Jobs at LivaNova

Lead US market access and reimbursement efforts for medtech products by engaging payers, providers, hospitals, and policymakers; develop evidence summaries, budget impact models, reimbursement guides and advocacy tools; train internal and external stakeholders on coding and reimbursement; monitor and influence healthcare policy; collaborate with commercial teams to secure comprehensive coverage and adequate payment.

Develop, validate, and maintain SAS programs to produce SDTM/ADaM datasets and TLFs for clinical trials. Collaborate with Statistics, Data Management, clinical teams and vendors, ensure quality, traceability, and regulatory compliance (CDISC), support SAP/analysis specs, and contribute to process modernization and standardization.

Hybrid HR & Office Coordinator for Benelux responsible for Belgian payroll administration, employee lifecycle (onboarding/offboarding/benefits), compliance with local labor regulations, HQ audit support, daily office operations, vendor/contract management, budget and invoice oversight, health & safety initiatives, and employee engagement events.

Part-time Workplace Coordinator responsible for day-to-day office operations in Gloucester: managing facilities and vendors, office supplies, mail, basic finance tasks, compliance support (ISO, fire safety, first aid), meeting logistics, and providing administrative support and onboarding assistance.

The Software Test Engineer verifies software functionality, performance, and safety for medical devices, ensuring compliance with regulations and quality standards.

The Marketing Operations Specialist supports marketing execution in APAC & Growth Markets, managing compliance, event logistics, and cross-functional collaboration to ensure efficient operations and adherence to standards.

Lead strategic workforce planning, skills-based approaches, internal mobility, and AI-enabled work redesign. Build tools, analytics, and processes to translate strategy into capabilities, roles, and workforce mix, advise leaders, drive adoption across HR, Finance, IT, and business partners, and increase internal mobility and productivity.

The role involves conducting failure investigations and quality assessments for electro-medical devices, collaborating across functions, and developing test methodologies.

Provide field-based OR support during implantation of the VNS Therapy System, assist OR staff with intraoperative device diagnostics, troubleshooting, and programming, maintain credentialing and immunizations, travel to hospitals within territory, and be available on short notice for part-time case coverage (up to 29 hours/week).

Provide intraoperative product support for VNS Therapy implantations in operating rooms. Support OR staff with diagnostics, troubleshooting, and programming assistance, maintain hospital credentialing and immunizations, travel to hospitals within territory, and work part-time on short notice up to 29 hours weekly.

The Office Manager will oversee daily administrative operations, manage office resources, support staff, and ensure a positive work environment.

Perform quality engineering for Class II/III medical devices, investigate nonconformances and complaints, lead CAPA and risk assessments, support suppliers and validations, maintain quality records, and drive process improvements to meet regulatory and customer reporting requirements.

Conduct internal audits per the annual plan, evaluate internal controls and regulatory compliance, support audit documentation and submissions, coordinate internal/external audits and remediation, and assist with audit-related data analytics and risk assessments across global medtech operations.

Serve as technical liaison between internal teams and suppliers to manage supplier selection, audits, process qualification/validation, NCR/CAPA, and supplier process improvements. Ensure compliance with ISO 13485/MDSAP, support receiving inspection criteria, present quality data, and collaborate on cost-saving and sourcing initiatives. Travel up to 25% and support regulatory audits and QMS process updates.

The Senior Software Design Assurance Quality Engineer leads product development, ensures compliance with regulations, and oversees software quality processes while collaborating with various teams to enhance product safety and effectiveness.

The Portfolio Value Marketing Manager leads the marketing strategy for LivaNova's cardiopulmonary portfolio, focusing on integrated value propositions, customer engagement, and collaboration across teams to enhance hospital partnerships and drive value-based solutions.

The Technical Services Specialist role involves leveraging HL7 expertise, providing 2nd-line support, configuring healthcare messaging standards, and developing solutions in a healthcare IT environment.

The Senior Supplier Quality Engineer leads supplier evaluation, ensures compliance with quality standards, and collaborates on manufacturing improvements, focusing on regulatory requirements and cost-effective solutions.

The Supplier Quality Engineer ensures supplier compliance and quality assurance by developing processes, conducting audits, and managing corrective actions to meet customer requirements and minimize quality costs.

Support the P2P process within the organization, providing assistance with SAP transactions, resolving vendor queries, and monitoring service health while ensuring compliance with P2P policies.