Global Regulatory Affairs VP: Lead Strategy & Inspections

Tokamak energy; Cherwell District; On-site; GBP 90,000 - 130,000; Full time

Job summary

A leading Cell and Gene Therapy CDMO is seeking a VP, Global Regulatory Affairs to provide regulatory leadership for advanced therapy programmes. In this role, you will develop global regulatory strategies and act as a senior representative with health authorities. You will lead and mentor a global regulatory team while fostering client partnerships and ensuring compliance throughout the product lifecycle. This position offers visibility at the executive level and the chance to influence regulatory strategies in a rapidly evolving field.

Qualifications

• Extensive experience in global regulatory affairs within biologics or advanced therapy.
• Proven leadership experience managing regulatory teams.
• Ability to lead strategic regulatory initiatives ensuring compliance.

Responsibilities

• Develop and execute global regulatory strategies for client programmes.
• Act as senior regulatory representative with global health authorities.
• Provide regulatory input across CMC, clinical, and post-approval activities.
• Lead a global regulatory team, fostering collaboration and professional development.

Skills

Global regulatory leadership

Strong partnerships with regulatory authorities

Team leadership and coaching

Education

Degree in Pharmaceutical chemistry, biochemistry, or regulatory science

Job description

A leading Cell and Gene Therapy CDMO is seeking a VP, Global Regulatory Affairs to provide regulatory leadership for advanced therapy programmes. In this role, you will develop global regulatory strategies and act as a senior representative with health authorities. You will lead and mentor a global regulatory team while fostering client partnerships and ensuring compliance throughout the product lifecycle. This position offers visibility at the executive level and the chance to influence regulatory strategies in a rapidly evolving field.