RA/QA Consultant - Perm - Home based

Regulatory Affairs - Devices - RA/QA
Ref: 19 Date Posted: Thursday 12 Sep 2019
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RA/QA Specialist – Medical Devices - Home Based


Our client is a small, growing specialist Medical Device Consultancy. Due to continued growth, they have created a new vacancy for a RA/QA Specialist to work in a home-based role supporting a range of medical device clients.


Activities will include CE marking, Quality System management / support, global product registrations, MDR transition, QA/RA training.


This is an excellent opportunity to join a small, growing consultancy with excellent exposure to a various projects with a range of medical device clients.  


Please apply today or contact Josh Craven at Indo Professionals for more detail. 01256 597 800 / josh@indoprofessionals.co.uk


Job reference:




Up to circa £55,000 per annum (depending on experience) plus benefits. Applicants seeking more or less will also be considered



Home based – can be based anywhere in UK



RA/QA Specialist / Consultant – perm


Experience required:

Our client is looking for professionals with strong medical device regulatory & quality experience, they can consider applicants seeking a step up into a senior level role or in a supporting role or someone who can work in a standalone role at a senior level. The ideal applicant will meet a good percentage of the following experience requirements:

  • Clinical evaluation reporting
  • CE marking
  • Global registrations  
  • MDR transition
  • QA/RA training
  • Degree level education – or relevant working experience
  • Excellent communication, presentation skills
  • Full UK driving license – must


Job role:

Within this role the successful RA/QA Specialist will be working within the technical, regulatory and quality teams of the client to provide consultancy services. Projects may involve;

  • Set up of technical documentation & design dossiers – supporting CE marking and 510Ks
  • Conduct or advise on design / product risk management activities
  • Conduct or advise on post market surveillance and vigilance
  • Support to maintain or expand market access to various markets including EU, USA
  • Conduct or advise on validation projects
  • Management of quality systems


Indo Professionals is a specialist medical device staffing business focused on placing high calibre professionals into regulatory affairs, quality assurance and clinical research positions UK wide. If you are looking for a new career challenge or would like a career consultation with an industry expert, please contact the team today.