Regulatory Affairs Specialist - Cheshire, United Kingdom - Cast UK Limited

Cast UK Limited
Cast UK Limited
Verified Company
Cheshire, United Kingdom

3 weeks ago

Tom O´Connor

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Tom O´Connor

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Description
**Regulatory Affairs Specialist
Cheshire
£ Competitive Salary**
Role Profile
Our client is a highly successful medical device business based in Cheshire.

They are currently looking to appoint a Regulatory Affairs Specialist to provide regulatory expertise in the business research, development and marketing of products.


The key purpose of the role will be to prepare regulatory submissions to ensure that regulatory approvals are achieved and retained within ongoing projects and needs of the business.


Key responsibilities will include:


  • Provide continuous regulatory advice by participating in ongoing projects
  • Support the delivery of global regulatory programmes
  • Create, maintain and review ongoing projects and advise on its compliance with regulations
  • Maintain uptodate knowledge of regulatory legislation and guidelines

Skills and Experience

  • Higher degree in medical, biological or chemical sciences preferred
  • Atleast 2 years' experience in Medical Device Regulatory Affairs, Post Market Surveillance, Quality Assurance, Design Control or related function
  • Experience of Medical Device registration in global markets

Client
Our client is a highly successful medical device business based in Cheshire. The business has continued to see growth year on year and is a key player in its market.

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