About Us:
At Dabster, we specialize in connecting top talent with leading global companies. We are currently seeking a skilled and dedicated
IT Lab Administrator
to join our client's team in
Dunboyne, Ireland.
Our mission is to be the foremost recruitment specialist in securing exceptional talent for a diverse range of global clients.
Who You Will Work With:
Our client is a globally recognized technology company delivering IT services, consulting, and business solutions. They partner with leading organizations worldwide to drive digital transformation, leveraging innovation and deep industry expertise to solve complex business challenges.
Job Description:
Key Responsibilities:
* Provide hands-on support and system administration for lab systems, equipment, servers, desktops, and software in a GxP-controlled environment.
* Troubleshoot complex technical issues involving software, OS, hardware, network, or scientific equipment setups.
* Administer system access requests and maintain user management protocols.
* Author and manage documentation for validation, qualification, and testing (e.g., validation plans, test scripts, qualification protocols - IQ/OQ/PQ).
* Define, document, and support system usage aligned with SOPs and regulatory requirements.
* Ensure compliance with 21 CFR Part 11, EU Annex 11, and applicable Data Integrity standards.
* Collaborate with CSV Lead, Site IT, and System Integrators.
* Support operational readiness teams and agency inspections.
* Provide SME-level troubleshooting, technical direction, and proactive support.
* Monitor systems, backups, and data security, identifying and resolving issues swiftly.
Qualifications & Education:
* Bachelor's Degree or higher in a technical or scientific discipline.
* Minimum 5 years of professional experience in the digital or IT domain.
* Strong multitasking skills and ability to manage competing priorities effectively.
* Proven experience in identifying and resolving operational issues.
* Excellent written and verbal communication skills.
Desired Skills & Experience:
* Minimum 3 years' experience in a similar Lab IT or CSV role within a GxP-regulated environment.
* Hands-on experience with validating, qualifying, and/or using pharmaceutical QC Lab standalone COTS systems.
* Strong understanding of system lifecycle documentation including authoring and administration.
* Proficient in Data Integrity principles and regulatory compliance.
* Experience with system security, data backups, and routine monitoring.
Why Join Us?
* Opportunity to work with a leading global organization at a state-of-the-art biopharma facility.
* Collaborative and technically advanced environment.
* On-site role offering real-time engagement with critical lab operations and stakeholders.
How to Apply
Apply by submitting your resume today, showcasing your relevant experience and passion for the position via LinkedIn Easy Apply or directly to