The LabWare LIMS Administrator will be responsible for the day-to-day administration, maintenance, and continuous improvement of the LabWare LIMS system across the site. This role supports both local and global LIMS operations, ensuring data integrity, regulatory compliance, and efficient system performance. The successful candidate will lead system enhancements, support software qualification activities, and provide technical guidance to users and cross-functional teams.Key ResponsibilitiesLIMS Administration & System ManagementPerform functional administrator duties for the LabWare LIMS system, including static data management and change management.Execute routine administrative tasks such as user access management, periodic audit trail reviews, and ongoing system monitoring.Initiate, manage, and implement LIMS-related change controls in compliance with Quality Systems (QS) requirements.Troubleshooting & SupportProvide technical support for day-to-day system issues from investigation through resolution, including both local and global LIMS incidents.Collaborate with global LIMS administration and IT infrastructure teams to ensure global processes and system performance are maintained.System Enhancements & ValidationDevelop and implement new functionality and system enhancements within LabWare LIMS.Lead system enhancement and improvement projects, including static data builds, Computer System Validation (CSV) activities, and end-user training.Act as technical lead on software qualification projects, preparing and executing qualification protocols.Support global LIMS upgrades and site projects as required.Compliance, Documentation & Data IntegrityEnsure all LIMS administrative activities safeguard data integrity in line with GMP and regulatory expectations.Complete documentation reviews, including periodic reviews, ERES assessments, SOP updates, and data integrity evaluations.Liaise with Quality teams to ensure system design and changes meet departmental and compliance requirements.Maintain and update QC/QS documentation in alignment with regulatory and site requirements.Training, Investigations & CAPADeliver training to end users, including QC Chemists, on all aspects of the LabWare LIMS system.Investigate system-related non-conformances and provide technical input into associated CAPA activities.Support achievement of relevant KPIs and quality objectives.Safety, Compliance & Continuous ImprovementPromote a culture of safety and regulatory compliance across all LIMS-related activities.Ensure compliance with cGMP, ISO 14001, ISO 45001, Health & Safety and Environmental legislation, and all site policies.Contribute to continuous improvement initiatives within the QS and QC environments.Perform additional duties as assigned by the Quality Services Lead.Minimum RequirementsDegree in a Science or Engineering discipline.3–5 years' experience performing administrative activities on a LabWare LIMS system.Completion of the LabWare LIMS Administrator Level 1 System Administration course.Strong communication skills with proven ability to collaborate effectively across teams.Ability to work independently with strong initiative as well as part of a team