Arcadis is seeking a Quality Documentation Specialist for a Pharmaceutical assignment in Cork, Ireland. The role supports the Document Control Team on-site for an initial 12-month contract. Responsibilities include overseeing document control processes in compliance with GMP, managing electronic documents, and coordinating reviews and approvals. The position offers a hybrid working model, allowing for 3 days of work from home and 2 days onsite. Ideal candidates have 3+ years in document management in a regulated industry and knowledge of relevant regulatory requirements.
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