At a Glance
- Tasks: Lead regulatory strategies for medical devices and manage lifecycle activities.
- Company: Join Perrigo, a leader in healthcare innovation.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborative culture with a focus on continuous improvement and digital enablement.
- Why this job: Make a real impact on consumer safety and market access in a dynamic environment.
- Qualifications: Experience in regulatory affairs and strong leadership skills required.
The predicted salary is between 60000 - 80000 £ per year.
Description Overview We are excited to recruit a Senior Manager Regulatory Affairs Lifecycle Management Medical Devices.
This is a newly created role within Perrigo's Scientific Office.
As Medical devices Lead for LCM you will play a key role in delivering Perrigo’s regulatory strategy across the product lifecycle.
You will support the development and execution of regulatory strategies, ensuring the consistent delivery of high-quality regulatory outcomes across a diverse and complex portfolio.
You will be responsible for managing lifecycle management activities, overseeing the preparation, submission, and maintenance of regulatory dossiers in line with global requirements and business priorities.
You will proactively identify risks, support mitigation planning, and ensure timely, compliant submissions that help maintain supply continuity, consumer safety, and market access.
Leading a team of multi-regional regulatory professionals, you will provide clear direction, support capability development, and foster a culture of accountability and continuous improvement.
You will manage priorities across multiple activities, ensuring effective execution and alignment with departmental and organisational goals.
Working closely with cross-functional stakeholders—including Quality, Safety, Supply Chain, and R approve submission readiness and escalate novel or high-risk issues and major supply or portfolio risks.
Drive process simplification, digital enablement, and continuous improvement across lifecycle and operational delivery.
Ensure disciplined handovers between Category, Cluster, and LCM/Ops and maintain One Regulatory Voice and implementation tracking.
Leadership people leadership experience preferred.
Strong regulatory writing, stakeholder management, and operational delivery leadership.
Demonstrated areas of expertise Regulatory Expertise
