Quality Engineer (Validation Project) - Mayo - 105009
Quality Engineer (Validation Project)
The purpose of the position is to provide Quality Engineering and Process Validation services for Continence products in the Continence Care Plant and so contribute to the growth and profitability of our client Projects will include supporting the qualification of new equipment and up-grades to existing equipment.
Complete Process and Equipment Validation including FAT, SAT, IQ, OQ, PQ protocol development, implementation and report completion.
Conduct process capability assessment as part of process changes management.
Implement process control and ensure process capability is maintained and identify opportunities for process improvement.
Conduct CAPA analysis to determine root cause and complete problem resolution.
Ensure process changes are implemented per change control procedures.
The Ideal Candidate:
Degree (minimum level 8) in Engineering/Science Discipline or Quality Engineering Qualifications
3-5years’ experience in Medical Device Industry utilising high volume automated equipment
Experience in Quality engineering positions.
Ability to participate in cross functional teams
Good working knowledge of medical device quality & regulatory systems and medical device directives
For further information on this Quality Engineer role in Mayo please contact Anna Carty on 086 8168298 / firstname.lastname@example.org
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