Teams at Orthofix

Administer and maintain internal and external sales commission programs, calculate and validate payouts, manage commission system data, resolve payment discrepancies, prepare reports and support audits while ensuring SOX compliance and collaborating with Sales, Finance, Payroll, and Accounts Payable.

Lead manufacturing engineering for R&D and complex production projects, building engineering teams, managing project plans and budgets, ensuring design control and risk management compliance (FDA QSR/ISO 13485), supervising testing and vendor interactions, mentoring engineers, and driving continuous improvement to commercialize orthobiologic medical products.

Leads design assurance and quality engineering activities throughout medical device development and lifecycle management. Coordinates risk management, usability, design validation, verification, regulatory submissions, technical files, product releases, and post-market surveillance. Partners with R&D, Regulatory Affairs, Clinical Evidence, Marketing, and Quality Compliance to ensure compliance with medical device regulations and standards. Also updates procedures and supports product documentation, with 10–15% travel.