We’re currently recruiting for an exciting opportunity with a Medical Device organization based in Limerick. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.


Duties

− Responsible for supporting the activities of Operations / Engineering / Information Management in building product Quality into our products and assuring compliance to the pertinent regulations while at the same time attaining operational effectiveness
− Work with the various departments/groups in development and execution of validation activities associated with new equipment/product or I.M. system upgrades
− Runs /Manages complaint investigation and resolution of same
− Designs and develops validation documentation to support business continuity, new process/product introductions and process improvement requirements
− Implementation and co-ordination of the change control process promotes timely approval of all supporting documentation
− All employees are responsible for minimising both the Environmental and Health & Safety effects of the work that they perform.

Education & Experience

− Be very familiar with the relevant regulatory standards (F.D.A. - Quality System regulations, ISO 13485) applicable to the manufacture of Class III medical devices to Global markets.

If interested in this posting please feel free to contact Seán McCarthy on +353 (0)87 798 8480 or [email protected] for further information.