I am partnering with a biopharma client to offer a fantastic contract opportunity for a Document Controller to join their Cork-based team.
Key Responsibilities
* Manage 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 Skills
* Degree 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.
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