LivaNova

Account Manager

• Achieve or exceed sales objectives and be accountable for daily management of Key Account territory
• Establish and execute long-term strategy for Key Accounts
• Create and maintain business plans for Key Accounts and physician targeting plans for high-potential customers
• Collaborates with and leads TM/TS/MSLs in creation and execution of physician and account strategies using the business plan
• Engage onsite with epileptologists, neurologists, and neurosurgeons/surgeons with latest therapy information, clinical studies, etc. leading to patient identifications
• Identify barriers to VNS Therapy adoption and develop actions and plans to address and overcome the barriers, as appropriate
• Work daily with a high level of integrity and promote a diverse and inclusive workplace culture in both people and thought leadership that is consistent with LivaNova values
• Build and maintain productive professional relationships with customers

Key Account Manager, Epilepsy

QA Engineer

• Leads the supplier selection, evaluation and approval process by assessing manufacturing/ technology capabilities, supplier risk levels, Quality Management System compliance, etc.
• Serves as a core team member on component development teams by providing technical leadership and direction.
• Responsible for supplier process qualification, verification and validation activities
• Reviews supplier process changes for completeness, accuracy, and safety/effectiveness including the identification of all impacts and timely management of these changes with to ensure continued supply of parts
• Acts as business process owner for all supplier related nonconformance report (NCR) management system, including material review board (MRB) activities, monitoring the timeliness and effectiveness of the system and activities;
• Carries out supplier Quality Management System (QMS) and process audits
• Collaborates with suppliers on process manufacturing process improvement, process validation (TMV, IQ, OQ and PQ) and value enhancement opportunities.
• Ensures ongoing compliance per ISO 13485 and MDSAP requirements
• Collaborates with Purchasing and procurement functions to support business strategy initiatives including cost saving efforts, alternate sourcing, outsourced processes etc.
• Provides quality criteria (risk assessment, acceptance criteria, sample size, parameter definition) for receiving inspection activities;
• Ensures that procedures and processes are maintained and updated to be consistent with regulatory changes including the development of more efficient QMS processes and global QMS processes;
• Compiles and presents quality data to management as requested and in management review;
• Contributes to successful regulatory audits by coordinating back room / front room activities or serving as a subject matter expert;
• Supports enterprise resource planning controls and develop systems to ensure that parts and services are provided by approved sources
• Performs other duties as may be required by management.

Senior Supplier Quality Engineer

• Leads the supplier selection, evaluation and approval process by assessing manufacturing/ technology capabilities, supplier risk levels, Quality Management System compliance, etc.
• Serves as a core team member on component development teams by providing technical leadership and direction.
• Responsible for supplier process qualification, verification and validation activities.
• Reviews supplier process changes for completeness, accuracy, and safety/effectiveness including the identification of all impacts and timely management of these changes with to ensure continued supply of parts.
• Acts as business process owner for all supplier related nonconformance report (NCR) management system, including material review board (MRB) activities, monitoring the timeliness and effectiveness of the system and activities.
• Carries out supplier Quality Management System (QMS) and process audits.
• Collaborates with suppliers on process manufacturing process improvement, process validation (TMV, IQ, OQ and PQ) and value enhancement opportunities.
• Ensures ongoing compliance per ISO 13485 and MDSAP requirements.
• Collaborates with Purchasing and procurement functions to support business strategy initiatives including cost saving efforts, alternate sourcing, outsourced processes etc.
• Provides quality criteria (risk assessment, acceptance criteria, sample size, parameter definition) for receiving inspection activities.
• Ensures that procedures and processes are maintained and updated to be consistent with regulatory changes including the development of more efficient QMS processes and global QMS processes.
• Compiles and presents quality data to management as requested and in management review.
• Contributes to successful regulatory audits by coordinating back room / front room activities or serving as a subject matter expert.
• Supports enterprise resource planning controls and develops systems to ensure that parts and services are provided by approved sources.
• Performs other duties as may be required by management.

Supplier Quality Engineer

• Serves as a core team member on software/firmware product development teams by providing technical leadership and direction.
• Responsible for the risk management file, compliance with design control regulations, development of design requirements, architecture specifications, and design verification/validation.
• Chair the change control board within projects for change requests and defects identified during the course of development.
• Lead investigations of software/firmware related complaints, defects identified during development, or from manufacturing nonconformities, audit responses and CAPAs.
• Generates, maintains and updates risk management documentation throughout the life cycle of a product.
• Leads the post-market cybersecurity process by monitoring potential threats and initiating further review and analysis with security experts.
• Ensures compliance with software / firmware development and non-product software validation procedures.
• Contributes to successful regulatory audits by coordinating back room / front room activities or serving as a subject matter expert.

