Vice President Regulatory Affairs in Cambridge

We are supporting an innovative Bio–MedTech company operating at the intersection of advanced therapies, biologics, wellness, and digital health and they are now hiring a VP of Regulatory Affairs.

The role will be required to shape the global regulatory strategy for a fast-growing Bio-MedTech expanding across the UK, EU/Switzerland, US, Middle East and Asia. The role is ideal for a senior regulatory leader who thrives in a pioneering, fast-moving environment and wants to be part of a mission pushing the boundaries of human health and longevity.

Key Responsibilities:

• Own and define the global regulatory roadmap across multiple jurisdictions
• Clarify classifications and compliant claims for novel biologics, ATMPs, wellness interventions and digital innovations
• Lead early scientific dialogue with regulators (MHRA, EMA, Swissmedic, FDA and others)
• Build the internal regulatory frameworks, quality structures and documentation standards
• Guide communications, partnerships, and clinical/wellness deployments to remain compliant

Qualifications:

• UK-based senior regulatory leader
• Background in biologics, ATMPs, regenerative medicine, advanced wellness, or novel health technologies
• Experience working on boundaries between medical, biological and wellness classifications
• A strong track record leading regulatory strategy, innovation pathways, or early regulatory dialogue
• Someone pragmatic, solutions-focused, and comfortable building from scratch in a dynamic environment

If your interested, or know someone who might be, reach out to me at:

felix.chennery@arto-talent.com