Quality Engineer

Republic of Ireland  ‐ Onsite
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Description

Requirements of the role:

To perform supplier quality audits and manage the supplier corrective action process.
TO develop, monitor and identify supplier non-conformance trends.
To manage and drive continuous improvement activities focusing on supplier quality.
Identify and leverage best practices in relation to Supplier Quality Management.
Liaise with Procurement function to develop and execute Supplier Development Programmes such as: Supplier Sourcing; Supplier Approval; Supplier Management, etc.
Ownership and reporting on all quality issues associated with suppliers.
Assesses compliance systems on ongoing basis to identify opportunities for process improvement.

To coordinate investigation activities to ensure root causes are identified and that corrective actions are appropriate.

Essential:

Bachelor's degree in Science, Engineering or is required.
At least 5+ years experience in a Quality Engineering role in a high volume manufacturing environment is required.
Experience in GMP manufacturing environment in Medical Device/Pharma industry.
A certified ISO auditor in a regulated environment is desirable.
Knowledge and experience of process validation.
Six Sigma Green Belt would be an advantage.

This is an urgent and exciting opportunity with competitive hourly rates. If you would like to apply please contact Sarah Irvine on or submit a copy of your CV.
Start date
05/2015
From
Real Staffing
Published at
07.05.2015
Project ID:
899784
Contract type
Freelance
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