PulseMedica is advancing the next generation of ophthalmic medical device technology, and we’re looking for a Project Manager who’s energized by complex, multidisciplinary engineering. You’ll join a team working at the intersection of real-time imaging, AI-driven analysis, precision laser systems, and advanced hardware development - all with the goal of improving vision outcomes for patients.

We are a four-time Great Place to Work Certified company with a highly collaborative, fast-moving engineering culture. By combining cutting-edge research with scalable product development, we’re building breakthrough imaging and laser-based treatment systems that will redefine the future of eye care.

About Us

PulseMedica is redefining the landscape of ophthalmic medical device technology. As a four-time Great Place to Work Certified company, we’ve built a highly cooperative environment where the team accelerates towards breakthrough innovation. Our team develops advanced imaging and laser-based medical device systems that combine classical computer vision, deep learning, and 3D ocular mapping to address diseases that lead to vision loss. By uniting cutting-edge research with scalable engineering, we’re creating treatment solutions that position PulseMedica at the forefront of the next generation in eye care.

The Opportunity

We’re looking for a Project Manager who thrives in complex, multidisciplinary environments and enjoys bringing structure and clarity to technical teams. Reporting to the Senior Project Manager, you’ll guide cross-functional initiatives across software, machine learning, optics, electronics, firmware, mechanical design, and systems engineering.





This role is ideal for someone who wants to contribute to deep-tech innovation, influence how we plan and execute product development, and help deliver next-generation medical devices from concept through commercialization.

The person will be responsible for:

- Developing and maintaining integrated project plans, ensuring projects are delivered on time, within scope, and within budget.
- Owning projects execution across the product development lifecycle, including concept development and feasibility assessment, requirements, design, verification & validation, pre-clinical and clinical activities, and manufacturing transfer.
- Driving project scope definition, objectives, key-results, schedules, and success metrics in collaboration with technical and business stakeholders.
- Managing cross-functional teams across Software, Hardware, Systems Engineering, Quality, Regulatory Affairs, and Operations.
- Owning critical path analysis, dependency management, resource planning, and schedule recovery strategies.
- Leading phase-gate reviews (SRR, PDR, CDR, TRR, Design Reviews, etc.) and ensuring readiness criteria are met.
- Maintaining project documentation and records in accordance with company Quality Management System requirements.
- Identifying, assessing, and mitigating project risks, issues, and dependencies, while driving timely resolution of execution challenges.




- Monitoring project performance using appropriate planning and tracking tools, metrics, and reporting mechanisms.
- Driving Agile, Waterfall, or hybrid development methodologies as appropriate for the project and organizational needs.
- Facilitating alignment between technical teams and leadership while maintaining focus on company objectives and product milestones.

Basic Skills and Qualifications

- Bachelor's degree in Engineering, Science, Health Sciences, Business, or a related technical field.
- 3+ years of project management experience.
- Experience working in highly regulated industries such as medical devices, pharmaceuticals, aerospace, automotive, or defense.
- Experience using project management tools such as Jira, MS Project, Confluence, and Microsoft Office.
- Strong understanding of technical documentation, engineering development processes, and product development workflows.
- Strong analytical, organizational, problem-solving, and communication skills.
- Ability to be physically present in the office at least three days per week.

Highly Desired Skills and Qualifications

- PMP, PRINCE2, Agile, or Scrum certification.
- Experience in medical device development and familiarity with design controls, risk management, verification and validation activities, and manufacturing transfer.
- Working knowledge of ISO 13485, FDA Design Controls (21 CFR 820), IEC 62304, ISO 14971, and related medical device development standards.
- Experience leading projects in startup or high-growth technology environments.
- Ability to understand technical requirements, challenge assumptions, and effectively engage with engineering teams on development

📌 Project Manager, Medical Device R&D (Edmonton)
🏢 Inovait
📍 Edmonton