Description
One of our key global clients, a leading Medical Device company, located in the Galway area,have an immediate opening for a Quality Engineer on a contract basis. This would be an initial 3 month contract role.
The Quality Engineer will have the following responsibilities:
* Overall responsibility for production GMP standards and compliance.
* Investigation of root cause and following through on effective corrective actions to prevent re-occurrence for customer and internal quality issues.
* Establishing inspection standards, plans, frequencies and test methods.
* Establishing and maintaining FMEA's.
* Preparing and updating Operations procedures and associated documentation.
* Reporting area of responsibility metrics.
* The quality engineer will perform an active role in quality planning and new product introduction from a quality perspective.
The Quality Engineer must meet the following requirements:
* Degree in Quality Assurance or Degree in Science / Engineering.
* Experience within a similar role as quality engineer.
* 3+yrs industry experience in a medical device-manufacturing
* Working knowledge of FDA and ISO Quality systems for Medical device companies.
* New product introduction and manufacturing process transfer experience would be a distinct advantage.
This is an exciting opportunity to work with one of the worlds leading medical device companies, if you feel that you would be suited
to this role please contact me Derek Sheridan ASAP on to be considered for interview.
To find out more about Real please visit www.realstaffing.com