Stories and Viewpoints

Brian Callaghan: Roles in quality have become ‘much more specialised’ in medtech

Medtech professional Brian Callaghan shares his experience of the industry and how it has changed over the past decade.


Brian Callaghan has been working in the medtech industry for 16 years across a range of roles in quality and compliance. He joined Viatris three years ago and now works as a senior manager in device development assurance.


In his role, Callaghan predominantly works on quality system and compliance-related projects, updating procedures and processes to meet the requirements of new and updated standards and regulations.


He’s also responsible for executing product lifecycle management projects and tasks, such as integrating acquired product documentation into the quality management system and executing reviews of marketed device combination product performance.



To explore R&D career opportunities with Viatris, click here.

Read the full feature article on Silicon Republic here

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