PpAs a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose‑driven innovation, and world‑class products can shape the future direction of healthcare. /p pAt Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com. /p h3bPosition Summary /b /h3 pWe are looking for an experienced LIMS Application Manager to take ownership of our LabWare LIMS environment across two manufacturing sites (Switzerland and Germany). The role sits within the IT Production Systems team and covers day‑to‑day application management, GxP compliance, and active participation in an ongoing platform migration and LIMS version upgrade. You'll be working in a regulated medical device environment (FDA 21 CFR Part 11, EU Annex 11, ISO 13485) and coordinating closely with internal stakeholders, system vendors, and external implementation partners. /p ul liEnsure stable operation of laboratory applications and information systems under your ownership /li liProcess incoming requests (Incidents, Service Requests, Change Requests) in a timely manner /li liMonitor application availability, performance, recoverability, and resource consumption /li liCommunicate proactively with users and IT Support on disruptions or planned downtime /li liSupport and consult users on application and process handling /li liCoordinate between support teams, application developers, and local Application Managers /li liContribute to global KPIs and strategic planning for updates and releases /li liSupport specification, testing, and rollout of new updates and releases /li liEnsure all operational documentation is defined and maintained (operations manuals, user guides, guidelines) /li liEnsure system compliance with FDA 21 CFR Part 11 and EU Annex 11 /li liAssess and proactively mitigate application‑related risks /li /ul h3bEducation / Experience Requirements /b /h3 pDegree in Business Informatics, IT, or a comparable technical qualification /p p3–5 years of experience in application support, maintenance, or application lifecycle management /p pExperience in project management, process management, or requirements engineering /p pBackground in aGxP‑regulated environment (GAMP 5, 21 CFR Part 11, EU Annex 11) /p h3bSpecialized Skills / Other Requirements /b /h3 pGood understanding of laboratory processes (sample management, instrument integration, data management) /p pComputer System Validation (CSV) experience is mandatory /p pExperience in the medical device or pharmaceutical industry (ISO 13485, EU MDR/IVDR) is an advantage /p pBasic knowledge of database technologies (MS SQL Server or Oracle) and application architecture /p pFamiliarity with SAP interfaces or ERP‑integrated environments is a plus /p pTeleflex is an equal opportunity employer. Applicants will be considered without regard to age, gender, race, nationality, ethnicity, civil status, family status, sexual orientation, disability, religion and/or membership of the traveller community. /p pIf you require accommodation and support to apply for a position, please contact us at /p /p #J-18808-Ljbffr