Senior Mechanical Engineer - Medical devices

Our Heart Failure R&D team is seeking a Senior Mechanical Engineer to provide technical leadership and hands‑on expertise in the development of Mechanical Circulatory Support devices, specifically Left Ventricular Assist Devices (LVADs).

This role is ideal for an engineer passionate about solving complex problems in life‑sustaining technologies and driving innovation in mechanical and electromechanical systems. You will work cross‑functionally to design, analyze, prototype, and test implantable Class III medical devices
, contributing across the full product lifecycle—from concept through commercialization.

• Specify, design, verify, and validate mechanical components and subsystems for LVADs in accordance with regulatory and quality standards.
• Apply empirical, numerical, and experimental analysis (FEA, CFD, etc.) to evaluate and optimize designs for performance, reliability, and manufacturability.
• Develop and execute test methods and simulation models to mitigate design risks and ensure product robustness.
• Lead design reviews, risk assessments, and technical documentation efforts, including CAD models, specifications, and engineering reports.
• Collaborate cross‑functionally with systems, electrical, software, clinical, and manufacturing engineering teams.
• Interface with suppliers and internal stakeholders to source prototype and production components.
• Mentor junior engineers and foster a culture of technical excellence and continuous improvement.

• Bachelor’s degree in Mechanical Engineering or related STEM field.
• 6+ years of experience in mechanical design and product development, preferably within the medical device industry.
• Proficiency in Solid Works (or equivalent CAD software) and FEA tools (e.g., COMSOL).
• Strong understanding of materials science, manufacturing processes, and design for reliability.
• Demonstrated ability to lead technical projects and deliver results within a regulated environment.
• Excellent written and verbal communication skills, with strong documentation capabilities.

• Experience with Class III implantable medical devices or cardiovascular technologies.
• Familiarity with FDA regulations, EU MDR, ISO 13485, and ISO 14971 design controls and regulatory requirements.
• Exposure to computational modeling, fluid dynamics, and hemocompatibility testing.
• Experience with cable design, electromechanical integration, and biocompatible materials.