LIMS Project Lead: GMP QC & LabWare Specialist

Chanelle Pharma; Loughrea; On-site; EUR 55,000 - 75,000; Full time

Job summary

Chanelle Pharma in Loughrea, Ireland, seeks a LIMS Administrator on a 12-month on-site contract to drive LabWare LIMS across QC labs. You will support configuration, validation, deployment, and ongoing optimisation, acting as the bridge between laboratory operations, quality systems, IT, and vendors.

The role requires GMP QC experience, familiarity with LabWare LIMS, and a drive to enhance compliant, efficient workflows. Reports to the QC manager.

Qualifications

• Bachelor’s degree in a relevant scientific discipline.
• Minimum of 5 years' GMP pharmaceutical QC laboratory experience.
• Experience with LabWare LIMS is desirable; Waters Empower is a plus.

Responsibilities

• Lead LIMS project design, configuration, testing, validation, and deployment.
• Support data migration, reporting structures, and system improvements.
• Provide QC expertise across materials, in-process and finished products.
• Ensure GMP compliance and liaise with IT, QA, and external vendors.

Skills

GMP Quality Control

LabWare LIMS

Waters Empower

Cross-functional teamwork

Regulatory compliance

Analytical thinking

Education

Bachelor's degree in Chemistry/Analytical Chemistry/Pharmaceutical Sciences/Life Sciences

Tools

LabWare LIMS

Waters Empower

ERP integrations

Job description

Chanelle Pharma in Loughrea, Ireland, seeks a LIMS Administrator on a 12-month on-site contract to drive LabWare LIMS across QC labs. You will support configuration, validation, deployment, and ongoing optimisation, acting as the bridge between laboratory operations, quality systems, IT, and vendors.

The role requires GMP QC experience, familiarity with LabWare LIMS, and a drive to enhance compliant, efficient workflows. Reports to the QC manager.