Director of R&D – Software Development

The Director of R&D – Software Development will be responsible for leading our partners research and development programs in advanced 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 the strategic direction while fostering a collaborative, high-performance culture.

The Opportunity Responsibilities

• Strategic Leadership
• Define and execut the 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 image analysis, visualisation, and AI-driven clinical decision support tools.
• Direct, 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 Oversight
• Oversee 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.
• Scout and evaluate emerging technologies (AI/ML models, visualisation 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 Alignment
• Partner 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.

Ideal Profile

• Advanced degree in Computer Science, Software Engineering, Biomedical Engineering, or related field.
• 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, Health Tech, or regulated software (ISO 13485 / IEC 62304).
• Strong understanding of AI/ML, data science, and algorithm development for imaging.
• Excellent communication skills with the ability to align technical, clinical, and business objectives.

Key Attributes

• Visionary 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.