Qa Validation Technical Writer

The role: PE Global is currently recruiting for numerous Technical Writers on behalf of a leading biotech company based in Limerick. This is an initial 12 month contract role.
Responsibilities: Execution of cleaning validation protocols.Taking Cleaning Validation samples alongside Upstream/Downstream processing.Working closely with manufacturing to ensure the CIP/SIP and dirty holds are to the correct times and samples are taken.Generate/review/Approval of CV protocols,Generate ReportsMaintain and update Cleaning Validation PlanSchedule of cleaning activities with ManufacturingLiaise with numerous departmentsEnsure Training is maintained and current.Follow all EHS/Safety SOP/PoliciesActively look for Continuous improvementsExperience: Experienced in QA Validation activities –Extensive experience on writing and approving Deviations/GMP documentsTechnical writing experience in writing site reportsExperience in aseptic techniqueExperience in Gowning for IOS7/ISO8Generating and Executing Validation Protocols.Experience in Validation specifically cleaning validationExperience in assessment of cleaning issues during study runs,Experienced Technical writer,Experience in Deviation/Change control writing,Experienced in coverage testing and clean-into-serviceInterested candidates should submit an updated CV. Please click the link below to apply, call Kellie on 0214297900 or alternatively send an up to date CV to ******
***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***

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