LSC have a great contract opportunity for a Training Administrator to join a Limerick based Biotech Drug Substance Manufacturing Facility. This is an exciting opportunity to work with next-gen manufacturing technologies, advanced data collection and analysis platforms that will result in safety and quality improvements, increased productivity, and variability reduction. If you have at least 2 years of relevant experience in a cGMP environment and ready for your next challenge, this could be the perfect project for you ABOUT THE PROJECT - KEY RESPONSIBILITIES: Support the continued set up and roll out of the Corporate Training Management System Support activities in the management of training materials, curricula, and learning plans Assist in the creation and management of site procedures in accordance with site Training SOP. Work with other GMP system owners/administrators on the interfaces with the training administration system (for example Veeva Vault, SpeachPharma, Smartsheet). Produce reports from Learning Management System. Ad hoc reports requested by individual learners, leaders, and others ABOUT YOU - ARE YOUR SKILLS A MATCH? Proficient in MS Office applications and training database administration (Experience with Success Factors, ServiceNow an advantage). Familiarity with cGMPs requirements. Strong interpersonal skills. For our contracting positions in Ireland's pharmaceutical industry, applicants must possess a Stamp 1G or a Stamp 4 visa. We apologize for any inconvenience, as visa sponsorship is not available at this time. Thank you for your attention. Apply via this advert or directly at Additionally please contact us at if you have any more questions about this opportunity Skills: Training Administration Learning Management Systems SOP Creation