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Regulatory Affairs Specialist

1 month ago

London, Greater London, United Kingdom Athsai Full time
Job Title: Regulatory Affairs Specialist - Precision Medicine

Join Athsai as a Regulatory Affairs Specialist - Precision Medicine and contribute to the development of innovative medical devices. In this role, you will work closely with cross-functional teams to ensure compliance with regulatory requirements and develop strategies for global regulatory submissions.

Key Responsibilities:

  • Develop and implement regulatory strategies for precision medicine devices
  • Collaborate with clinical teams to ensure regulatory compliance in clinical trials
  • Lead global regulatory submissions and interact with health authorities
  • Contribute to the development of regulatory strategies for digital health products

Requirements:

  • Bachelor's degree in a relevant field; advanced degree preferred
  • 5+ years of experience in medical device regulatory affairs
  • 4+ years of experience in US Medical Device Regulatory Affairs

About Athsai:

Athsai is a leading pharmaceutical company dedicated to developing innovative treatments for various diseases. We are committed to excellence and strive to make a positive impact on people's lives.