Consultant Medical Devices Regulatory Affairs

Job description

What you’ll do Qserve offers an exciting opportunity to join our team as a Consultant Medical Devices Regulatory Affairs. In this role, you will support clients in the medical device industry, with a strong focus on regulatory strategy, compliance, and market access. Leveraging your regulatory expertise, you will guide clients through complex global regulatory frameworks and help bring innovative medical devices to market efficiently and compliantly. You work closely with clients on a variety of regulatory topics, for example: Contributing to regulatory strategies for EU MDR and other global markets Preparing and reviewing technical documentation: Supporting market access activities and regulatory submissions Advising on regulatory requirements and classification Keeping up with regulatory developments and helping clients apply them in practice You’ll collaborate with colleagues and clients across different disciplines and countries, making sure projects move forward and regulatory requirements are met. Requirements: What you’ll bring to the team We are looking for a Regulatory Affairs professional with experience in medical devices and a strong interest in compliance and market ac...