The Globalization Program Manager is a specialized thought leader responsible for driving post-launch global expansion, regulatory registration, and market commercialization portfolios across international markets. Moving beyond standard design-control cycles, this role establishes and executes integrated, cross-functional globalization strategies while ensuring alignment with corporate portfolio priorities, regional demand signals, and budget, scope, and schedule requirements. As a primary bridge between business units, the PM applies expert-level governance to navigate the complexities of international pre-commercialization, regulatory pathways, and global market clearances. They are responsible for evaluating market entry feasibility, filtering dynamic portfolio inputs, and ensuring seamless execution across diverse functional, divisional, and group-level stakeholders. To support collaboration across global time zones, we are seeking candidates located in the Eastern or Central Time Zones. To learn more about Stryker's Neurosurgical portfolio click here: https://www.stryker.com/us/en/nse.html What You Will Do Lead the planning and execution of post-launch global market expansion programs across priority and emerging international markets. Evaluate market entry opportunities using financial models, regional demand forecasts, and supply chain considerations to support portfolio decisions. Develop and execute globalization strategies that align business priorities, regulatory requirements, budgets, timelines, and resource plans. Serve as a subject matter expert on global registrations process, international regulatory pathways, and market clearance requirements, including region-specific regulations. Drive alignment across Research & Development, Regulatory Affairs, Operations, Quality, Engineering, and Marketing teams to support global commercialization objectives . Assess, prioritize, and govern portfolio opportunities using data-driven analysis to support business and market expansion decisions. Identify and mitigate regulatory, operational, commercialization, and portfolio risks to support project execution and prevent downstream business impacts. Prepare and present business cases, technical reports, portfolio analyses, and program updates for executive leadership and governance reviews. What You Will Need Required Qualifications Minimum bachelor's degree in Engineering , Biomedical Sciences, Business Administration, or a related field. Minimum 8 years of experience in project management, program management, or engineering with a highly regulated industry. Experience managing international product commercialization, regulatory registration, or market expansion programs. Experience managing cross-border, multi-site project or program portfolios. Experience supporting global regulatory submissions, registrations, or product clearances. Preferred Qualifications Master's degree in Engineering , Biomedical Sciences, Business Administration, or a related field. Project Management Professional (PMP) certification. Experience in the medical device, healthcare technology, or capital equipment industry.
Posted Date:
07/28/2026 This role will be posted for a minimum of 3 days.
United States of America Pay Ranges:
Puerto Rico :
$102,600
USD Annual USN :
$118,000
- $196,700 USD Annual US5 : $123,900
- $206,500 USD Annual US10 : $129,800
- $216,400 USD Annual US15 : $135,700
- $226,200 USD Annual US20 : $141,600
- $236,000 USD Annual US30 : $153,400
- $255,700 USD Annual View the U.
S. work location and transparency guide to find the pay range for your location.
