Our Biopharma client is looking for a QA Document Controller to join the Quality team on a 12 month contract.POSITON SUMMARY:The Quality Assurance Document Control (QADC) specialist is responsible for maintaining and continuous improvement of site quality systems, providing quality oversight of the facility with a focus on document management quality system.RESPONSIBILITIES:Process site-controlled documents on the site Document Control System.Approve document change controls and establish document effective dates.Complete work according to established priorities and policies to assure product documentation is delivered on schedule.Support and train other staff members on the implementation of global improvements related to the Document Control System.Train and support other staff members on the use of the Document Control System.Maintain the Sites Document Store and escalate any potential issues.Control and issue controlled document numbers as required.Support Inspection Readiness for the site and the site in preparation for upcoming inspections.Examine the Quality Metrics related to the Document Control System.Participate and support Continuous Improvement for the Quality Team.Other duties may be assigned as requested.EDUCATION/EXPERIENCE:Strong communication and organisational skills required.Experience with QMS and EDMS systems is desirable.Experience with excel / metrics generation is desirable.