We are excited to recruit a Regulatory Affairs Professional to join the Non-Medicinal Lifecycle Management team. In this role, you will play an important role in supporting Perrigo's non medicinal portfolio including cosmetics, VMS, general products and other non-medicinal classifications such as medical devices across the product lifecycle. You will contribute to the development and execution of regulatory strategies, helping to deliver high-quality regulatory outcomes across a diverse and dynamic portfolio.
You will be responsible for managing lifecycle management activities, including the preparation, maintenance and delivery of regulatory documentation, product information files, technical files, notifications, registrations and supporting records in line with global requirements and business priorities. You will identify regulatory risks, support mitigation activities, and ensure timely, compliant regulatory filings and documentation updates that help maintain supply continuity, consumer safety and market access.
Working both independently and collaboratively, you will manage priorities across multiple activities and projects, ensuring effective delivery and alignment with departmental objectives. You will develop strong partnerships with colleagues across Regulatory Affairs and the wider business to support successful execution of lifecycle initiatives.
Working closely with cross-functional stakeholders, including Quality, Safety, Supply Chain and R&D, you will provide regulatory input to change management activities and business initiatives. You will help translate regulatory requirements into practical actions that support product maintenance, compliance and portfolio optimisation.
You will also contribute to the continuous improvement of Regulatory Affairs processes and ways of working, helping to drive greater efficiency, consistency and effectiveness across lifecycle activities. Through your role, you will support Perrigo's ability to meet evolving regulatory requirements while maintaining high standards of compliance and quality.
This role offers the opportunity to make a meaningful contribution within the Regulatory Affairs organisation, supporting product availability and regulatory performance while further developing your regulatory expertise, business knowledge and professional capabilities in a dynamic global environment.
