At a Glance
- Tasks: Lead regulatory lifecycle management for medicines and shape global strategies.
- Company: Perrigo, a leading company in the healthcare sector.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Join a high-performing team and drive transformation in a dynamic environment.
- Why this job: Make a real impact on global healthcare by ensuring market access for vital medicines.
- Qualifications: Experience in regulatory affairs and strong leadership skills.
The predicted salary is between 80000 - 120000 £ per year.
Perrigo in the United Kingdom is recruiting a Director - Regulatory Affairs Lifecycle Management Medicines to lead the lifecycle management for medicines, shaping global regulatory strategies and ensuring timely, compliant submissions that protect supply continuity and enable market access.
You will lead a high-performing team, collaborating with Quality, Safety, Supply Chain and R&D to drive transformation and implement an enterprise operating model for post-approval activities across markets.
Director, Regulatory Lifecycle – Medicines (Hybrid) in England employer: Perrigo
Perrigo is an exceptional employer located in the vibrant city of London, offering a dynamic work culture that fosters collaboration and innovation. As a leader in regulatory affairs, you will have the opportunity to drive impactful change while working alongside talented professionals in Quality, Safety, Supply Chain, and R&D. With a strong focus on employee growth and development, Perrigo provides ample opportunities for career advancement and the chance to contribute to ongoing consumer safety and product excellence.
