One of my clients is currently recruiting for a Quality Engineer. You will be responsible for monitoring all the operational aspects of the quality system and where appropriate, using relevant quality tools to support business activities to improve the operational effectiveness.

You will have the following experience and qualifications:

-Experience in a quality role within a high volume medical-device manufacturing controlled environmental
-Knowledge of six sigma and lean manufacturing principles
-Educated to either degree level or equivalent
-Evidence of continued professional development
-Advanced knowledge of MS office and Minitab #

Your responsibilities will include the following:

-Use six sigma continuous improvement techniques to implement suitable corrective / preventive actions to reduce quality issues
-Support both operations and engineering departments in cross-functional teams.
-Develop and issue control plans, quality documentation and visual aids.
-Provide training and development for SPC on production processes.
-Support cross-functional activities in the execution of validations.
-Provide quality engineering support for the internal audits, third party regulatory audits and customer complaints as required
-Actively support/ lead the development and maintenance of the companies quality systems (SAP/SFOL/QDMS)
-Ensure the detail and content of the Quality Notifications / MRB decisions conform to the relevant procedural documentation.
-Audit / authorise release of the document history records for each production batch.
-Maintain and develop the BOS quality performance documentation as required

Validation experience is essential.

Job Type : Contract/Interim

Location : Plymouth, Plymouth

Salary : 36k pa

Date Advertised : 24 Nov 2012

Sorry, this position is no longer available.

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