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 Responsibilities Lead enrolment and site maintenance for global standards processes Manage documentation processes and quality records Support implementation of global QMS systems including validation, qualification, and training Serve as point of contact for new system inquiries Ensure timely project execution through alignment with global teams Promote quality culture across the organization Required Qualifications Bachelor's degree in Science or QA discipline (or equivalent experience) 5-10 years' pharmaceutical industry experience in QA roles Advanced experience implementing IT PQS systems (particularly Veeva Vault) Documentation management expertise Essential Skills Excellent documentation writing capabilities Strong communication and collaboration skills Deep understanding of GMP compliance requirements Project management expertise Ability to manage ambiguity and drive results Detail-oriented with strong organizational skills Collaborative team player with stakeholder management abilities