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