Senior Software Quality Engineer

Compliance

• Support the clinical evaluation activities
• Review promotional materials and support regulatory submissions for active implantable medical devices for the Neuromodulation Business Unit
• Author, prepare and/or update clinical evaluation plans (CEP) and reports (CER) for active implantable medical devices/systems in accordance with EU MDR requirements
• Conduct systematic literature searches, appraisal, analysis, and summarization of data for state-of-the-art, safety and performance periodically
• Manage the overall development and approval process for assigned documents (CEP, CER, etc.) within timelines
• Responsible for regulatory authority queries on clinical evaluation
• Prepare regulatory submissions assigned (510(k); IDE & IDE Supplements; PMA Supplements, notification of change, etc.)
• Direct interface with Regulatory Agencies on assigned projects
• Perform regulatory assessments of changes as part of the change management process
• Promote a diverse and inclusive workplace culture in alignment with LivaNova values

Regulatory and Clinical Specialist

Project Manager

• Define project scope, goals, and deliverables that support business objectives in collaboration with senior management and stakeholders
• Develop detailed project plans, schedules, and budgets, ensuring alignment with the organization's strategic objectives
• Identify and manage project dependencies and critical paths
• Effectively communicate project expectations to team members and stakeholders in a timely and clear fashion
• Coordinate and manage resources for the flawless execution of projects
• Track project milestones and deliverables, providing regular status reports to stakeholders
• Proactively manage changes in project scope, identify potential crises, and devise contingency plans
• Conduct project lessons learned and create recommendations reports to identify successful and unsuccessful project elements
• Foster a collaborative and high-performance environment
• Ensure project documentation is complete, current, and stored appropriately

Customer Support

• Help to make a positive impact on the lives of our patients living with epilepsy
• Collaborate with neurosurgeons, epileptologists, and nurses supporting case coverage for VNS Therapy System
• Responsible for surgical case coverage in the OR during implantation of the VNS Therapy System
• Support Operating Room staff in product-related matters intraoperatively
• Gain or know the local hospitals and be available to work with short notice

Operating Room Support Specialist, Part Time

Marketing

• Develop and lead portfolio‑level marketing strategy and brand management that unites LivaNova’s cardiopulmonary products into a clear, differentiated value proposition for hospital customers.
• Define and maintain integrated portfolio value propositions and core messaging that translate individual product benefits into a compelling system‑level story.
• Partner with product marketing teams to align product‑specific strategies with overarching portfolio narratives, ensuring consistency without sacrificing depth or differentiation.
• Create customer‑facing portfolio tools and content (e.g., value decks, economic narratives, playbooks) tailored to clinical, economic, and executive hospital stakeholders.
• Lead development of economic and outcomes‑based storytelling, including total cost of ownership, utilization efficiency, workflow impact, and long‑term value.
• Support strategic account and IDN engagements by enabling cross‑product discussions and longer‑term planning conversations that extend beyond single purchasing decisions.
• Collaborate with sales, corporate accounts, service, and communication teams as well as outside partners to ensure portfolio value messaging is reflected consistently across commercial strategies, field tools, and customer interactions.
• Identify opportunities to strengthen portfolio differentiation, including bundled messaging, coordinated launches, and integrated product positioning.
• Personally provide marketing management for all Cardiopulmonary service products
• Build and maintain strong relationships with key opinion leaders and emerging thought leaders to influence strategy and stay ahead of market shifts.
• Track and analyze market trends, proactively adjusting strategies and communicating insights to guide organizational focus and market opportunity.
• Track progress of key initiatives, measure impact, and recommend options for improvement.
• Work within LivaNova Ethics and Integrity framework and all industry guidelines to ensure all activities are compliant.
• Take ownership of additional tasks and initiatives as needed.

Portfolio Value Marketing Manager

Recruitment

• Manage full‑cycle recruitment from discovery through offer stage, scaling North America and LATAM hiring efforts during high‑volume recruiting periods.
• Support multiple open requisitions simultaneously while maintaining strong pipeline visibility
• Identify and engage passive candidates through targeted sourcing strategies and direct outreach
• Conduct talent market mapping and competitive talent analysis
• Build proactive talent pipelines for current and future hiring needs
• Partner with hiring managers to understand hiring priorities and role requirements
• Maintain accurate, audit-ready candidate data within Workday or similar ATS platforms in compliance with OFCCP and EEO requirements
• Utilize recruiting metrics and pipeline analytics to track progress and improve hiring outcomes

Senior Recruiter – Talent Acquisition, English, Spanish, Portuguese

Field Engineer

• Performing equipment installations, preventive maintenance, and repairs on customer sites.
• Troubleshooting and resolving technical issues remotely or onsite.
• Providing training and guidance to customers on product operation and best practices.
• Investigate and follow up on service complaints.
• Spare parts management for the field, the role should be responsible for spare parts inventory management following company’s process.
• Be responsible for improving data quality for both the installation base and service reports for the fields.
• Second-line supports for no-Essenz products for distributors service team.
• Promotion and renew service contract.
• Cross-function support and others requested by company as needed.