RA Director

Posted 13 December 2022
Salary Competitive
Job type Permanent
Contact NameLouise Cleland

Job description

The Role

  • Manage all regulatory aspects of the full product lifecycle
  • International product registrations, including leading FDA 510k submissions
  • Regulatory point of contact for all competent authorities
  • Responsible for regulatory strategy & technical documentation



  • Degree in life sciences or related field
  • Approximately 10 years' regulatory affairs experience in the medical device industry
  • Strong FDA, ISO13485 & AIMD experience
  • Previous leadership experience


If you are interested in this position, please apply within or email me on louise.cleland@biotalent.com with the job title and location of the role in the subject line.