Occupli is partnering with a leading multinational pharmaceutical manufacturing organisation to source an experienced Validation Engineer for a 12-month contract assignment.This role will play a critical part in delivering validation activities across key projects, with a strong focus on equipment performance qualification, including cleaning and sterilisation processes.Key ResponsibilitiesLead planning and execution of Equipment/Engineering Performance Qualification (EMPQ) activitiesDevelop Validation Master Plans and associated validation lifecycle documentationAuthor and execute validation protocols and comprehensive summary reportsAnalyse validation data and provide clear technical conclusionsUpdate and improve SOPs and validation documentation as requiredTroubleshoot and resolve technical challenges during study executionCollaborate effectively within cross‑functional project teams while also operating independentlyRequirementsProven experience in EMPQ planning and execution within a regulated pharmaceutical manufacturing environmentStrong technical writing skills with a high level of documentation accuracyAbility to work with minimal supervision and drive deliverables to completionConfident communicator with strong problem‑solving capabilityThis is an excellent opportunity for a validation professional who thrives in a dynamic, compliance‑driven manufacturing environment and can deliver high‑quality results with limited oversight.
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