6-Month ContractChanelle PharmaLocation: Ireland / Hybrid (regular on-site presence required)Start: ASAPKorn Ferry Interim is supporting our esteemed Life Science client in the search for an experienced LabWare LIMS Consultant / QC Systems Specialist to join on an initial 6-month contract.This role will play a key part in stabilising and supporting a critical LabWare LIMS implementation currently approaching go‑live. The successful contractor will bring a rare blend of LabWare system expertise and practical QC laboratory understanding, helping to strengthen internal capability, support validation activity, improve documentation, and ensure the business is set up for a safe and sustainable deployment.This is a hands‑on role suited to someone comfortable operating across IT, laboratory, validation, and end-user training in a regulated GxP/GMP pharmaceutical environment.Key ResponsibilitiesProvide hands‑on support to the ongoing LabWare LIMS implementationHelp stabilise the project and support the business through a critical pre‑go‑live phaseSupport validation activities, including OQ‑related documentation and scriptingWork closely with QC and laboratory users to ensure the system supports operational needsDeliver practical user training and help raise internal capability across the teamDevelop, refine, and improve work instructions, SOPs, and supporting documentationSupport issue resolution, process clarification, and day‑to‑day coordination between business and technical stakeholdersAct as a visible, on‑site point of support during testing, readiness, and deployment activityHelp embed knowledge internally to reduce long‑term reliance on external supportExperience RequiredStrong hands‑on experience with LabWare LIMSPrior experience supporting LIMS implementation, enhancement, or go‑live activity in a regulated environmentGood understanding of QC laboratory processes within pharma / life sciences Experience supporting CSV / validation activities, ideally including OQ documentation / scriptingAbility to work directly with laboratory users and translate operational needs into practical system/process support Experience producing and improving SOPs, work instructions, training materials, and process documentation Strong stakeholder management skills with the ability to work across IT, QA, QC, and project teams Comfortable operating in a hands‑on, delivery‑focused environment with a mix of technical and business responsibilitiesPreferred ExperienceExperience in pharmaceutical manufacturing or another highly regulated life sciences environment Previous involvement in LabWare administration / configuration support Experience supporting training, adoption, and knowledge transfer Prior exposure to go‑live readiness, cutover support, or post‑implementation stabilisation
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