Program Manager, New Product Development (Software)

As a Program Manager within the Program Management Office (PMO), focused on Software New Product Development in Stryker’s Endoscopy Division, you will play a pivotal role in driving the development of innovative medical software products. You’ll collaborate with global teams to deliver cutting-edge software solutions, ensuring that projects are completed on time, within budget, and aligned with business objectives. This is an exciting opportunity to contribute to life-saving technologies in a highly dynamic and innovative environment.

To learn more about Stryker’s Endoscopy portfolio click here: Endoscopy Division

You will need to live within commuting distance to our San Jose, California office for this Hybrid position. You will need to be in the office 3 days a week (including Mondays) and can work from home on other days.

What you will do
• Define and manage program scope in collaboration with business unit leadership.
• Develop detailed project plans, including Agile/Scrum methodologies, Gantt charts, and Work Breakdown Structures.
• Own program schedules, analyzing critical paths and key milestones.
• Create and manage program budgets, optimizing costs within set limits.
• Partner with teams to develop and maintain program quality plans.
• Identify and mitigate project risks with a comprehensive risk management plan.
• Lead procurement strategy and vendor selection.
• Allocate and manage cross-functional resources, defining roles and responsibilities.
• Provide feedback, mentor team members, and support hiring and onboarding.
• Develop stakeholder engagement and communication plans for key business leaders.

What you need

Required Qualifications:
• Bachelor’s of Science Degree in Engineering or related discipline.
• Minimum 8 years of related work experience in Project Management, Software Product Development, or Engineering.

Preferred Qualifications:
• PMP, PgMP, or equivalent preferred.
• Utilization of Agile, rolling-wave, or waterfall planning methodology.
• Lead or developed projects for medical devices or regulated industries
• Experience with project management tools (e.g., Microsoft Project, Smartsheet, or similar).
• Demonstrated ability to make data-driven decisions, balancing risks and benefits in dynamic environments.
• Excellent stakeholder management skills, with the ability to influence without direct authority.
• Strong understanding of quality systems (e.g., ISO 13485, FDA regulations) and risk management practices.
• Proven experience leading cross-functional teams to successfully deliver complex projects on time and within budget.

$150,300 – $245,800 salary plus bonus eligible + benefits. Actual minimum and maximum may vary based on location. Individual pay is based on skills, experience, and other relevant factors.