Regulatory Affairs Specialist - Medical Devices UK/IE

Regulatory Affairs Specialist - Medical Devices UK/IE

  • Location

    London, England

  • Sector:

    Regulatory Affairs

  • Job type:


  • Salary:


  • Contact:

    Matt Thomas

  • Contact email:


  • Job ref:


  • Published:

    7 months ago

  • Expiry date:


  • Consultant:


Job title: Regulatory Affairs Specialist - Medical Devices UK/IE

A Pharmaceutical business in London are seeking an individual with extensive Medical Device and Medicines experience to join their Regulatory Affairs. In this role you will be responsible for maintaining marketing authorisations, assists in new MAAs and provide life cycle maintenance for various products.


  • Life Cycle Maintenance for existing products within the UK and Ireland (National, MRP and DCP)
  • Support Module 1 documents for new MAAs for both the UK and Ireland markets
  • Prepare, submit and manage applications with the MHRA and HPRA
  • Undertake 'ad-hoc' duties such as pharmacovigilance, labelling, artwork etc…
  • Maintain collaboration with EMEA counterparts


  • Minimum of 2 years' experience within Regulatory Affairs
  • Experience in Medical Devices is essential
  • Degree level educated within life sciences
  • Experience working within UK/IE markets (MHRA and HPRA)
  • Experience across National, MRP and DCP

Salary and benefits:

A competitive salary, annual bonus and wider benefits scheme is on offer

To apply for this position or hear further details then please contact Matt Thomas via matt.thomas@pharma-partners.co.uk