Description
An exciting new opportunity has become available for a Quality professional within the medical devices expereince. Candidates will be require to have quality experience within a medical devices background.Quality Engineer ;
- Deal with and manage Quality Managment Systems and maintain appropriate and comprehensive quality process specifications .
- Document and maintain in good order all relevant Quality sections of Device Development History File and DMR as directed by Document Control
- Assist and where appropriate lead in the compilation and execution of validation protocols for new product/processes and software.
- Medical device & ISO 13485 experience.
- Assist with Audit.
Quality Requirements;
- Medical Device experience
- Experience either hosting or being involved in intenal and external audits
- Must have an engineering background in manufacturing, with a proven ability to interpret and create engineering specifications and procedures
- ISO 13485
If you are interested in this role, have any questions about this position or would like to register your interest in other positions, please feel free to send your up to date CV or contact me on
To find out more about Real please visit www.realstaffing.com