Junior International Regulatory Specialist
Pubblicato il 16-10-2026 - Orthofix Holdings in Bussolengo
Why Orthofix? Guided by our organizational values – Take Ownership | Innovate Boldly | Win Together – we collaborate closely with world‐class surgeons and other partners to improve people's quality of life. At Orthofix, we want team members who build relationships and share knowledge, challenge the status quo, and deliver results every day to help us achieve our vision to be the unrivaled partner in Med Tech. Our global team of over 1,600 employees brings to market highly innovative, cost‐effective, and user‐friendly medical technologies that heal musculoskeletal pathologies for patients and the healthcare professionals who treat them. Looking to change people's lives? Look no further. We are looking for a Junior International Regulatory Specialist to join our Regulatory Affairs team, based in Bussolengo (Verona) on a maternity substitution contract. You will report to the Regulatory Affairs Manager. You will collaborate with Regulatory International area and RA Administrative specialist to assure International Product/facility(ies)
application submissions including international registrations and/or license applications, are up to date in compliance to the international regulatory requirements and in time with requested deadline.
Responsibilities include collaboration with all internal departments, consultants, subsidiaries, distributors, external laboratories and suppliers for successful regulatory activities in each impacted area.
What will your contribution be? Assures, that the Regulatory International documentation on paper or on electronic relevant to a new or modified products is adequately updated for International Products applications.
Provide in timely manner any regulatory product registration/submission information status to able to update the Regulatory file platform /data on time.
Prepare and maintain updated Procedure Pack Files.
As needed, support the Regulatory team in the daily regulatory activities, as indicated by the Regulatory manager
Prepare