E2E CSV/C&Q Lead

Location: Basel, Switzerland (project scope includes Portsmouth, UK) Start Date: 1 November 2026 Contract Duration: Until 31 October 2027 Lead end\-to\-end computerised system validation and qualification for an innovative manufacturing data pl E2E CSV/C\&Q Lead Job description: We are seeking an experienced E2E CSV/C\&Q Lead to take ownership of the end\-to\-end validation and qualification strategy for a strategic Operations Data Hub (ODH) programme. The position covers integrated manufacturing systems, IT/OT interfaces, infrastructure, semantic data models, data products and operational applications. You will collaborate with Engineering, Automation, Quality, IT/OT and business stakeholders to ensure that solutions meet regulatory, quality and data integrity requirements. Your key responsibilities will include: * Define, implement and maintain an integrated, risk\-based Computerised System Validation (CSV) and Commissioning \& Qualification (C\&Q) strategy. * Establish validation boundaries, intended use, GxP classifications and appropriate controls across the manufacturing data platform. * Develop modular qualification frameworks, documentation standards and reusable validation approaches for future implementations. * Coordinate end\-to\-end validation execution, including requirements traceability, testing, documentation and release readiness. * Define validation approaches for operational applications supporting batch traceability, process monitoring and customer data sharing. * Evaluate data integrity, data lineage, interoperability and auditability across integrated manufacturing systems. * Ensure alignment with ALCOA\+ principles and relevant GMP requirements. * Prepare and coordinate validation documentation for independent Quality review and approval. * Define supplier assurance strategies, including the use of vendor testing and previously qualified components. * Ensure that validated\-state maintenance requirements are incorporated into operational support processes. * Develop qualification templates, implementation prerequisites and resource, cost and timeline estimates for future site rollouts. * Facilitate cross\-functional risk assessments, manage validation dependencies and escalate programme\-level compliance risks. * Support release readiness assessments and coordinate with business and Quality stakeholders throughout implementation. About the customer: Our client is an internationally established organisation within the pharmaceutical and biotechnology sector, specialising in complex, highly regulated manufacturing operations. As part of its digital transformation initiatives, the organisation is implementing advanced manufacturing data solutions to improve connectivity, traceability and operational efficiency across production environments. Requirements: * Bachelor's or Master's degree in Engineering, Automation, Computer Science, IT, Life Sciences, Pharmaceutical Sciences, Quality Management or a related discipline. * Proven experience leading end\-to\-end CSV/C\&Q activities for integrated IT/OT systems, manufacturing data platforms or regulated operational applications. * Strong understanding of GMP, CSV/CSA, Commissioning \& Qualification and risk\-based validation methodologies. * Practical experience managing change control, deviations, CAPA and maintenance of the validated state. * Solid expertise in validation documentation, requirements traceability, testing strategies and supplier assurance. * Strong understanding of data integrity principles, including ALCOA\+. * Knowledge of manufacturing automation environments, MES, historians, system interfaces, infrastructure and data transformations. * Experience collaborating with Quality, Engineering, Automation, IT/OT and external suppliers. * A