Quality Regulatory Specialist

Posted 21 March by Adecco
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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.
With a heavier focus on RA, this is a role that will allow you to work on a variety of tasks throughout your career.

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.

You will work closely with the QARA Manager, and your role will grow as the company continue to expand their product portfolio.

Interested? Apply now with an up to date CV and I will be in touch.

Required skills

  • Regulatory
  • MDR
  • Technical Files
  • Medical Device

Reference: 52354907

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