CSV and Data Integrity Manager

Overview

Location: Natrium House - Northwich, Cheshire

Final date to receive applications: 21 August 2026

Department: Quality

Compensation: £55,000 - £65,000 / year

Description: 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.

We are entering an exciting new chapter.

Be Part of Something Ground-Breaking: We have 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 To support our continued growth and commitment to world-class quality, we are looking for a CSV and Data Integrity Manager to be the quality lead for digital, computerised and IT-enabled systems, ensuring 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.

• 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.

• Degree or equivalent in a scientific, technical, quality, compliance, IT, systems or business-related discipline, or equivalent practical experience overseeing computerised systems in a regulated or compliance-led environment.
• Experience in GxP, ERES, pharmaceutical, chemical, manufacturing, life sciences or another highly regulated environment.
• Experience of Computer Systems Validation, system lifecycle documentation, change control and periodic review in a regulated or compliance-led environment.
• Experience of managing or supporting regulatory inspections, customer audits or formal compliance audits. Strong understanding of data integrity expectations and how these apply to computerised systems and operational processes.
• High level of technical ability, able to understand system architecture, access controls, data flows, back-up arrangements, resilience requirements and system-change implications.
• Strong stakeholder-management skills, with the confidence to influence across Quality, IT and operational teams.
• Strong written and verbal communication skills, including the ability to prepare audit material, policies, reports and senior-management updates.
• Pragmatic and solutions-focused, with the ability to balance compliance requirements with operational practicality.
• Formal training or qualification in auditing, validation, Quality Management, Computer Systems Validation, GxP, IT governance, data integrity or information security would be beneficial.

• 37 days holidays per year, inclusive of Bank Holidays
• Roll over of up to 5 days and salary sacrifice holiday purchase scheme
• An additional paid day off each year to volunteer for a good cause in the local community
• 37.5 hours per week, Monday to Friday
• Excellent contributory Pension scheme up to 9% company contribution
• Life insurance
• Private Healthcare