UK Regulatory Affairs Lead — MAA Submissions & Strategy

Novo Nordisk; Gatwick; On-site; GBP 60,000 - 80,000; Full time

Job summary

A global healthcare company is seeking a Regulatory Affairs Lead in Gatwick, UK. This role involves managing and executing regulatory projects, providing strategic support, and collaborating across functions to align regulatory submissions with business needs. Candidates should have at least 8-10 years of experience in a regulatory environment, possess extensive knowledge of UK and EU legislation, and demonstrate strong stakeholder management skills. The position offers the opportunity to make a direct impact on patient health while working in a collaborative team environment.

Qualifications

• Minimum 8-10 years relevant Regulatory experience.
• Experience managing critical regulatory projects and submissions.
• Ability to interpret legislation and assess business impact.

Responsibilities

• Lead regulatory projects end to end, including resource planning.
• Compile and ensure submission of national MAAs and regulatory applications.
• Maintain regulatory intelligence on UK and EU legislation.

Skills

Pharmaceutical industry experience

Regulatory legislation knowledge

Stakeholder management

Microsoft systems proficiency

Problem-solving skills

Fluent English

Education

Science graduate or equivalent

Job description

A global healthcare company is seeking a Regulatory Affairs Lead in Gatwick, UK. This role involves managing and executing regulatory projects, providing strategic support, and collaborating across functions to align regulatory submissions with business needs. Candidates should have at least 8-10 years of experience in a regulatory environment, possess extensive knowledge of UK and EU legislation, and demonstrate strong stakeholder management skills. The position offers the opportunity to make a direct impact on patient health while working in a collaborative team environment.