Director of R&D

The Director (or Lead) of R&D – Software Development will be responsible for leading Tomoverse Imaging’s research and development programs in advanced cardiac CT imaging software. This role will manage and mentor a growing team of engineers and scientists, ensuring alignment across innovation, regulatory compliance, and product delivery. The Director will set strategic direction while fostering a collaborative and high-performance culture. Key Responsibilities Strategic LeadershipDefine and execute Tomoverse Imaging’s R&D strategy for software development, aligned with corporate vision and regulatory pathways (FDA, Health Canada, EU).Translate clinical, regulatory, and market requirements into technical R&D roadmaps and milestones.Champion innovation in cardiac CT image analysis, visualization, and AI-driven clinical decision support tools.Team Leadership & MentorshipDirect, mentor, and inspire a team of software engineers, data scientists, and imaging specialists.Build team capacity through recruitment, coaching, training, and professional development.Foster an environment of collaboration, accountability, and continuous learning.Guide team members in applying best practices for design, testing, validation, and documentation under ISO 13485, IEC 62304, and other standards.Project & Technical OversightOversee R&D operations, project timelines, budgets, and deliverables.Provide technical leadership on software architecture, algorithm development, and integration of AI/ML pipelines.Collaborate with clinical advisors, KOLs, and internal stakeholders to ensure clinical needs drive development.Ensure robust cybersecurity, privacy, and data governance in line with HIPAA, PIPEDA, and Quebec Law 25.Research, Innovation & PartnershipsScout and evaluate emerging technologies (AI/ML models, visualization methods, cloud/HPC computing).Build collaborations with universities, research hospitals, and technology partners.Oversee preparation of grant applications, publications, and IP filings arising from R&D activities.Regulatory & Quality AlignmentPartner with QA/RA to ensure software development complies with medical device regulations.Support creation of technical documentation, risk analyses, and validation reports for regulatory submissions (e.g., FDA 510(k), Class II).Prepare the R&D team for design reviews, audits, and clinical validation milestones. QualificationsAdvanced degree (MSc/PhD) in Computer Science, Software Engineering, Biomedical Engineering, or related field.10+ years of progressive experience in software development, with at least 5 years in leadership roles.Demonstrated success in leading and mentoring multidisciplinary teams.Proven track record in medical imaging, HealthTech, or regulated software (ISO 13485 / IEC 62304).Strong understanding of AI/ML, data science, and algorithm development for imaging.Excellent communication skills with ability to align technical, clinical, and business objectives. Key AttributesVisionary leader with a pragmatic approach to execution.Strong people manager who develops and empowers talent.Comfortable working in a startup environment with evolving priorities.Passionate about improving patient outcomes through imaging innovation.Skilled problem-solver with ability to balance speed, quality, and compliance.