Vice President Regulatory Affairs

ARTO; Bristol; On-site; GBP 80,000 - 120,000; Full time

Job summary

An innovative Bio-MedTech company in Bristol is hiring a VP of Regulatory Affairs to shape the global regulatory strategy for its expansion. The ideal candidate will have a strong background in biologics and advanced wellness focused on navigating regulatory paths across the UK, EU, and US. Responsibilities include leading scientific dialogue with regulators, defining compliance strategies, and building internal regulatory frameworks. This role is perfect for a senior regulatory leader eager to thrive in a fast-paced environment pushing the boundaries of health and longevity.

Qualifications

• UK-based senior regulatory leader with experience in biologics and advanced wellness technologies.
• Strong track record of leading regulatory strategy and early regulatory dialogue.
• Pragmatic, solutions-focused individual who thrives in dynamic environments.

Responsibilities

• Define the global regulatory roadmap across multiple jurisdictions.
• Clarify classifications and claims for novel biologics and digital innovations.
• Lead scientific dialogue with major regulators like MHRA and FDA.
• Build internal regulatory and quality documentation standards.
• Guide partnerships and clinical deployments to ensure compliance.

Skills

Leadership in regulatory strategy

Experience with biologics

Regenerative medicine knowledge

Understanding of regulatory frameworks

Solutions-focused approach

Job description

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
• Someone pragmatic, solutions-focused, and comfortable building from scratch in a dynamic environment
• A strong track record leading regulatory strategy, innovation pathways, or early regulatory dialogue

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

[e-mail]