Position Description Title: Quality Engineer Validation
Main areas of responsibility:
− 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 introductions
− 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.
3. Education and Experience Required for Role
− Bachelors degree from accredited college
− 3/5 yrs in a Quality function within the Medical Device/ Pharmaceutical industry.
− Have good knowledge of statistical techniques in the use of problem solving/ data analysis.
− Have a proven track record in development/execution of Validation programs in areas of Equipment, Process and Information management
− Ability to demonstrate standards of leadership – Managing Complexity/Credo Values/Innovations/Customer focus.
− Team Player
− Good Influencing Skills
− Project Management Skills
− Good generalist
− Good communication skills
If you would like further Information you can contact the recruiter directly:
Sean McCarthy | Tel: +353 (0) 212339371