Summary: A biopharmaceutical company in Waterford requires a LIMS Site Implementation Lead to support the implementation of a new site-wide LIMS. The successful candidate will be responsible for coordinating configuration, stakeholder engagement, and phased deployment to support quality control, laboratory operations, and data integrity across the site. Responsibilities: Conduct gap analysis and pre-scoping workshops to identify system configuration requirements. Support the deployment of a core Laboratory Information Management System (LIMS) model at site level. Enable and manage LIMS functionalities including: QC instrument management, QC reagent management, QC sample management, raw material management, finished product management and stability testing management. Activate and coordinate interfaces with partner or enterprise systems (for example ERP platforms). Ensure capability for laboratory instrument connectivity and data integration is established and maintained. Performing diagnostic & analysis of current performance. Delivering relevant business case for implementation. Simplifying business process with SME before deploying the Digital solution. Implementing E2E the selected Smart Factory solutions through defined gates with team coordination, budget and planning management. Managing change management and communication plan. Setting the site Community of Practices and proposing improvement features to Global Product owners, then transitioning to Business System Owner. Performance diagnostic on the relevant scope. Site road map execution for the related solution. Global Site Digital road map. Global Site performance plan. Value realization of the Digital solution. Qualifications & Experience: Bachelors degree (or higher) in Life Sciences, Chemistry, Biochemistry, Engineering, or a related scientific or technical discipline. Minimum 8+ years of relevant experience within a pharmaceutical or biopharmaceutical manufacturing environment. Strong QC laboratory background, with hands-on experience in laboratory processes, testing workflows, documentation practices, and compliance within GMP-regulated environments. Proven experience working with and/or implementing Laboratory Information Management Systems (LIMS), including configuration, user support, and system integration with laboratory instruments or enterprise systems. Demonstrated project management experience, coordinating cross-functional teams, timelines, and deliverables in complex site or digital transformation projects. Solid understanding of GMP, data integrity, and regulatory requirements impacting laboratory and manufacturing operations. Excellent communication, stakeholder engagement, and organisational skills, with the ability to work effectively across technical, quality, and operational teams. SMS certified would be desired. Good understanding of data management and IA digital products.