Regulatory Affairs Consultant 

Location: Guildford

Contract: Full Time.

Industry: Pharmaceuticals

Salary: Competitive (dependent on experience).


  • Ensuring understanding of new regulatory and scientific developments.
  • Ensuring understanding of regulatory strategy and objectives.
  • Proffering authorization strategies and regulatory advice for clients.
  • Overseeing of compliance in line with ISO 13485 accreditation.
  • Responsible for regulatory projects and providing registration advice to in-house departments.
  • Actively supporting and training other team members in specialist skill areas.


  • BSc in a medical or paramedical or equivalent by experience (pharmacy, biology, etc).
  • Minimum of 3 years of experience in the pharmaceutical sector/medical device industry.
  • Experience in drug improvement and dissemination.
  • Experience with EU regulatory procedures governing product safety and stewardship.
  • Strong project management skills.
  • Flexible and positive work attitude.

I am looking forward to having a chat with you if you are suitable for this role. For more information on this exciting opportunity please email a copy of your CV in MS WORD format to using Regulatory Affairs Consultant as the Subject.

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Job Location: Guildford

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