Document Controller

I am partnering with a biopharma client to offer a fantastic partime contract opportunity for a Document Controller to join their Cork-based team. Key ResponsibilitiesManage and maintain the Engineering Document Control Centre to ensure compliance and accessibility. Oversee the distribution, tracking, and secure archiving of project and site drawings. Implement and administer the document numbering system for commissioning and restart documentation. Prepare, review, and issue controlled documentation using systems such as Veeva and Trackwise. Ensure appropriate procedures are followed when documents are removed from the Engineering Control Centre.

Coordinate the receipt and issuance of engineering and vendor documents to and from the central documentation hub. About You – Key Qualifications and SkillsDegree in a scientific, engineering, or related discipline (BA/BS or equivalent). Minimum of 3 years’ experience in document control or a related engineering function within the biopharma or pharmaceutical sector. Strong communication skills, both written and verbal, with the ability to work effectively across teams. Confident using document management systems and standard business software.