Laboratory Specialist

Hiring: Global LIMS (GLIMS) Specialist | Ballydine, Co. Tipperary | Remote Contract Opportunity

Contract Duration: Initial contract until December 2026, with a strong possibility of extension based on business requirements and performance.

Working Model: Primarily remote role; however, occasional on-site attendance in Ballydine may be required for project activities, business needs, workshops, testing, training, or critical support activities.

We are currently seeking an experienced Global LIMS (GLIMS) Specialist to support laboratory information management systems within a GMP-regulated pharmaceutical manufacturing environment.

Key Responsibilities:

• Act as the primary point of contact for LIMS-related support across laboratories and manufacturing operations.
• Manage LIMS change requests and configuration activities through the full change control lifecycle.
• Perform static data configuration and maintenance within the Global LIMS platform.
• Conduct impact assessments, requirements gathering, technical evaluations, and system troubleshooting.
• Support validation activities, SDLC, UAT, data integrity, and regulatory compliance requirements.
• Collaborate with Quality, Manufacturing, IT, Laboratory, and Global Support teams.
• Review and approve technical documentation, protocols, reports, and change records.
• Support inspections, audits, investigations, and continuous improvement initiatives.

Required Experience:

• Bachelor's Degree in Chemistry, Biological Sciences, Computer Science, or related discipline.
• Minimum 4 years of hands-on LabWare LIMS experience within a pharmaceutical or biotechnology environment.
• Strong experience with:

1. LabWare LIMS v6+
2. Static Data Configuration
3. Change Control
4. SDLC & Computer System Validation (CSV)
5. UAT & Validation Documentation
6. GMP / GxP Compliance
7. Data Integrity
8. SQL Query Development

Preferred Experience:

1. • SAP integration exposure
2. • Reporting and analytics tools
3. • Sterile pharmaceutical manufacturing environments
4. • Audit and inspection support
5. • LIMS Basic or scripting experience

Keywords:

GLIMS | Global LIMS | LabWare LIMS | LIMS Specialist | LIMS Analyst | CSV | Validation | GMP | GxP | Data Integrity | SQL | Change Control | Quality Systems | Pharmaceutical Manufacturing | Biotechnology

If you are interested, please send your updated CV along with your availability for a confidential discussion.