Orthofix
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The Territory Operations Manager supports Territory Managers and Associate Territory Managers by managing documentation, inventory control, and communication with patients and medical staff. This role involves ensuring order completion according to insurance guidelines and tracking patient interactions, along with onboarding staff and managing reporting processes.
The Supplier Quality Engineer will support supplier management operations, conduct audits, resolve quality issues, track supplier metrics, and ensure continuous improvement in quality management processes. Responsibilities include maintaining the Approved Supplier List and assisting during external audits.
The Senior Product Manager is responsible for managing marketing for specific product franchises, establishing long-term strategies, executing marketing plans, and launching new products. The role involves collaborating with various departments, analyzing data, and providing support to sales teams.
The Senior Quality Engineer is responsible for quality engineering activities related to product development and support. This includes approving quality documentation, leading cross-functional teams, facilitating risk management activities, and ensuring compliance with regulatory standards while supporting new product launches and maintaining quality control processes.
The Associate Quality Engineer will engage with teams and suppliers to drive quality performance, support complaint investigations, initiate corrective actions, track quality metrics, and ensure compliance with standards. They will also contribute to continuous improvement initiatives and develop inspection procedures and work instructions.
The Set Sourcing Specialist I provides logistical support to sales representatives by managing inventory for surgical instrument requests, ensuring order fulfillment, and resolving delivery issues. Responsibilities include tracking inventory, communicating with distributors, and maintaining documentation while meeting quality and service standards.
The Product Manager for Enabling Technologies will establish product strategies, manage marketing activities, and ensure successful product launches while collaborating with multiple departments to achieve business performance targets.
The Document Control Specialist manages document control activities related to document and data management systems, ensuring compliance with quality systems and regulations. Responsibilities include tracking and auditing controlled documents, maintaining the Quality Management System, collaborating on controlled documents, and supporting regulatory compliance activities.
The Software Developer II designs, develops, tests, and maintains software for the FLASH navigation system, collaborating across teams and participating in the software development life cycle while mentoring junior members.
The Software Developer III is responsible for designing, developing, testing, and maintaining software for the FLASH navigation system. Duties include participating in the entire software development life cycle, clarifying requirements, writing documentation, conducting code reviews, mentoring team members, and collaborating with QA and clinical specialists while ensuring compliance with regulations.
The Group Product Manager is responsible for overseeing a specified portfolio of products, developing global strategies and marketing plans, and ensuring successful product commercialization. This role also involves leading a product marketing team, conducting market analysis, and coordinating product launches to meet revenue targets.
The Executive Assistant will manage administrative functions, coordinate travel, handle confidential information, organize executive files, prepare expense reports, and support the executive team, ensuring efficient operation of the office.
The Senior Quality Engineer is responsible for overseeing Quality Engineering activities for product development, approving Quality System documentation, leading cross-functional teams on quality objectives, and interfacing with different departments to ensure compliance and facilitate new product launches within the medical device sector.
Supervise the Insurance Administration team while ensuring compliance, organizational standards, and training new sales representatives. Responsibilities include monitoring order processing, maintaining business metrics, and fostering a positive work environment.
The Supplier Quality Engineer will manage Supplier Quality operations, including audits, corrective actions, and quality metrics. They will work with cross-functional teams to enhance supplier performance and engage in continuous improvement programs, ensuring compliance and optimal processes in supplier management.
The Senior Quality Engineer in Design Assurance leads quality engineering activities, reviews and approves quality documentation, develops design history files, manages risk assessment processes, and ensures compliance with medical device regulations. They facilitate new product launches, support quality control and calibration, and conduct investigations to resolve quality issues.
The Territory Manager promotes and distributes Orthofix's bone growth therapy devices, working closely with physicians, patients, and distributors to meet sales quotas. Responsibilities include providing customer service, training, and developing new accounts, as well as attending meetings and conventions.
The Territory Manager for Bone Growth Therapies promotes and distributes Orthofix products, achieving sales quotas, providing consultative service and education to physicians and patients, and developing new accounts while maintaining existing relationships. This role also requires problem-solving with clients and preparing necessary documentation for sales orders.
The Associate Product Manager - Biologics is responsible for managing marketing strategies for bone grafting solutions, executing product launches, and achieving sales targets. Duties include developing sales materials, market analysis, collaborating with cross-functional teams, and supporting product development initiatives.
As Associate Manager in Product Development, you'll oversee projects involving spinal implants and instruments from concept to market, manage engineering teams, coordinate design and manufacturing processes, ensure regulatory compliance, and enhance efficiency through cross-functional collaboration.