Onsite LIMS Project Lead – GMP QC & LabWare

Uniting Holding

Loughrea

On-site

EUR 70,000 - 90,000

Full time

6 days ago
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Job summary

Uniting Holding seeks a LIMS Administrator to support the implementation, validation and ongoing optimisation of LabWare LIMS across QC labs. You will link laboratory operations with IT and vendors to ensure compliant, efficient workflows and data integrity.

The role requires GMP QC experience, QMS familiarity, and hands-on LabWare LIMS/Waters Empower knowledge, reporting to the QC manager. On-site work in Loughrea, Co Galway.

Qualifications

  • Bachelor’s degree or equivalent in Chemistry, Analytical Chemistry, Pharmaceutical Sciences or life sciences.
  • Minimum 5 years in GMP pharmaceutical QC laboratories.
  • Experience with regulated QMS and computer system validation.

Responsibilities

  • Lead LIMS project activities: design, configuration, testing, validation, deployment, and post-go-live support.
  • Configure LIMS workflows, master data, sample lifecycle, and reporting structures.
  • Translate lab and business requirements into functional specs and test scripts.

Skills

GMP knowledge
LabWare LIMS
Waters Empower
QC collaboration
Documentation

Education

Bachelor’s degree in Chemistry/Analytical Sciences

Tools

LabWare LIMS
Waters Empower

Job description

Uniting Holding seeks a LIMS Administrator to support the implementation, validation and ongoing optimisation of LabWare LIMS across QC labs. You will link laboratory operations with IT and vendors to ensure compliant, efficient workflows and data integrity.

The role requires GMP QC experience, QMS familiarity, and hands-on LabWare LIMS/Waters Empower knowledge, reporting to the QC manager. On-site work in Loughrea, Co Galway.

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