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