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. Apply Job!