A leading Pharmaceutical / MedTech manufacturing company are seeking an experienced Validation Engineer to join their team on a 6-month contract to support a decommissioning project at their Dublin site.This role will be heavily focused on validation documentation and reporting, including the creation, execution, and completion of all required validation deliverables associated with equipment and/or system decommissioning in a regulated environment. The successful contractor will be comfortable working with a high level of autonomy and operating in a predominantly onsite, days-based role.Key ResponsibilitiesSupport validation activities related to a decommissioning projectAuthor, review, and execute validation documentation, including but not limited to:Decommissioning plans and protocolsValidation reportsTraceability matricesEnsure all validation activities are compliant with GMP and regulatory requirementsLiaise with cross-functional teams (Engineering, QA, Manufacturing) as requiredEnsure documentation is completed accurately, on time, and to a high standardProvide validation input and technical expertise throughout the project lifecycleRequired Experience & Skills4–5+ years’ experience working as a Validation EngineerBackground in Pharmaceutical, MedTech, or other highly regulated industriesPrevious experience supporting decommissioning, equipment lifecycle, or similar validation projectsStrong experience with validation documentation and report writingGood understanding of GMP, regulatory, and quality standardsAbility to work independently with minimal supervisionStrong attention to detail and documentation accuracy
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