Role Title:IT Laboratory Systems EngineerRole Type:12 month contractLocation:Dublin 15We are currently recruiting a IT Laboratory Systems Engineer for a Biopharmaceutical Manufacturer in Dublin 15. The IT Laboratory Systems Engineer is required to support, the introduction of new, Instrument Systems in the Laboratories. They will work closely with Quality Assurance, Quality Control, Computer System Validation, and IT functions to ensure the ingoing operation and compliance of the laboratories systems.Ensure that all work on Lab IT and Benchtop Analytical equipment is carried out in a compliant manner, meets 21 CFR Part 11, EU Annexe 11, cGLP/GMP's, and Corporate & local compliance requirements.Support the introduction of new instrument systems.Work with all departments, QA, QC, CSV, NQC Engineering, and with contract vendors.Working with external laboratory suppliers to assist, configure and commission benchtop equipment. Take ownership of equipment in receiving deliveries and keeping track from delivery to commissioning.Technical design engineer for the Lab IT/GMP/Regulatory systems including integration to other systems such as Chromatography and Benchtop analytical equipment. Work under the direction of the IT Applications manager and with other team members from the corporate laboratory systems team to deliver systems and interfaces.Degree in Engineering, Information Systems, Computer Science or Life Sciences.At least 4 years' experience of working in a pharmaceutical laboratory environment, with IT experience of laboratory instrument systems.Experience with Solovpe, FIT, Osm, Raman systems.Good working understanding of Windows file permissions, networking, Active Directory, Group Policies.Experience of working in GMP Quality Management Systems in laboratory or manufacturing environment.Ability to keep work pace and meet deadlines. Good organising and planning skills.Strong leadership, communication skills, critical thinking, and customer management skills.Proven success working well in a team environment with flexibility to react to changing business needs.Ability to anticipate, evaluate and resolve multiple, simultaneous operational issues.Ability to work independently and remotely with minimum direct supervision.Thorough knowledge of Pharmaceutical Industry Regulations (cGMP/cGLP, OSHA, EPA/EQB), 21 CFR 11 and EU Annex 11 as they relate to Lab IT systems.