Our client is seeking a highly motivated and detail-oriented contract resource to assist in converting paper-based GMP fillable forms and logbooks into digital, audit-trailed records using an in-house digital solution. This role is critical to supporting compliance, operational efficiency, and digital transformation within regulated environments.ResponsibilitiesDigitise GMP forms and logbooks.Ensure accurate version control and metadata tagging for compliance.Apply advanced spreadsheet-like techniques (e.g. formulas, conditional formatting, data validation) to support automation and data integrity.Maintain high productivity and quality in completing daily assigned tasks.Collaborate with internal teams to understand form requirements and workflows.Support & maintenance of central repository of common formulae & conditional formats.Review & test the work of other peers to ensure it has been set up properly.Support development & maintenance of dashboards to monitor performance.ExperienceFast learner/adopter of new computer systems.Proficiency in Microsoft Excel or equivalent spreadsheet tools.Experience formatting Word documents (tables, fonts, resizing, pagination, etc.).Strong self-discipline and motivation to complete piece work independently.Excellent attention to detail and ability to follow SOPs & compliance rules without supervision.Clear and effective communication skills, especially for training and documentation.Ability to work methodically and consistently in a regulated environment.Professional English speaker/writer.Prior experience in pharmaceutical, GMP, or GxP-regulated environments.Familiarity with digital document systems or form automation platforms.Experience working in prior digitization projects.To discover more about this opportunity please apply online or contact Darragh on for a confidential discussion.