R&D Manager, Programs and Portfolio

Boston Scientific Gruppe; Montreal (administrative region); On-site; CAD 95,000 - 190,000; Full time

Job summary

A global leader in medical technologies is seeking an experienced R&D Manager, Programs & Portfolio in Montreal, QC. The role involves leading Project Managers in developing innovative medical technologies and ensuring compliance with regulatory standards. Candidates should have a bachelor’s degree and over 8 years of relevant experience. This position is critical for aligning product development strategies with patient outcomes. The role offers a competitive salary and requires teamwork in a fast-paced environment.

Qualifications

• 8+ years of experience in product development within a regulated industry.
• Proven experience in project and program management with a track record of launching and sustaining commercialized products.
• Strong understanding of regulatory compliance (FDA, ISO 13485, EU MDR).

Responsibilities

• Manage the team of assigned program managers for the portfolio.
• Lead the development and implementation of coordinated plans to meet company goals.
• Ensure assigned projects are delivered within scope, schedule, budget, and quality levels.

Skills

Project and program management

Product development

Design control processes

Risk management

Communication skills

Problem-solving

Education

Bachelor’s degree in engineering, science, or a related technical discipline

Tools

Project Management certification (PMP, PRINCE2)

Agile development frameworks

Job description

Location: Montreal, QC, Canada.

About the role

The R&D Manager, Programs & Portfolio will lead a team of Project Managers responsible for delivering innovative medical technologies within the Electrophysiology (EP) Capital Equipment business. This role provides leadership and strategic direction across multiple product development programs, ensuring alignment with Boston Scientific’s commitment to improving patient outcomes through meaningful innovation.

Your responsibilities

• Manage the team of assigned program managers for the portfolio as a people manager.
• Lead the development and implementation of a broad, coordinated set of plans and programs to meet the goals and priorities of the company.
• Conduct project baselines and identify project metrics.
• Effectively communicate portfolio and program expectations to team members and stakeholders (including customers) in a timely and clear fashion.
• Continuously improve project management toolkits and methodologies used within PMO.
• Provide expertise and consulting to project managers in the process of project management and in the softer skills of team dynamics, team building and group motivation.
• Ensure assigned projects are delivered within scope, schedule, budget and quality levels are consistent with partner/customer expectations.
• Promote project scope growth and negotiate scope changes with the customers. Manage project closure.
• Standardize project management processes, tools, and metrics to improve efficiency and ensure consistency across projects.
• Implement best practices in time management, cost control, risk management, resource planning, and change management.
• Ensure compliance with FDA Design Control, ISO 13485, and EU MDR requirements within all projects and documentation.
• Develop and maintain strong collaboration with cross‑functional partners across R&D, Quality, Regulatory, Operations, and Marketing.
• Monitor project health and take corrective action when needed to ensure on‑time, on‑budget delivery.
• Encourage continuous improvement by staying informed about industry trends, technologies, and emerging tools in medical device project management.

Required qualifications

• Bachelor’s degree in engineering, science, or a related technical discipline.
• 8+ years of experience in product development within a regulated industry.
• Proven experience in project and program management with a track record of launching and sustaining commercialized products.
• Strong understanding of design control processes, risk management, and regulatory compliance (FDA, QSR, ISO 13485, EU MDR).
• Experience leading cross‑functional and multi‑site teams.
• Excellent organizational, problem‑solving, and communication skills.
• Demonstrated ability to lead through change in a fast‑paced, dynamic environment.
• Willingness to travel up to 25–30%.

Preferred qualifications

• Advanced degree in Engineering, Biomedical Sciences, or Business Administration (MBA).
• Formal Project Management certification (e.g., PMP, PRINCE2, or equivalent).
• Experience with Agile or hybrid development frameworks.
• Strong interpersonal skills with the ability to influence, collaborate, and communicate across all levels of the organization.
• Proven ability to drive operational excellence and process standardization initiatives.

Minimum Salary: $95,600. Maximum Salary: $189,800.

English (oral & written) is required. Knowledge of French is preferred.

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