Senior Director of Software Systems & Digital Platforms (m/f/d), based in Munich
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.
Position Overview
We are seeking a visionary and execution‑focused Senior Director of Software Engineering to lead our software organization across embedded systems and digital health solutions. This role is pivotal in driving innovation, compliance, and delivery excellence in a regulated medical device environment. You will oversee cross‑functional teams spanning Software Engineering, Software Test Engineering, DevOps, and Product Delivery, ensuring alignment with product strategy, quality standards, and market needs.
Key Responsibilities
* Strategic Leadership
o Define and execute the software engineering roadmap across embedded and non‑embedded platforms.
o Partner with Global Strategic Marketing, Quality, Regulatory Affairs, and other stakeholders to align software capabilities with business goals.
* Team Management & Development
o Lead and mentor a multidisciplinary team of engineers, testers, DevOps specialists, and delivery managers.
o Foster a culture of innovation, accountability, and continuous improvement.
* Technical Oversight
o Guide architecture decisions for embedded firmware, cloud‑based platforms, and connectivity solutions.
o Ensure robust design controls and software lifecycle processes compliant with FDA, ISO 13485, IEC 62304, and cybersecurity standards.
* Operational Excellence
o Drive agile development practices, CI/CD pipelines, and scalable DevOps infrastructure.
o Oversee software verification and validation strategies, risk management, and release planning.
* Cross‑Functional Collaboration
o Collaborate with Hardware, Systems Engineering, and Quality teams to ensure seamless integration and compliance.
o Represent software engineering in executive forums and external audits.
* Development Partner Collaboration
o Demonstrated experience working with external development partners, contract manufacturers, or design firms.
o Skilled in managing joint development efforts, ensuring clear communication, milestone tracking, and compliance across organizations.
Skills and Experience
* Bachelor’s degree in computer science, or equivalent.
* Several years of software engineering experience, with some years in leadership roles.
* Proven track record in medical device software development (Class II/III preferred).
* Deep understanding of embedded systems, cloud technologies, and regulated software development.
* Experience with Agile/Scrum, DevOps, and modern software delivery practices.
* Familiarity with HL7, FHIR, and IoT protocols.
* Prior involvement in FDA 510(k), PMA, or EU MDR submissions.
* Strong communication, stakeholder management, and strategic planning skills.
* Experience with AI/ML integration in healthcare applications.
* Ability to travel 25 %.
What We Can Offer You
* A dynamic role in an advanced Medical Device environment interfacing with all worldwide regulatory landscapes supporting your professional career growth.
* Exposure to a State‑of‑the‑Art medical device development process, in close co‑operation with international clinicians.
* Competitive base salary.
* Variable short‑term & long‑term incentives.
* Recognition: through our STARS Program, we recognize and celebrate our colleagues’ contributions and achievements.
Welcome to impact. Welcome to innovation. Welcome to your new life.
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