Orthofix Holdings, Inc. in Bussolengo (Verona) is seeking a Technical Product Regulatory Affairs Specialist to join our Regulatory Affairs team as a maternity substitution. You will ensure availability of Technical Documentation File by maintaining EU MDR and FDA submission-ready
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
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 peoples quality of life. At Orthofix, we want
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
Orthofix in Bussolengo (Verona) seeks a Technical Product RA Specialist to join Regulatory Affairs, supporting regulatory documentation for EU/US markets and coordinating with Quality Engineering and R&D. The role is a maternity substitution and reports to Regulatory Affairs
We offer an interesting opportunity to join our Quality Operations team, based in Bussolengo (VR) as Quality Control Engineer , reporting to the Supplier Quality Engineer Supervisor, on a full-time permanent contract. As part of the
Orthofix is seeking a Technical Product Regulatory Affairs Specialist to join the Regulatory Affairs team in Bussolengo (Verona) on a maternity substitution contract. You will ensure availability of Technical Documentation and file updates for EU MDR and FDA submissions.