Globalization Program Manager (Remote)

Stryker Employment Company, LLC; Irvine (CA); Remoto; USD 103.000 - 256.000; Tempo integral

Benefícios oferecidos por esta vaga

Remote work

Resumo da vaga

Stryker is seeking a Globalization Program Manager to drive post-launch global expansion, regulatory registrations, and market clearances across international markets. This remote-friendly role collaborates with R&D, Regulatory, Operations, and Marketing to ensure alignment with budgets, schedules, and portfolio priorities.

Travel up to 20% is required. Ideal candidates hold a Bachelor’s degree in a related field with 8+ years in regulated environments and PM experience; PMP is preferred.

Qualificações

• Bachelor’s degree in Engineering, Biomedical Sciences, Business Administration, or related field.
• 8+ years of experience in project management, program management, or engineering within 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.
• Master’s degree preferred in Engineering,Biomedical Sciences,Business Administration, or related field.
• PMP certification preferred.
• Experience in the medical device or healthcare technology industry.
• Must be legally authorized to work in the U.S. and not require employment-based sponsorship now or in the future.
• US pay ranges include Puerto Rico, USN, US5, US10, US15, US20, US30 with annual USD salaries.

Responsabilidades

• Lead post-launch global market expansion programs across priority and emerging international markets.
• Partner with regional marketing to evaluate market entry opportunities using financial models, demand forecasts, and supply chain considerations.
• Develop and execute globalization strategies aligning priorities, regulatory requirements, budgets, timelines, and resources.
• Serve as SME on global registrations, regulatory pathways, and market clearances including region-specific regulations.
• Drive alignment across R&D, Regulatory Affairs, Operations, Quality, Engineering, and Marketing for global commercialization.
• Assess, prioritize, and govern portfolio opportunities with data-driven analysis for market expansion decisions.
• Identify and mitigate regulatory, operational, commercialization, and portfolio risks to support execution.
• Establish and manage a global governance process for submitting and approving market-expansion requests across regions.

Conhecimentos

Global expansion leadership

Regulatory knowledge

Cross-functional coordination

Market analysis

Project management

Budget & scheduling

Formação

Bachelor's degree in Engineering,Biomedical Sciences,Business Administration or related field

Master’s degree in Engineering,Biomedical Sciences,Business Administration or related field

PMP certification

Descrição da vaga

Work Flexibility: Remote. 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. 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 learn more about Stryker’s Peripheral Vascular portfolio

What You Will Do

Lead the planning and execution of post-launch global market expansion programs across priority and emerging international markets.

Partner with regional marketing to help 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.

Establish and manage a global governance process for submitting, evaluating, prioritizing, and approving market-expansion requests, providing leadership with clear decision criteria and ensuring consistent stakeholder adherence across regions.

What You Will Need

• 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 or healthcare technology industry.
• Must be legally authorized to work in the U.S. and not require employment-based sponsorship now or in the future.
• United States of America Pay Ranges: Puerto Rico: $102,600 - $171,000 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.
• Travel Percentage: 20%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability. Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.

Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes.

We are proud to be named one of the World’s Best Workplaces! For more information, visit: www.stryker.com

Work Flexibility Remote – Role allows you to work the majority to 100% of time from an alternate workplace.

Field-based – You can expect to regularly work a majority to 100% of time at customer facilities and has a set territory or expectation to travel within a set boundary.

Onsite – Role is 100% located at a Stryker facility. Some ad hoc flexibility may be available depending on role, level, and job requirements. Manufacturing roles and any role that requires physical presence at the office would qualify under this category.

Hybrid – You can expect to regularly work in both an alternate workplace and a Stryker facility. Roles that are partially remote or co-located would qualify as hybrid, and the expectation to be onsite would be defined and agreed upon by your manager/supervisor.