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Claran Consultants Ltd in Cork seeks an Engineering Document Control Specialist for a biopharma facility. You will report to the Core Projects Manager and oversee the control of the engineering documentation system.
This is initially a 12-month contract. Responsibilities include maintaining the Engineering Documentation Control Centre, drafting controlled documents with Veeva and Trackwise, and ensuring proper archiving and regulatory compliance.
Document control specialist is required for a biopharma facility in Cork. The Engineering Document Control Specialist will report to the Core Projects Manager and is responsible for the control of the engineering documentation system. Initially a 12-month contract.
A Bachelor's Degree in the relevant technical field 1-2 years' industry experience in a GMP environment Strong written and verbal communication skills, with a keen eye for detail
GMP Bsc Veeva Trackwise TPBN1_IJ