I am looking for a Quality Manager to join my client who is a Bristol-based biotech developing next generation IVD's for bloodstream infections. This role will be a hybrid role and will play an important part in making sure their products meet quality and regulatory compliance.
What you'll be doing?
You will be working with the wider team to implement a QMS that meets ISO 13495 requirements, maintain and improve the QMS through product development, and prepare for ISO accreditation. You will also be involved in regulatory submissions and addressing regulatory requirements for the products.
What they are looking for?
They are looking for someone who has a strong background in quality and regulatory management within the biotech or medical industry as well as an in-depth knowledge of ISO 13485.
What you'll get in return for your experience?
The salary on this role is up to £65,000 based in Bristol.
What's next?
If this role sounds like something you would be interested in then please apply through the job advert or drop me an email on .