About this role
Shape the Future of Pharmaceutical Manufacturing with Tata Chemicals Europe Built on over 100 years of scientific expertise and driven by exceptional people, Tata Chemicals Europe is a business with a proud heritage and an exciting future. Across our Cheshire sites, our colleagues are helping us deliver premium products, outstanding customer service, and a positive impact on our communities and environment. Now, we're entering an exciting new chapter. Be Part of Something Ground-Breaking We've launched Medi-Salt , the UK's first dedicated pharmaceutical-grade salt manufacturing facility. Producing high-purity salt for use as both an Active Pharmaceutical Ingredient (API) and pharmaceutical excipient, Medi-Salt is setting new standards in quality, compliance and innovation. CSV and Data Integrity Manager opportunity has arisen To support our continued growth and commitment to world-class quality, we're looking for a CSV and Data Integrity Manager to be the quality lead for digital, computerised and IT-enabled systems, ensuring that appropriate compliance, data integrity, computer systems validation, information security and audit readiness standards are embedded across the business. The role provides independent quality oversight of computerised systems, data integrity, Computer Systems Validation and information security compliance, ensuring that appropriate methodologies, governance, quality risk management controls, metrics and escalation routes are in place. This is a highly visible role requiring someone who can work autonomously, influence across functions, manage audits and inspections confidently, and apply pragmatic, risk-based judgement while helping teams understand what good looks like without creating unnecessary complexity. Key responsibilities include: Act as the Quality lead for eCompliance, data integrity, Computer Systems Validation and information security compliance across relevant systems and processes. Ensure appropriate methodologies, standards and procedures are developed, maintained and embedded within the Quality Management System. Provide Quality oversight throughout the computer-system lifecycle, including scoping, vendor selection, implementation, validation, go-live, routine operation, change control and periodic review. Ensure systems are compliant, robust, practical to operate and supported by appropriate lifecycle documentation. Ensure data integrity and information security principles are embedded into system design, implementation and operational use. Approve relevant data integrity methodologies, procedures, templates, assessments, remediation plans and change controls for key or critical systems. Review and approve key validation and project lifecycle documentation, including validation plans, GxP assessments, data migration plans, functional risk assessments, UAT/PQ test reports, validation reports, data migration reports and go/no-go decisions where appropriate.