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Regulatory Affairs Specialist

2 months ago

Oxford, Oxfordshire, United Kingdom Cure Talent Full time
Regulatory Affairs Associate Opportunity

Cure Talent is excited to partner with a leading Medical Devices Manufacturer to find an experienced Regulatory Affairs Associate to join their team.

This is a hybrid role with regular site visits, requiring a strong understanding of global regulatory frameworks and expertise in MDR, particularly for Class III devices.

Key Responsibilities:
  • Support global product registrations and maintain design dossiers
  • Ensure compliance with international regulatory requirements
  • Coordinate worldwide product registration submissions and ongoing maintenance
  • Support regulatory activities related to change note approvals and complaint file reviews
  • Assist in delivering new and existing products in compliance with global regulatory standards

We are seeking an experienced regulatory professional with a proven track record in Medical Devices and a strong understanding of global regulatory frameworks.

Requirements:
  • Proven experience in a Regulatory Affairs role in Medical Devices
  • Knowledge and experience of Class III Medical Devices
  • Knowledge of Product Registrations, preferably Worldwide

If you have the necessary skills and experience to succeed in this role, please get in touch with the team at Cure Talent today.