Description
Medical Devices Quality Engineer
A leading edge medical devices company in Bedford are looking for an experienced quality for a 6 month contract
This company is developing an innovative medical device aimed at drastically improving people's lives.
You will be responsible for authoring and reviewing plans, specifications for design, installation, operational and performance qualification.
Other responsibilities include the planning and execution of supplier reports and audits and problem reports, all within ISO 13485 standards.
The role as Quality Engineer will give you the opportunity to work on market leading medical devices whilst working closely with in house R&D Engineers, external consultants and suppliers to ensure the company's product remains market leading
To be considered for the Quality Engineer role you will:
- Hold an engineering or science related degree
- Understand Agile
- Have previous quality experience within a medical devices environment
- Ideally working to ISO 13485 standards.
If you feel you may be suitable please send in your CV in the first instance