Job Ref: 214707984

Date: 2021-09-21 11:31:42

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We are a market leading Medical Device Manufacturer and due to our continued growth, we have an exciting opportunity for a Quality System Engineer to join the team. 

As our new Quality System Engineer, you will be a part of our established Quality and Regulatory Team, with your responsibility for the ongoing maintenance and development of our Quality Management System (ISO 13485). This is an excellent opportunity for an Experience Medical Device Quality Professional who is looking to continue their career progression, or an experienced Quality professional from another Highly Regulated Manufacturing environment who is keen to build a career in the Medical Device Sector.  

To be successful in this role, you will have a prior experience of working in a Quality Engineering or Quality Assurance role within a Highly Regulated Manufacturing Environment and a strong understanding and knowledge of ISO 13485 or ISO 9001, including the writing of SOP’s and upgrading of QMS.

Essential Experience/Skills/Knowledge:

Prior experience of working in a Quality Engineering or Quality Assurance role in a Highly regulated Manufacturing Environment

Demonstrate ability to communicate and work cross-functionally

Strong Knowledge and Understanding of ISO 13485 or ISO 9001 requirements

Experience in writing Standard Operating Procedures and upgrading Quality Systems

This is a site based position. 

If you have the required skills and experience to be successful, please contact Kris Holmes at Orion

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