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. 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. 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 UpToDate International data bases (e.g.



Support during the audit/inspection carried out by Notified Body or Competent Authorities for the facility’s certification What business skills are we looking for? Technical degree 1 years in similar position preferably in a Medical Device Company Good English and Italian, both written and oral Knowledge of medical device European MDR.

Japanese, Canadian, Latin America, Middle East, India,Asia-Pacific regulations, would be a plus. Technical knowledge of the medical devices and of the Company manufacturing processes Project management Able to work in team and autonomously as well Open mind to different culture Friendly, warm, and innovative atmosphere Healthy, inspiring, and international and inclusive work environment Training and development opportunities Wellbeing initiatives (welfare) Canteen Benefits (Pension Fund- Health Insurance etc..) 8:30-17:30 Monday to Thursday and 8:30-16:30 Friday. maternity substitution ~ Tempo pieno ~ Since 1980, Orthofix has evolved and grown to become one of the leading medical device companies with a spine and orthopedics focus in the world. Our newly merged Orthofix-SeaSpine organization is a leading global spine and orthopedics company with a comprehensive portfolio of biologics, innovative spinal hardware, bone growth therapies, specialized orthopedic solutions, and a leading surgical navigation system.

Our products are distributed in 68 countries worldwide. Our medical device company is headquartered in Lewisville, Texas, and has primary offices in Carlsbad, CA, and Verona, Italy. Our combined company’s global R&D;, commercial and manufacturing footprint also includes facilities and offices in Irvine, CA; Olive Branch, MS; Founded in Verona, Italy, and now headquartered in Lewisville, Texas, Orthofix is proud to be recognized as the 8th Largest Orthopedic Medical Device Company in the World by Medical Design & Outsourcing magazine.

Orthofix is committed to improving patients’ lives and delivering innovative, quality-driven solutions that empower physicians and healthcare organizations to meet the needs of their patients every day. #

📌 Junior International Regulatory Specialist (Verona)
🏢 Orthofix Holdings
📍 Verona