Medicines Lifecycle Regulatory Lead

Perrigo; Greater London; Hybrid; GBP 110,000 - 170,000; Full time

Job summary

Perrigo in London, United Kingdom, seeks a Manager for Regulatory Affairs Lifecycle Management to lead medicines post-launch strategy and regulatory submissions. You will guide multi-regional teams, ensure timely changes, and coordinate with Quality, Supply Chain and R&D to maintain compliance and market access.

This hybrid role offers leadership development, regulatory process improvements, and accountability for portfolio regulatory outcomes in a dynamic global environment.

Qualifications

• Typically 8–10+ years in Regulatory Affairs with medicines lifecycle or post-launch compliance expertise.
• Experience leading cross-functional teams and managing competing priorities.
• Strong regulatory writing and stakeholder management in a matrix organization.

Responsibilities

• Lead post-launch regulatory strategy and compliance for the medicines portfolio.
• Oversee lifecycle submissions, variations, renewals and reporting activities.
• Manage a multi-regional team and align governance across functions.

Skills

Regulatory Affairs

Leadership

Regulatory writing

Stakeholder management

Cross-functional collaboration

Education

Scientific or technical degree

Job description

Perrigo in London, United Kingdom, seeks a Manager for Regulatory Affairs Lifecycle Management to lead medicines post-launch strategy and regulatory submissions. You will guide multi-regional teams, ensure timely changes, and coordinate with Quality, Supply Chain and R&D to maintain compliance and market access.

This hybrid role offers leadership development, regulatory process improvements, and accountability for portfolio regulatory outcomes in a dynamic global environment.