Vice President Regulatory Affairs

ARTO; Manchester; On-site; GBP 90,000 - 120,000; Full time

Job summary

An innovative Bio-MedTech company is seeking a VP of Regulatory Affairs to shape the global regulatory strategy. This senior role is ideal for a leader with experience in biologics and advanced wellness, capable of navigating multiple jurisdictions including the UK and EU. Responsibilities include defining the regulatory roadmap, engaging with regulators, and building quality frameworks. The role offers the opportunity to drive pioneering projects in a dynamic health-focused environment.

Qualifications

• Senior regulatory leader based in the UK.
• Experience in biologics, ATMPs, or novel health technologies.
• Proven track record in regulatory strategy and innovation.

Responsibilities

• Define the global regulatory roadmap across multiple jurisdictions.
• Lead early scientific dialogue with regulators.
• Build internal regulatory frameworks and quality structures.

Skills

Leadership in regulatory affairs

Experience with biologics

Background in advanced wellness

Pragmatic and solutions-focused mindset

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]