Principal QA Specialist – UK

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

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