Regulatory Affairs
1 month ago
Adecco are working with a Medical Device company focused on rapid growth over the next two years.
Our client, a supplier of Class I Medical Devices, is looking for a permanent QARA Specialist to join the team.
Based in Northampton, the client is happy to allow hybrid working with 2 days from home and 3 days in the office.
There are two main projects to focus on initially:
Creating technical files for the company's products, collaborating with external regulatory consultants for gap analysis and review.
Managing and reporting on complaints, conducting thorough investigations, and ensuring timely resolution.
Working for a smaller organisation like this, it's important you are used to a busy manufacturing environment, with the ability to explain complicated QARA processes in simple terms to the wider business.
