Laboratory Syst Tech Specialist

TERUMO BCT, INC; Millbrook; A distancia; GBP 42.000 - 62.000; Jornada completa

Descripción de la vacante

TERUMO BCT, INC is seeking a Laboratory Systems Technical Specialist for the Larne site in Northern Ireland. The role involves leading the deployment and configuration of a Laboratory Information Management System (LIMS) within the QC laboratory, acting as the primary liaison between the Larne site QC lab, IT, the Global Project Team and external vendors.

The successful candidate will develop and maintain LIMS master data, analyze workflows, and drive process improvements, data integrity, and

Formación

• GMP-regulated QC lab experience preferred.
• Degree in Chemistry or closely related subject required.
• Experience with LIMS, data management and regulatory requirements desired.

Responsabilidades

• Lead end-to-end QC LIMS implementation and configuration.
• Collaborate with QA, IT, project teams and vendors to gather requirements.
• Develop and maintain master data and data structures in LIMS.
• Support data migration, validation and UAT activities.
• Create reports and dashboards to monitor QC performance.

Conocimientos

Prioritisation

Deadline driven

LIMS

Educación

Chemistry degree

Herramientas

LIMS

Descripción del empleo

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Laboratory Syst Tech Specialist

Date: Oct 26, 2026

Laboratory Systems Technical Specialist

12 Month Fixed Term Contract

(26_36)

Terumo BCT is a Global leader in blood management, blood safety, therapeutic apheresis, cell therapy and cell collections. We have an exciting opportunity for a Laboratory Systems Technical Specialist to join Terumo BCT- Larne. Come join us today!

The Laboratory Systems Technical Specialist will be responsible for leading and executing the activities required for successful implementation, configuration and deployment of a Laboratory Information Management System (LIMS) within the Quality Control (QC) laboratory at Terumo BCT Ltd. Larne. The role serves as the primary liaison between the Larne site QC laboratory, IT, the Global Project Team and the external vendor to ensure the system is designed, configured, and optimized to support compliant laboratory processes executed by the Larne site.

The successful candidate will be responsible for developing and maintaining master data and static data within the LIMS, analysing current laboratory workflows, identifying opportunities for process improvement and driving efficiencies through system automation and standardisation. This role requires a strong understanding of QC laboratory operations, data management, GMP requirements and computerized system implementation.

Core Responsibilities

• Support the end-to-end implementation of the QC laboratory LIMS solution.
• Collaborate with laboratory personnel, Quality Assurance, IT, the Global Project Team and vendors to gather and document business and user requirements.
• Configure and maintain LIMS workflows, specifications, sample plans, product structures, test methods and reporting tools.
• Build, review and maintain all static and master data required to support QC laboratory operations.
• Support data migration activities including data cleansing, verification and reconciliation.
• Participate in system testing activities including user acceptance testing (UAT), defect resolution and system verification.
• Support computerized system validation activities in accordance with GMP and company requirements.
• Evaluate existing laboratory processes and identify opportunities to improve efficiency, compliance, data integrity and user experience.
• Develop and implement streamlined workflows that reduce manual activities and improve data visibility.
• Drive standardisation of laboratory processes across functions where appropriate.
• Monitor system performance and recommend enhancements to maximise value from the LIMS platform.
• Establish and maintain accurate laboratory master data, ensuring consistency and compliance.
• Develop reports, dashboards, and metrics to support operational performance monitoring and decision making.
• Support trending and analysis of laboratory data to identify process improvement opportunities.
• Ensure laboratory data structures support regulatory, quality, and business requirements.
• Ensure all activities comply with GMP, data integrity and regulatory requirements.
• Support the creation and review of SOPs, work instructions, validation and training materials.
• Support change control activities related to the laboratory system implementation.
• Provide training and ongoing support to laboratory users.
• Build strong relationships with laboratory, quality, manufacturing, and IT stakeholders to ensure successful implementation and adoption

Education

• A degree in Chemistry or closely related subject

Experience

• Experience working within a GMP-regulated Quality Control laboratory environment
• Strong understanding of laboratory workflows, sample management, testing processes and data management principle
• Knowledge of computerized system validation, data integrity, and regulatory requirements
• Experience with process mapping, workflow optimisation and continuous improvement methodologies

Skills

• Ability to manage multiple priorities
• Ability to work to strict deadlines

You must clearly demonstrate on your CV / application how you meet the required criteria as failure to do so may result in you not being shortlisted.

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