Arcadis is seeking a Quality Documentation Specialist for a Pharmaceutical assignment located in Ringaskiddy, Cork. This is initially a 12-month contract with hybrid working options, where 3 days are WFH and 2 days onsite.The successful candidate will be responsible for document control tasks in compliance with Good Manufacturing Practice (GMP). Key responsibilities include managing the Electronic Document Management System (EDMS), preparing documents for archiving, and supporting compliance audits.Exceptional candidates will have a scientific/technical qualification and a minimum of 3 years’ experience in the pharmaceutical sector.
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