Project Manager

The role

The Project Manager will lead cross-functional projects for products on the market, business systems, and quality programs. They will act as a core team leader to align various departments and drive on-time, high-quality delivery.

What you will do

• Own program timelines, budgets, and deliverables from initiation through release and closure.
• Serve as core team leader to define program scope and secure cross-functional alignment.
• Build and maintain integrated project plans, identifying critical path and resource needs.
• Proactively assess timelines to anticipate risks and develop mitigation plans.
• Lead core team meetings and cross-functional working sessions.
• Lead cross-functional troubleshooting and root-cause efforts for on-market products.
• Develop and implement program metrics, dashboards, and status reporting.
• Escalate issues and tradeoff decisions to leadership.
• Manage suppliers, contract manufacturers, and implementation partners.
• Ensure programs follow design control and change control requirements.

Required qualifications

• Bachelor's degree in related discipline.
• 2-4 years of experience as an engineer or project manager in the medical device industry.
• Track record of delivering product and system changes under formal change control.
• Working knowledge of design controls, change control, risk management, and the medical device product lifecycle.
• Cross-disciplinary understanding of engineering, manufacturing, operations, R&D, IT, clinical, regulatory, and quality functions.
• Experience running several concurrent projects across functions against firm deadlines.
• Strong communication skills to work with coworkers, surgeons, clinicians, distributor representatives, suppliers, and implementation partners.

Nice to have

• Experience in orthopedics; spine or sacropelvic experience is a strong plus.
• Experience in a high-growth medical device company whose products serve a specialty physician audience.
• A history of innovative engineering solutions, cost-effective manufacturing, and ongoing product improvement after launch.
• Experience with ERP or other regulated business-system implementations, including computer system validation.
• Experience managing suppliers or contract manufacturers.
• PMP or equivalent project management certification.
• Proficiency with project management tools (e.g., MS Project, Smartsheet).

About the company

SI-BONE is a fast-growing, publicly traded medical device company that is an industry pioneer in minimally invasive sacropelvic solutions.