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: ØStrong communication and organisational skills required ØExperience with QMS and EDMS systems ØHighly proficient with MS Office Suite ·particularly Excel - metrics generation is desirable.
Ø2 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 send your updated CV to