Senior AIT Laboratory Manager
Duration:
12 months (start date: 3 February 2026)
Location:
Cruiserath, Dublin
Working hours:
39 hours per week
Onsite requirements:
Onsite
Engagement Type:
LTD Company Contractors ONLY
Hourly Rate:
€87.18
Legal Right to Work - Applicants must have the legal right to work in the location of the assignment. No sponsorship available.
Atrium Global is supporting a client in the pharmaceutical industry to secure an experienced professional for this position.
Job Overview
The role involves providing compliant support for Lab IT and benchtop analytical equipment within a regulated laboratory environment. Working closely with cross functional teams, you will ensure systems meet industry and corporate compliance standards while contributing to the implementation, configuration, and commissioning of laboratory technologies.
RESPONSIBILITIES
* Ensure all Lab IT and benchtop analytical equipment activities comply with 21 CFR Part 11, EU Annex 11, cGLP/GMP, and corporate requirements.
* Support the introduction and implementation of new laboratory instrument systems.
* Collaborate with QA, QC, CSV, Engineering and external vendors to deliver compliant solutions.
* Work with external laboratory suppliers to assist, configure and commission benchtop equipment, taking ownership from delivery through to commissioning.
* Act as a technical design engineer for Lab IT, GMP and regulatory systems, including integrations with Chromatography and benchtop analytical instruments.
* Work under the direction of the IT Applications Manager and alongside corporate laboratory systems teams to deliver systems and interfaces.
REQUIREMENTS
* Degree in Engineering, Information Systems, Computer Science or Life Sciences.
* Minimum of 4 years experience in a pharmaceutical laboratory environment, including IT support for laboratory instrument systems.
* Experience with Solovpe, FIT, Osm and Raman systems.
* Strong working knowledge of Windows file permissions, networking, Active Directory and Group Policies.
* Background working within GMP Quality Management Systems in laboratory or manufacturing settings.
* Strong organisational skills with the ability to work at pace and meet deadlines.
* Excellent leadership, communication, critical thinking and customer engagement skills.
* Ability to adapt to changing business needs and work effectively within a team.
* Experience managing multiple operational issues simultaneously.
* Able to work independently and remotely with minimal supervision.
* Thorough understanding of pharmaceutical regulations including cGMP/cGLP, OSHA, EPA/EQB, 21 CFR Part 11 and EU Annex 11.