We’re currently recruiting for an exciting opportunity with an award-winning 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.
− 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
− A Bachelor’s degree from accredited college
− 3-5 years in a Quality function within the Medical Device/ Pharmaceutical industry.
If interested in this posting please feel free to contact Seán McCarthy on +353 (0)87 798 8480 or firstname.lastname@example.org for further information.