This is a great opportunity for an experienced Quality Engineer to join a rapidly growing medical technology business just outside of Bath.
The successful Quality Engineer will be responsible for managing changes to ensure that manufacturing quality is improved in order to enable strategic success.
You will possess a strong background of Quality in either an IVD or medical devices industry and will have a minimum of 5 years' experience. It is essential that you have direct knowledge of ISO 13485:2016 and FDA 21 CFR Part 820.
Quality Engineer Requirements:
A minimum of 5 year hands on experience Full knowledge of process validation In-depth knowledge of ISO 13485 and FDA 21 CFR Part 820 Risk management experience
If you are interested in this Quality Engineer opportunity, click Apply Now and we will be in touch with you soon.