Program Manager

Mason Alexander; Burlington; On-site; CAD 100,000 - 120,000; Full time

Job summary

A leading medical device company in Burlington, Canada, is seeking an experienced Program Manager to lead the development of a groundbreaking cardiac support device. The role requires a Master's degree and over 10 years of experience in medical device development. You will champion a culture of quality while collaborating with diverse teams to align product development with market needs. This is a unique opportunity to make a real impact in patient care.

Qualifications

• 10+ years of experience in medical device development, preferably with cardiovascular devices.
• Deep knowledge of interventional cardiology and regulated development environments.
• Experience in start-up or entrepreneurial settings is a strong plus.

Responsibilities

• Lead the execution of cardiac support device program from development to manufacturing.
• Develop and implement program plans, risk assessments, and design reviews.
• Collaborate with marketing, regulatory, and clinical teams.
• Manage program budgets, timelines, resources, and communications.
• Champion a culture of quality and continuous improvement.

Skills

Leadership

Communication

Organisational skills

Knowledge of interventional cardiology

Education

Master’s degree in biomedical or related engineering discipline

Job description

Are you ready to lead innovation in cardiac care? A forward-thinking medical device company is seeking an experienced Program Manager to drive the development of a groundbreaking heart support device used in interventional cardiology.

This is a unique opportunity to make a real difference in patients' lives while shaping the future of cardiovascular therapy. Join a dynamic, diverse, and ambitious team operating at the forefront of MedTech innovation.

Responsibilities:

• Lead the execution of a novel cardiac support device program from development through manufacturing scale-up.
• Develop and implement program plans, risk assessments, and rigorous design reviews.
• Collaborate with marketing, regulatory, and clinical teams to align product development with market and clinical needs.
• Manage program budgets, timelines, resources, and communications across stakeholders.
• Champion a culture of quality, compliance, and continuous improvement.

Qualifications:

• Master’s degree in biomedical or a related engineering discipline (or equivalent experience).
• 10+ years of experience in medical device development – cardiovascular devices preferred.
• Deep knowledge of interventional cardiology and regulated development environments.
• Exceptional leadership, communication, and organisational skills.
• Experience working in start-up or entrepreneurial settings is a strong plus.

Be part of an exciting growth journey with a team committed to making a real impact in patient care. You'll enjoy autonomy, collaboration, and the chance to work on something truly meaningful.

Apply now or reach out directly to learn more.