LGC Clinical Diagnostics, Inc. is owned by LGC Group, a UK-headquartered life sciences measurement and testing business with >$510m of annual revenue and >3,500 employees globally.LGC Clinical Diagnostics Business Unit is comprised of our operating entities including LGC Clinical Diagnostics, Inc. (f/k/a Maine Standards Company & SeraCare Life Sciences), Technopath Clinical Diagnostics, the Native Antigen Company, API & Thistle QA. Our 400+ employees operate FDA- registered and ISO 13485-accredited facilities in Maine (USA), Massachusetts (USA), Maryland (USA), Tipperary (Ireland), an ISO 9001-accredited facility in Oxford, UK and ISO 17043 facilities in Michigan (USA) and Johannesburg, South Africa.We are committed to improving patient healthcare by offering products and services that support accurate and reliable diagnostic results.Job DescriptionWe are seeking a dedicated and ambitious Formulation Technician to join our world-class Research team in Tipperary, Ireland. This outstanding opportunity enables you to contribute to ground breaking projects in a collaborative and inclusive environment where your skills and ideas are valued.ResponsibilitiesAs a Formulation Technician, you will play a crucial role in our research initiatives. Your duties will include:Supporting the formulation of Multichem Base componentsProgressing allocated projects to conclusion within designated timeframesDaily cleaning and maintenance of production equipmentEnsuring all work aligns with ISO 13485, GMP, and the Technopath Quality Management System standardsGenerating improvement ideas and reporting near missesAssisting in measuring, monitoring, and controlling key parameters that drive team performance in critical metrics, as agreed with Production ManagersMaintaining audit standards on an ongoing basisCompleting work to tight deadlines without compromising qualityAchieving individual goals and targetsCollaborating, communicating, and raising issues as neededAdhering strictly to site rules and proceduresPerforming other related duties as assigned by the managerPromoting a culture of excellence by ensuring all products meet defined quality standards and customer specificationsQualificationsTo be successful in this role, you must meet the following requirements:A relevant third-level qualification or equivalentProven ability to work within compliance frameworksStrong attention to detail and dedication to maintaining high standardsExcellent time management skills to meet tight deadlinesEffective communication and collaboration skillsAbility to generate and implement improvement ideasAdditional InformationWhy Join Us?At LGC Clinical Diagnostics, we offer an encouraging environment. You can develop your technical expertise, contribute to important work, and grow your career globally.Benefits25 days' holidayLife assurance and health allowanceDiscounts with local and national retailersFree 24/7 Employee Assistance ProgrammeRecognition schemes and monetary awardsGreat long-term career opportunitiesOur DedicationLGC promotes an environment of inclusion, cooperation, and respect. We believe that a variety of perspectives results in improved outcomes and welcome applications from individuals of all backgrounds. We are an equal opportunity employer and offer reasonable accommodations during the recruitment process – please inform us if you need any modifications.Join us in advancing science and improving lives through diagnostic innovation