Quality System Coordinator

Brightwater

Waterford

A key client in the Medical Device industry has a 12 month contract available for an experienced Quality System coordinator or document controller. Working as part of a dynamic new project team you`ll be working to develop and implement the changes required by the new European Medical Device Regulations. Based in Waterford, this team with have a global remit that spans numerous sites in various countries. Key Responsibilities: Update Quality documentation as requested by the project. Manage all documentation changes for MDR project. Ontime delivery of the schedule. Change management activities for the implementation of MDR QMS requirements. Requirements: 3-5 years experience working with a regulated Quality System. Previous experience of implementing documentation changes. Cross functional project team experience. Working Knowledge of MS office. Working knowledge of change management systems/processes and documentation management. Good communication skills ( verbal & written ) Decisive, self-motivated/capable of working on own initiative, and able to prioritise and a proactive approach. High attention to detail. Medical Device experience. cGMP. For more on the role call Nigel on 021 4221000 or send your CV for consideration. This job originally appeared on RecruitIreland.com.

2248 days ago