The purpose of the position is to provide Quality Engineering and Process Validation services for medical devices to contribute to the growth and profitability of the company, on an 18th month contract.
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 Risk Management / FMEA / Statistical analysis.
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.
Degree in Engineering/Science Discipline
Quality Engineering Qualification
3-5 years’ experience in Medical Device Industry utilising high volume automated equipment
Experience in Quality engineering positions.
Ability to participate in cross functional teams
If you would like further Information you can contact the recruiter directly:
Kevin Silke | Tel: +353 (0) 1 507 9255