Robert Miller

Quality Consultant

I have been in the medical device industry/IVD industry for the last 9 years. I started as a Junior
Quality Engineer working for a large kit packing company. I have since then progressed to QA/RA
manager for a medium size medical device company, and then most recently I became a consultant.
It is an exciting time for the industry with many changes and challenges regarding how the industry
operates, and the new requirements imposed by Brexit and the MDR. I am passionate about creating
quality systems that deliver the best patient outcomes and allow for a pragmatic, sustainable quality
first approach. In recent years I have been involved in building CAPA systems, PMS systems, audit
programmes, providing inputs for MDR tech files, building rework systems and anything else the
industry requires as the regulatory framework evolves.
I am a qualified lead auditor and have a real desire to help people minimise their business risk and put the patient first. Working at Advena UK is really giving me a platform to utilise these skills and provide the best possible advice to clients.

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