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!!