Description
An exciting new opportunity has become available for a Quality Systems Engineer. Candidates will be require to have strong documentation skills and experience within a highly regulated sector such in a pharma, medical device or aerospace industry will be beneficial.Candidates will be required to have a solid background of interpreting and creating specifications and procedures as well as QA Engineering expereince. The position involves the following competencies;
- QA Engineering experience with an awareness of quality systems such as SPC, FMEA, ISO 9001, FDA QSR's, AQL, cGMP's
- producing and maintaining quality process specifications during development and implementation of new products
- Write, maitian and execute QA sections of device development history
- Assist in the execution of validation protocols for new products/processes and ensuring correct implementation.
- Document and maintain QA sections of device development history.
- Assist in the execution of validation protocols for new products/processes.
- Ensuring correct implementation. Manage QA Change control
- Develop and utilise DFMEA/PFMEA and other QA risk analysis techniques to minimise risk.
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