As Senior Quality Systems Specialist, you will be assisting in all aspects of the management of the quality system, ISO 13485. This will include using your expertise to develop and improve the system and the department’s effectiveness. You will have to lead the audit process and get involved in aspects of risk management. Providing training to more junior engineers will also be a significant aspect of the position. The ability to liaise and engage with suppliers will also be helpful as you will be assisting with the supplier management processes. You will also be able to lead the department in the Managers absence.
Key experience includes:
- Knowledge of ISO 13485, ISO 9001 & MDSAP
- Previous experience auditing in an FDA regulated environment
- Previous experience in a manufacturing environment
Then we would love to hear from you!
To apply please send your CV to firstname.lastname@example.org and I will contact you within 7 days if your application is being progressed to the next stage.