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Quality Engineer Validation

Location: Cork
Experience:3-4 Years
Job Type:Fixed Term Contract
Salary:Not Disclosed
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May be suitable for: Quality Engineer

Position Description Title: Quality Engineer Validation

2. Responsibilities:
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.
− Flexible
− Team Player
− Good Influencing Skills
− Project Management Skills
− Good generalist
− Good communication skills
− Methodical

If you would like further Information you can contact the recruiter directly:

Sean McCarthy | Tel: +353 (0) 212339371


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