QC Validation and Compliance Lead Cheshire £40,000 £50,000 Pharmaceutical / GMP Laboratory The Role We are seeking an experienced QC Validation and Compliance Lead to take ownership of QC laboratory equipment lifecycles and computerized systems within a GMP-regulated environment. This senior, hands-on role blends equipment validation, CSV, data integrity, and team leadership, ensuring QC operations remain compliant, efficient and inspection-ready at all times. Key Responsibilities Own the full lifecycle of QC laboratory equipment, including procurement, qualification, maintenance, change control, and retirement Lead equipment validation activities (IQ/OQ/PQ) and manage site calibration programmes, including oversight of external service providers Manage QC equipment and validation status using electronic systems (e.g. LIMS), ensuring GMP compliance and inspection readiness Lead Computer System Validation (CSV) and administration for QC systems such as Empower and LabX, ensuring data integrity and regulatory compliance Author and approve validation and GMP documentation, and lead deviation investigations, impact assessments, and CAPA related to equipment and systems Provide technical leadership and line management to a small QC systems team and act as SME during internal and regulatory audits What We re Looking For Degree (BSc or equivalent) in Chemistry or a relevant scientific discipline, with essential experience in a pharmaceutical or GMP-regulated laboratory Strong ..... full job details .....