pharmaceutical industry experience in QA rolesAdvanced experience implementing IT PQS systems (particularly Veeva Vault)Documentation management expertiseEssential SkillsExcellent documentation writing capabilitiesStrong communication and collaboration skillsDeep understanding of GMP compliance requirementsProject management expertiseAbility to manage ambiguity and drive resultsDetail-oriented with strong organizational skillsCollaborative team player with stakeholder management abilities