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Job DescriptionA QA Validation Technical Writer is required by Careerwise recruitment to work with our Limerick based biotech client on a 12-month contract position.Role of this position Execution of SIP/ cleaning and continuing validation protocols. Writing and approving Deviations/ GMP documents Technical writing experience in writing site reports. Generate/review/Approval of SIP/ CIP protocols Generation of Summary Reports Assessment of SIP/ CIP issues during study runs and closeout of deviations JOB REQUIREMENTS Relevant 3rd level degree. Minimum of 2 years experience working in a GxP environment. Preferable to have experience in a commercial Biologics Manufacturing site. Experience in SIP/ cleaning validation results reporting review beneficial N.B. It is essential that you hold a valid working visa for Ireland
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