Job Description

We are currently searching for a Quality professional who has a strong understanding of the vascular market. The role will be responsible for building, controlling and managing a portfolio of medical device schemes to deliver technical reviews, scheme management and Quality Management Systems Assessments in support of the CE marking process.

The role in its entirety will be this organisations vascular expert responsible for providing quality and regulatory guidance on all premarket activity from design through registration.

If you are degree educated in a relevant subject to medical devices, have a strong understanding of the design and development process of vascular products and a strong regulatory knowledge this is an excellent opportunity to join a rapidly expanding organisation that can offer solid career development opportunities.

 
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