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As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow—because at LivaNova, we don’t just treat conditions — we aspire to alter the course of lives. Location & Travel Houston, TX; Greater New York City, NY area; or Remote Travel: up to 50% regionally The Director, Neuromodulation (NM) Project Head is responsible for managing key projects as it relates to the Obstructive Sleep Apnea (OSA) portfolio. This role provides leadership to cross-functional teams and external partners and manages internal and external stakeholders. The Director, NM Project Head is accountable that the appropriate resources are allocated to ensure that the project meets milestones and deliverables aligned with overall OSA Strategy.
Job Responsibility:
Ownership and accountable to deliver product per the Target Product Profile (TPP) which is aligned to the overall Obstructive Sleep Apnea or Neuromodulation portfolio strategy
Accountable to drive end-to-end project execution
Develops and maintains a detailed project development plan to track progress, manage risks and mitigation to ensure project completion
Identifies potential project risks and work proactively with the core team member and functional leadership and/or external partners to mitigate
Provides guidance and direction to core team as necessary to define clear goals and to evaluate progress
Coordinates with SMEs and necessary approvers to ensure the functional teams deliverables meet the required standards and expectations for project completion
Facilitates change management and communications to ensure a smooth transition to support new product launches
Facilitates team meetings and tracks progress against the project plan while providing executive oversight of the program execution, ensuring timely escalation and resolution of risks and issues
Oversees external partner performance against SLAs and/or SOWs and key milestones
Identifies and assists in clearing barriers to ensure timelines are achieved
Monitors the project budget, ensuring costs are kept within agreed limits and providing regular financial reports to LivaNova OSA & NM leadership
Optimizes the use of resources, ensuring that the external and internal teams are adequately supported and that project resources are utilized efficiently
Resolves project resource issues and facilitates reallocation of activities and efforts to ensure successful project completion
Provides financial insights and recommendations to executive leadership to support strategic decision‑making
Serves as primary connection for internal stakeholders, external partners and other key stakeholders across the OSA and NM organization
Facilitates clear communication to ensure all parties are aligned on project objectives, timelines, and deliverables
Conducts regular meetings with stakeholders to review progress, address concerns, and ensure continuous alignment
Maintains positive and cooperative communication and collaboration with all levels of employees, customers, contractors and vendors
Partners with Security, Privacy, Regulatory Affairs and Quality to ensure business systems and cloud platform adheres to all relevant regulations specific to the medical device industry, such as FDA guidelines, HIPAA, and GDPR
Based on feedback of Security, Privacy, Regulatory Affairs and Quality, prioritizes implementation and execution of work based on regulatory requirements for each product release to ensure on-time submission
Drives operations and process improvement through expertise in process mapping, lean methodology, and the ability to operationalize processes in general
Demonstrates design thinking and facilitate workshops for ideation of process improvement opportunities across the maturity curve
Leads continuous improvement and provide functional areas with the necessary expertise to further improve process maturity after implementation
Coordinates with product design teams in evaluating holistic solutions to internal and external customer needs
Requirements:
BS degree in engineering or science discipline
10+ years of progressively responsible experience leading broad, multi-disciplinary teams, in the medical device industry
Demonstrated experience in leading complex, cross-functional projects and programs
Demonstrated ability to synthesize complex business and technical aspects of small to medium scale development programs
Strong leadership skills, including the ability to set goals and provide positive and constructive feedback respectfully to build positive relationships and improve business results
Strong organizational, planning and follow-up skills and ability to hold others accountable
Ability to work effectively within a team in a fast-paced changing environment
Ability to work in a highly matrixed and geographically diverse business environment
Advanced verbal and written communications with ability to effectively communicate at multiple levels in the organization, including presenting to senior management
Multi-tasks, prioritizes and meets deadlines in a timely manner