We are excited to recruit an Associate Professional, Regulatory Affairs within our Medical Device Lifecycle Management team. In this role,you will play an important role in supporting Perrigo's medical device portfolio throughout the product lifecycle. You will contribute to regulatory activities that help maintain ongoing conformity, technical documentation compliance, product availability and market access across multiple regions and markets.
You will support lifecycle management activities including technical documentation updates, change assessments, regulatory notifications, registrations/listings and maintenance of regulatory records in accordance with applicable medical device requirements, approved procedures and business priorities. Working alongside experienced regulatory professionals, you will help ensure documentation remains current, traceable and inspection-ready, and that regulatory deliverables are completed to agreed timelines.
You will manage a range of defined regulatory activities and support change control, product maintenance, labelling updates, technical file remediation and ongoing compliance obligations. You will help identify potential regulatory issues, support risk mitigation activities and contribute to the successful delivery of medical device lifecycle objectives.
Working closely with cross-functional stakeholders including Quality, Safety, Supply Chain, Manufacturing, R&D, Packaging/Artwork, you will provide regulatory support for product and process changes and assist in translating medical device regulatory requirements into practical actions that support compliance and business needs.
You will contribute to the continuous improvement of Medical Device Regulatory Affairs processes, systems and ways of working, helping to improve efficiency, consistency, data quality and inspection readiness across lifecycle activities. Through your role, you will build regulatory expertise in medical devices while supporting Perrigo's commitment to maintaining high standards of compliance, consumer safety and product quality.
This role offers an excellent opportunity to develop a strong foundation in Medical Device Regulatory Affairs, gain experience across the product lifecycle and build both technical and professional capabilities within a dynamic global environment.
