Senior QA Validation Specialist Location: Windsor, UK Contract: 6‑month Fixed-Term Contract Industry: Pharmaceuticals About the Role We are currently seeking an experienced Senior QA Validation Specialist to join a pharmaceutical site in Windsor on a 6‑month contract. This role will act as the QA lead for the CQV (Commissioning, Qualification & Validation) department, providing quality oversight and ensuring all validation activities are performed in compliance with GMP and regulatory expectations. This is a senior, site-facing position requiring strong validation knowledge, confident stakeholder interaction, and hands-on QA experience within a regulated pharmaceutical environment. Key Responsibilities * Act as the primary QA representative for the CQV function * Provide QA oversight for commissioning, qualification, and validation activities * Review and approve validation documentation including VMPs, protocols, reports, risk assessments, and SOPs * Ensure CQV activities comply with GMP, regulatory requirements, and internal quality systems * Support deviations, change controls, CAPAs, and quality risk assessments related to validation * Partner closely with Engineering, CQV, Manufacturing, and QC teams on site * Support audit and inspection readiness related to validation activities Skills & Experience Required * Significant experience in QA within a pharmaceutical environm...