Were Hiring: Regulatory Affairs Division Leader – Diagnostics | Edinburgh (Hybrid) A global diagnostics innovator is entering a major growth phase, and we’re searching for a proven Regulatory Affairs Leader to steer them through it. Backed by significant investment and driving into the US market with FDA submissions, this company is scaling up fast, launching new products, expanding manufacturing, and assembling a US commercial team. Your Mission: Lead the regulatory function across global markets, oversee compliance, and drive strategy. You’ll be the go-to expert guiding the business through complex regulatory landscapes, from ISO13485 to FDA and IVDR. What You’ll Be Doing: Owning global RA strategy and leading from the front Overseeing regulatory submissions: CE marking (IVDD/IVDR), FDA, Health Canada Ensuring company-wide compliance and audit readiness Leading your team and partnering with senior cross-functional stakeholders Contributing to quality initiatives and post-market surveillance Navigating evolving international legislation and regulatory requirements What You’ll Bring: ✅ Experience in diagnostics or medical device manufacturing ✅ Strong track record with FDA, CE marking, IVDR, and ISO13485 ✅ Leadership and strategic influence in regulatory functions ✅ A sharp, decisive, and collaborative mindset Why Join? Global impact, major growth runway State-of-the-art facilities in Edinburgh Collaborative, people-first culture with regular team incentives Opportunities for international secondments and long-term progression