Quality Engineer

Mayo  ‐ Onsite
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Description

I have an immediate opening for a Quality Engineer with a leading medical device company based in Co Mayo. This is a permanent position offering ambitious Quality engineers the opportunity to grow and develop within an innovative company where excellent training is provided.

The purpose of this role is to provide Quality Engineering and Process Validation service services for a wide range of products.

Responsibilities:

- Complete Process and Equipment Validation including DV, IQ, OQ, PQ protocol development, implementation and report completion.

- Develop product specifications / drawings / quality plans in conjunction with NPD and project team.

- Conduct Risk Management / FMEA / Statistical analysis.

- Complete ISO 13485 / FDA and QSR internal audits per annual schedule.

- 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.

- Personnel training.
Qualifications:

- Degree in Engineering/Science Discipline

- Quality Engineering Qualification

- Experience in statistical analysis / process validation

- 3-5 years experience in Medical Device Industry

- Ability to participate in cross functional teams

If you are interested in hearing more about this opportunity please apply directly to this advert or contact Derek Sheridan on for further information
Start date
04/2015
From
Real Staffing
Published at
11.03.2015
Project ID:
865388
Contract type
Permanent
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