Search the 28 jobs at Orthofix

The Set Sourcing Specialist will provide logistical support managing inventory requests for surgical instruments and implants. Responsibilities include order fulfillment, communication with distributors, tracking inventory, processing transactions, and ensuring timely delivery. The role requires strong communication skills and attention to detail while maintaining relationships with internal and external partners.

The Software Developer I supports the design, development, testing, documentation, and maintenance of software for the FLASH navigation system while ensuring compliance with applicable regulations.

The Insurance Administrator I role involves verifying patient insurance benefits, performing insurance-related tasks, and ensuring timely order processing while maintaining effective communication with internal and external stakeholders. The position requires attention to detail, strong organizational skills, and the ability to manage multiple priorities while adhering to compliance standards.

The Bone Growth Therapies Specialist provides field training on the use and promotion of Orthofix’s Bone Growth Therapy devices. Responsibilities include training sales representatives, assisting in territory analysis, and supporting sales efforts by liaising with various departments and stakeholders.

The Senior Product Manager - Biologics will be responsible for managing marketing strategies for specific bone grafting products. Key duties include developing strategic business plans, launching new products, managing sales support activities, and collaborating with various teams to achieve business targets and improve processes.

The Product Manager will oversee the marketing of spinal implant products, focusing on strategic business planning, managing product development activities, collaborating with departments for product launches, and providing support to the sales team. Responsibilities include market analysis, product positioning, and identifying process improvements.

The Product Manager is responsible for overseeing the marketing of Enabling Technologies products, creating business plans, managing product development marketing activities, launching new products, and collaborating with various departments to ensure effective product management and sales support. It requires analysis of market trends and ongoing product lifecycle management.

The Document Control Specialist coordinates document control activities, manages documentation accuracy, maintains compliance with quality management systems, and supports internal and external audits. This role includes organizing the approval process for controlled documents, collaborating with subject matter experts, and providing support for compliance with regulatory standards.

As a Software Developer II, you will design, develop, and test software for the FLASH navigation system, participate in the software development life cycle, document requirements, review code, and collaborate with quality assurance and clinical specialists, while also mentoring junior team members.

The Software Developer III will design, develop, test, document, and maintain software for the FLASH navigation system, while participating in the software development lifecycle, code reviews, and collaborating with QA and clinical specialists. Responsibilities include clarifying requirements, ensuring code quality, and mentoring team members.

The Group Product Manager is tasked with managing a group of products, developing and executing marketing plans, leading a product marketing team, and achieving revenue targets through innovative strategies and market analysis.

The Executive Assistant provides day-to-day administrative support to Executive Leadership Team members, enhancing their effectiveness through time management, scheduling, correspondence handling, and travel planning. The role includes mentoring other team members, preparing reports and presentations, managing expenses, and organizing events to support the executives' needs.

As a Senior Quality Engineer, you'll lead and coordinate quality objectives in product development, ensuring compliance with quality systems and regulatory standards. You will conduct risk management, develop inspection plans, support calibration activities, and facilitate product launches while aiming for continuous improvement within the quality framework.

As a Territory Manager at Orthofix, you will promote and distribute bone growth therapy devices while providing outstanding customer service. Your key responsibilities include directly engaging with physicians and patients, educating on product use, maintaining relationships with healthcare providers, and achieving sales targets. Additionally, you will prepare sales orders and resolve customer issues promptly.

The Quality Engineer is responsible for overseeing Quality Engineering activities related to product support and transfer, approving documentation, leading cross-functional teams, and ensuring compliance with regulatory standards. They also develop inspection plans, manage risk assessments, support quality control, and drive continuous improvement.

The Supplier Quality Engineer will lead supplier evaluation, performance assessment, and corrective action processes. Responsibilities include conducting supplier audits, maintaining quality metrics, and improving supplier management procedures. Travel is necessary to perform supplier audits and support external audits.

The Document Control Specialist at Orthofix will manage document control activities, ensuring compliance with FDA and ISO standards. Responsibilities include coordinating the document approval process, maintaining the Quality Management System, and supporting audits. This role requires collaboration with various departments to enhance documentation processes and provide support for technical projects.

The Senior Quality Engineer, Design Assurance is responsible for quality engineering activities related to product development and existing product support, leading cross-functional teams, reviewing and approving quality documentation, facilitating product launches, and supporting risk management and quality control efforts.

The Associate Product Manager – Biologics will manage marketing activities for bone grafting solutions, executing strategies and plans, supporting product launches, and collaborating with multiple departments to ensure alignment and achieve objectives.

The Senior Quality Engineer is responsible for quality engineering activities in product development, approving quality documentation, leading cross-functional projects, managing risk assessments, developing inspection plans, and supporting regulatory compliance for new product launches and technology transfers.