Laboratory Project Engineer
Location: Dublin, Ireland
Contract Length: 12 Months
We partner with pharmaceutical organizations to engineer, integrate, and validate compliant Lab IT and analytical systems, delivering inspection readiness, uncompromising data integrity, and operational excellence.
Key Responsibilities
- Ensure full compliance of Lab IT and benchtop analytical systems with global regulatory standards and corporate policies.
- Support the introduction, validation, and lifecycle management of new laboratory instrument systems.
- Collaborate cross-functionally with QA, QC, CSV, NQC Engineering, IT Applications, and approved contract vendors.
- Partner with external laboratory suppliers to configure, install, and commission benchtop equipment.
- Take full ownership of equipment from delivery through commissioning, ensuring accurate tracking and documentation.
- Act as Technical Design Engineer for Lab IT/GMP/Regulatory systems, including system architecture and integration with platforms such as chromatography and benchtop analytical systems.
- Work under the direction of the IT Applications Manager and alongside the Corporate Laboratory Systems Team to deliver robust system interfaces and integrations.
Qualifications & Requirements
- Bachelor's Degree in Engineering, Information Systems, Computer Science, or Life Sciences.
- Minimum of 4 years' experience within a pharmaceutical laboratory environment, including hands-on IT support for laboratory instrument systems.
- Experience with systems such as Solovpe, FIT, OSM, and Raman technologies.
- Strong understanding of Windows file permissions, networking infrastructure, Active Directory, and Group Policies.
- Experience working within GMP Quality Management Systems in laboratory or manufacturing environments.
- Proven ability to manage workload effectively, meet deadlines, and maintain high-quality standards.
- Excellent organizational, leadership, communication, and critical thinking skills.
- Demonstrated success in collaborative team environments, with flexibility to adapt to evolving business needs.
- Ability to anticipate, assess, and resolve multiple concurrent operational challenges.
- Capable of working independently and remotely with minimal supervision.
- Comprehensive knowledge of pharmaceutical regulations including cGMP/cGLP, OSHA, EPA/EQB, 21 CFR Part 11, and EU Annex 11 as they apply to Lab IT systems.
Ready to elevate your laboratory systems? Speak with our experts today...!!
