Vice President Regulatory Affairs

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

Job summary

An innovative Bio-MedTech company in the UK is seeking a VP of Regulatory Affairs to define and lead their global regulatory strategy. The role involves overseeing the roadmap across various jurisdictions and engaging with multiple regulators like MHRA and FDA. Ideal candidates should have strong background in biologics and ATMPs with proven leadership in regulatory strategy. This role offers the chance to shape compliance in a fast-growing environment focused on advancing human health.

Qualifications

• Proven experience as a senior regulatory leader based in the UK.
• Background in biologics, ATMPs, regenerative medicine or advanced wellness.
• Track record of innovative regulatory strategy development.

Responsibilities

• Define the global regulatory roadmap across multiple jurisdictions.
• Clarify classifications and compliant claims for diverse health technologies.
• Lead dialogue with regulators including MHRA, EMA, and FDA.

Skills

Regulatory strategy development

Experience with biologics and ATMPs

Pragmatic problem solving

Strong communication skills

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]