Lab Systems Specialist

Job Description Tittle: Lab Systems Specialist Location: Dublin, Ireland Contract Duration: 12-month contract Rate: 22.00 Hourly Looking to build your career at the intersection of laboratory operations, digital systems, and pharmaceutical manufacturing? This opportunity offers hands-on exposure to cutting-edge QC laboratory systems, system implementation projects, data integrity initiatives, and cross-functional collaboration within a highly advanced GMP biologics environment. Key Responsibilities Create, maintain, and review master/static data within laboratory systems Support change management activities associated with laboratory systems and workflows Participate in the rollout and implementation of new laboratory systems across QC laboratories Support system configuration, user acceptance testing (UAT), training, and go-live activities Troubleshoot and resolve laboratory system issues and support end users Assess system impacts associated with method/specification changes and change controls Execute and document system changes in line with GMP and procedural requirements Collaborate with laboratory, manufacturing, quality, analytical support, and IT teams Support integration activities between lab systems and interfacing platforms Contribute to operational excellence and continuous improvement initiatives Assist with development and review of SOPs, work instructions, and training materials Provide training and ongoing support to laboratory users Support metrics tracking, reporting, and visibility of laboratory system activities Participate in small to medium-sized projects and support project planning activities Requirements Bachelor's degree in Science, Engineering, Computer Science, or related discipline 2-4+ years' experience within a GMP-regulated pharmaceutical or biotechnology environment Experience working with laboratory systems such as Empower, LIMS, LES, MODA, CIMS, or similar Understanding of laboratory workflows, system interfaces, and data management Experience supporting system implementation, UAT, training, or system rollouts Strong understanding of cGMP, data integrity, and regulatory requirements Experience with change control, CAPA, and quality systems Exposure to biologics or pharmaceutical manufacturing environments Knowledge of QC laboratory operations and analytical testing workflows Experience supporting digital laboratory transformation or continuous improvement initiatives is advantageous Ability to troubleshoot system issues and independently manage assigned activities Excellent communication, collaboration, and organisational skills Strong attention to detail and problem-solving capability Ability to manage multiple priorities within a fast-paced environment We're actively shortlisting, apply now or get in touch today to avoid missing out!!