The Customer Quality Engineer will manage complaint handling, investigations, and regulatory reporting for neuromodulation therapies. They will also collaborate with cross-functional teams to ensure product quality and provide technical support for customer issues.
The Regional Territory Manager supports regional strategy and operational coordination by analyzing market intelligence and managing distributor relationships. The role also involves contributing to business planning and coordinating scientific and marketing programs across the assigned region.
The Global Product Specialist will assist with upstream marketing and product management activities, guiding products from concept through commercial launch. They will collaborate with cross-functional teams to define product features and strategy based on market research and customer insights.
The Territory Manager is responsible for achieving sales objectives and managing the territory by cultivating physician advocates and identifying patient opportunities. They provide clinical education, technical support, and product demonstrations to healthcare providers while managing account relationships and inventory.
The Director will lead a high-performing organization to oversee and advance patient and provider services, ensuring seamless coordination and continuity of care. This role involves driving operational excellence, managing budgets, and collaborating cross-functionally to deliver compliant, patient-focused initiatives.
Drive regional business growth and achieve sales targets through KOL and account management. Coordinate with distributors for order placement and ensure the execution of sales strategies and CRM data accuracy.
Lead the global product labeling strategy and operations for Neuromodulation therapies, ensuring compliance with FDA and EU MDR requirements. Oversee end-to-end labeling activities including UDI management, localization, and the development of IFUs and packaging labels.
Drive commercial strategy and growth within French-speaking Africa by achieving sales targets and managing local operations. Develop distributor networks and maintain relationships with government authorities and key opinion leaders.
The Manager supports market access and reimbursement for medical technologies by engaging with payers, providers, and legislators to ensure comprehensive coverage. Key duties include educating stakeholders on billing and coding and developing tools like budget impact models to advocate for adequate payment rates.
Develop and validate SAS programs to create datasets, tables, listings, and figures (TLFs) for clinical trials and publications. Collaborate with cross-functional teams to ensure programming deliverables meet regulatory requirements and clinical objectives.
Establish and maintain peer-to-peer relationships with healthcare providers and key opinion leaders to provide scientific insights for product development. Execute tactical regional plans and support clinical development initiatives, including investigator-initiated research and product launches.
The role is responsible for driving regional business growth and achieving sales targets through KOL and account management. It also involves managing distributors, executing sales strategies, and maintaining accurate CRM data.
The specialist will author clinical evaluation plans and reports for active implantable medical devices in accordance with EU MDR requirements. They will also review promotional materials for compliance and prepare regulatory submissions for agencies like the FDA.
Establish and maintain peer-to-peer relationships with healthcare providers and key opinion leaders to provide scientific insights for product development. Support clinical development initiatives, medical education, and the communication of clinical data to internal and external stakeholders.
Define and activate the integrated value story for the cardiopulmonary portfolio in North America to shift customer conversations toward holistic partnerships. Lead portfolio-level marketing strategies, create customer-facing value tools, and manage cardiopulmonary service products.
The specialist will design and deploy HL7-based data management solutions and provide second-line technical support for healthcare interfaces. They are also responsible for configuring messaging standards and maintaining comprehensive technical documentation for global teams.
The Clinical Specialist provides clinical and product education to healthcare professionals on the LivaNova Cardiopulmonary portfolio, including in-person and virtual training. They also collaborate with sales and technical teams to support product evaluations, installations, and urgent clinical needs.
The Corporate Counsel will support the company's compliance with U.S. and U.K. securities laws, including SEC filings and Nasdaq listing standards. Additionally, the role involves providing legal support for Board of Directors activities, sustainability disclosures, and global subsidiary management.
This senior leadership role is responsible for building and scaling the first U.S. sales organization for a new Obstructive Sleep Apnea (OSA) product line, requiring the definition and execution of the national sales strategy from the ground up. Key duties include recruiting and leading a high-performing national sales team while driving rapid and sustainable revenue growth for the therapy.
The primary objective is to provide in-house and field-based clinical and technical training and support for medical devices across assigned countries and therapeutic areas, including surgical case coverage and troubleshooting. This involves training healthcare professionals on device usage and surgical procedures, installing, upgrading, and troubleshooting company products, and developing necessary training materials.
