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# Operations Laboratory Systems Specialist - Lonza

- **Company:** Jobrapido
- **Location:** Carballino, Spain
- **Contract:** Permanent contract
- **Skills:** Audit Trail, Data Integrity, Network Troubleshooting, Information Technology
- **Published:** October 9, 2026
- **Apply:** https://www.buscojobs.com.es/operations-laboratory-systems-specialist-f-m-d-lonza-en-carballino-ID-374877150

## About the Role

Requisitos principales3-5 years in QC systems, OT/IT, or related areas
Experience with laboratory/QC systems, Data Integrity, and CFR 21 Part 11
System administration, troubleshooting, validation, xkdbapo and compliance in regulated environments
Strong problem-solving and continuous improvement mindset
Excellent collaboration and communication skills
Ability to work with Laboratory/Manufacturing, Engineering, Quality and Maintenance teams
Strong organizational and time-management skills
Native-level Spanish; business-fluent English preferred
collaboration
communication
problem-solving
OT/IT knowledge
QC systems
Data Integrity

## Description

OverviewPara presentar una candidatura, simplemente lea la siguiente descripción del puesto y asegúrese de adjuntar los documentos pertinentes.In this role you lead and optimize laboratory systems projects, supporting qualification, implementation, maintenance, and upgrades.You will guide end users, ensure data integrity and compliant access, and manage change requests and CAPAs.You collaborate across Laboratory, Engineering, Quality and Maintenance teams to standardize procedures and promote a strong safety culture.This position offers impact by shaping how systems enable compliant science and reliable operations in a global life sciences context.ResponsabilidadesLead projects for implementation and modification of laboratory systemsSupport qualification, implementation, maintenance, and upgrades of laboratory systemsSupervise contractors and external service providers, managing schedules, resources, and costsProvide technical support and guidance to end usersMaintain data integrity, audit trails, authorizations, permissions, and backup processesManage Change Requests (CRs) and CAPAs related to laboratory operation systemsTroubleshoot system issues and collaborate with manufacturers and providersAct as SME for Data Integrity and CFR 21 Part 11Contribute to standardization of procedures across laboratory systemsPromote EHS/safety culture and support risk assessments and CAPA implementationRequisitos principales3-5 years in QC systems, OT/IT, or related areasExperience with laboratory/QC systems, Data Integrity, and CFR 21 Part 11System administration, troubleshooting, validation, xkdbapo and compliance in regulated environmentsStrong problem-solving and continuous improvement mindsetExcellent collaboration and communication skillsAbility to work with Laboratory/Manufacturing, Engineering, Quality and Maintenance teamsStrong organizational and time-management skillsNative-level Spanish; business-fluent English preferredcollaborationcommunicationproblem-solvingOT/IT knowledgeQC systemsData Integrity