EMEA Regulatory Lead & UKI Cluster Director

Santen; Greater London; On-site; GBP 125,000 - 150,000; Full time

Job summary

A global pharmaceutical company is seeking an experienced EMEA Regional Regulatory Lead to drive regulatory strategies across Europe, the Middle East, and Africa. In this role, you will manage all regulatory affairs activities for the UK & Ireland and lead multi-regional product strategies. Qualified candidates must have a minimum of 8 years of experience in regulatory affairs, particularly with MHRA and HPRA, and possess strong communication and collaboration skills. This full-time role requires no remote work and offers an inclusive work environment.

Qualifications

• At least 8 years of experience in medicinal Regulatory Affairs within Europe and the UK.
• Strong expertise navigating EMEA regulatory agencies.
• Proven experience designing regulatory strategies for development assets.
• Deep knowledge of medicinal legislation and regulatory guidelines.

Responsibilities

• Lead the development and implementation of EMEA regulatory strategies.
• Act as the EMEA representative within Global Regulatory Sub-Teams.
• Take ownership of regulatory strategy for products without a Global Regulatory Lead.
• Manage all affiliate-level Regulatory Affairs activities for the UK & Ireland.

Skills

Regulatory submissions

Strong expertise with MHRA and HPRA

Communication skills in English

Collaboration abilities

Job description

A global pharmaceutical company is seeking an experienced EMEA Regional Regulatory Lead to drive regulatory strategies across Europe, the Middle East, and Africa. In this role, you will manage all regulatory affairs activities for the UK & Ireland and lead multi-regional product strategies. Qualified candidates must have a minimum of 8 years of experience in regulatory affairs, particularly with MHRA and HPRA, and possess strong communication and collaboration skills. This full-time role requires no remote work and offers an inclusive work environment.