Quality Assurance Document Control Specialist: On behalf of our Client, Kenny-Whelan is hiring a QA Document Control Specialist to join a Global BioPharmaceutical Company in Cork. Contact:Carmel Synnott on email: or call on Profile of the Role: 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. Main duties and 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 Skills and Experience: Strong communication and organisational skills required Experience with QMS and EDMS systems Highly proficient with MS Office Suite *particularly Excel - metrics generation is desirable. 2 to 3 years experience working in the Pharmaceutical/BioPharmaceutical industry *** Are you eligible to work in Ireland? As this is a Contract role, you will need a Visa: either Stamp 1G or Stamp 4 *** All applications will be treated with the strictest confidence Kenny-Whelan Contact: For further information please contact Carmel Synnott on or sendyour updated CV to Skills: EDMS ExceMS office Benefits: Paid Holidays Canteen