Toby Shelton

Background and expertise
Known for his consultative approach and deep understanding of the regulatory landscape, Toby partners with high-growth MedTech companies to connect them with professionals who ensure products meet the highest standards of safety, compliance and innovation.

With a strong understanding of ISO 13485, MDR, FDA 21 CFR Part 820 and other global regulatory frameworks, Toby brings more than recruitment expertise. He provides valuable market insight into the evolving demands of the industry, helping organisations secure the talent needed to achieve their growth and regulatory objectives. Whether sourcing Quality Assurance leaders for scaling businesses or placing specialists within notified bodies, Toby is trusted to deliver candidates who align with both technical requirements and company culture.

His network spans start-ups, SMEs and global medical device manufacturers, and he is particularly experienced in supporting organisations navigating regulatory change, market expansion and key product development milestones.

Events and external appearances
Toby attended MEDICA in Düsseldorf, Germany, one of the world’s leading healthcare and MedTech trade exhibitions. The event provided an opportunity to connect with innovators, industry leaders, investors and emerging companies while gaining insight into the latest trends and technologies shaping the future of healthcare.

He has also been involved in R&D Partners’ exclusive MedTech Investor Networking Event, which brought together innovative MedTech founders and leading investors from across the sector. The event facilitated meaningful discussions, knowledge sharing and strategic connections to support growth and innovation within the MedTech ecosystem.

Hear from Toby
“Driven by curiosity and a genuine interest in medical innovation, I see recruitment as a way to accelerate progress in healthcare. I’m not just filling roles; I’m helping build the teams that bring life-changing technologies to market.”