Regulatory Affairs Specialist
Who We Are at Drive DeVilbiss
Drive DeVilbiss has become a leading manufacturer of medical products with a strong and consistent track record of growth achieved both organically and through acquisitions. We are proud of our high-quality, diverse product portfolio, channel footprint and global operating scale. Our products are sold into the homecare, long-term care, retail, and e-commerce channels in more than 100 countries around the world.
Leading the World with Innovative Healthcare Solutions that Enhance Lives
Were looking for a Regulatory Affairs Specialist to join our team. In this role, youll ensure our medical devices meet UK, EU, and international regulatory standards, with fully compliant technical documentation. Youll work closely with cross-functional teams including design, quality, and other regulatory professionals, taking ownership of your workload and driving continuous improvement.
Key Responsibilities:
* Create and review technical files in line with EU MDR and other global regulations
* Develop supporting documentation including risk management, usability, and clinical evaluation reports
* Provide expert regulatory support to internal and external stakeholders
* Maintain high standards of confidentiality and departmental organisation
What Youll Bring: