Barrington James are exited to post a fantastic opportunity for one of our close clients. This company is a Medical Device manufacturer. They are backed by some serious investors the industry and are looking for future support within their regulatory. This opportunity is perfect for someone who is ambitious, independent and wants to play a key role in working on the most innovative projects.
Key Responsibilities
* Class I medical devices, ensuring adherence to UKCA and CE marking requirements, as well as compliance with UK MDR and ISO 13485 standards. Acting as the organisation’s regulatory lead, you will work cross‑functionally with teams including Quality, R&D, and Operations, as well as external partners, to support product development, maintain compliant documentation, and enable efficient market access.
This truly is an exiting opportunity for someone to join an ambitious company who are continuing to impress the market with their ground‑breaking studies.
The opportunity has understandably been incredibly popular. We encourage all interested candidates to apply immediately as it is likely that recruitment will close prematurely.
By clicking "apply" you will be sending your CV to Isobella Mcpherson at Barrington James. Isobella is a specialist Medical Device, engineering recruiter and will discuss the opportunity in detail with you, facilitate your application and will manage the process acting as a link between the company and yourself.
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