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

Requirements

• 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.