Staff Project Manager (Medical Devices)

Location: Warwick, RI, United States

Salary: $87,400–$145,625 per year

Company

hirify.global develops and manufactures medical devices and components, including Nitinol components, stents, catheters, delivery systems, biomedical textiles, access kits, guidewires, and precision polymer tubing.

What you will do

• Lead complex, cross-functional customer and internal programs across multiple functions, sites, technologies, and product development phases.
• Own program execution from concept through commercialization, balancing scope, schedule, quality, cost, risk, and financial performance.
• Develop integrated project plans, schedules, milestones, resource requirements, and critical path analyses.
• Identify risks, create mitigation strategies, resolve issues, and facilitate alignment and timely decisions among stakeholders.
• Lead Stage Gate reviews, governance activities, corrective actions, and executive-level project reporting.
• Mentor less experienced Project Managers and strengthen project execution through continuous improvement.

Requirements

• Bachelor’s degree in Engineering, Science, Business, Project Management, or a related technical discipline.
• 5+ years of professional experience, including at least 3 years of project management experience in regulated manufacturing or medical devices.
• Demonstrated success leading large, cross-functional projects with multiple stakeholders and competing priorities.
• Experience managing project budgets, financial performance, scope changes, business cases, and cost models.
• Advanced project planning, scheduling, resource management, risk management, stakeholder influencing, conflict resolution, negotiation, and executive reporting skills.
• Employment visa sponsorship is not available, and candidates on time-limited visa status will not be considered.

Nice to have

• Master’s degree.
• PMP or equivalent project management certification.
• Customer-facing program, multi-site project, or medical device experience.

Culture & Benefits

• Work collaboratively across Engineering, Quality, Operations, Supply Chain, Regulatory, and Commercial functions.
• Operate with substantial independence and judgment while supporting strategic business objectives.
• Partner with customers to move projects from rapid prototyping into high-volume production.
• Work in a regulated medical technology and manufacturing environment.