Vice President Regulatory Affairs

ARTO; Birmingham; On-site; GBP 90,000 - 130,000; Full time

Job summary

A leading Bio-MedTech firm is seeking a VP of Regulatory Affairs to shape global regulatory strategies in a pioneering environment. The ideal candidate will have a strong background in biologics or comparable technologies and a proven track record in regulatory leadership. Responsibilities include defining the regulatory roadmap across multiple jurisdictions and engaging with major health authorities. This position offers an incredible opportunity to innovate in health and wellness, driving advancements globally.

Qualifications

• UK-based senior regulatory leader with a strong background in biologics or ATMPs.
• Experience with medical, biological, and wellness classifications.
• Proven track record in leading regulatory strategy and innovation pathways.

Responsibilities

• Own and define the global regulatory roadmap across multiple jurisdictions.
• Lead scientific dialogue with regulators including MHRA, EMA, and FDA.
• Build internal regulatory frameworks, quality structures, and documentation standards.

Skills

Regulatory strategy

Solutions-focused

Leadership

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]