Director - Regulatory Affairs Lifecycle Management Medicines

Director - Regulatory Affairs Lifecycle Management Medicines

Full-Time 80000 - 120000 £ / year (est.) No working from home possible
Perrigo Company plc

At a Glance

  • Tasks: Lead regulatory strategy for medicines, ensuring compliance and high-quality outcomes.
  • Company: Join Perrigo, a top player in the European Consumer Self-Care market.
  • Benefits: Inclusive culture, career growth, and the chance to make a real impact.
  • Other info: Be part of a dynamic team driving innovation and consumer safety.
  • Why this job: Shape the future of health and wellness solutions that everyone trusts.
  • Qualifications: Advanced degree and significant experience in Regulatory Affairs leadership.

The predicted salary is between 80000 - 120000 £ per year.

At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All .

We are proud to be a top 10 player in the European Consumer Self‑Care market and the largest U.

S. store‑brand provider of over‑the‑counter and infant formula.

Dedicated to providing The Best Self‑Care for Everyone , we are the people behind the brands you trust – Opill®, Compeed®, Solpadeine®, Ni Quitin®, and many more.

We Are Perrigo.

We are committed to enhancing the wellbeing of our colleagues and consumers alike, and we pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.

Description Overview We are excited to recruit a Director – Regulatory Affairs Lifecycle Management Medicines.

This is a newly created role within Perrigo Scientific Office.

As the leader of Lifecycle Management for Medicines you will be a senior leader driving the delivery of Perrigo’s global regulatory strategy across the full product lifecycle.

You will shape and execute robust regulatory strategies, ensuring the consistent delivery of high‑quality regulatory outcomes across a diverse and complex portfolio.

You will hold end‑to‑end accountability for lifecycle management activities, overseeing the development, submission, and maintenance of regulatory dossiers to meet global requirements and business priorities.

Through strong leadership and decision‑making, you will anticipate risks, define mitigation strategies, and ensure timely, compliant submissions that protect supply continuity, consumer safety, and enable market access.

Leading a high‑performing team, you will set clear direction, build capability, and foster a culture of ownership, accountability, and continuous improvement.

You will ensure effective prioritisation and execution across competing demands, aligning regulatory activities with broader organisational objectives.

As a key partner to cross‑functional stakeholders – including Quality, Safety, Supply Chain and R operating with enterprise‑scale complexity and accountability through leaders and specialist teams.

Capability Leadership advanced degree preferred.

Significant experience in a progressive Regulatory Affairs leadership across portfolios, regions, or capabilities.

Proven leadership in enterprise portfolio delivery, governance ownership, operating model design, and transformation.

  • Demonstrated areas of expertise
  • Enterprise

Leadership: Sets direction, aligns stakeholders, and delivers outcomes through leaders and teams.

Strategic

Foresight: Anticipates regulatory trends and builds proactive plans and policy positions where appropriate.

Governance

Perrigo Company plc

Contact Details:

Perrigo Company plc Recruitment Team

We think you need these skills to ace Director - Regulatory Affairs Lifecycle Management Medicines

Regulatory Strategy Development
Lifecycle Management
Regulatory Dossier Submission
Risk Anticipation and Mitigation
Leadership and Team Management
Cross-Functional Collaboration
Governance Ownership