Career Center

Principal Program Manager, Software

Location: Snoqualmie, WA
Posted On: 04/01/2026
Requirement Code: 73512
Requirement Detail

  • Provide leadership and umbrella guidance to an interdependent family of programs and projects.
  • Work with product management, sales, marketing, and clinical teams to understand the needs of our customers.

  • Manage product requirements, functional specifications, schedules, and risk analyses for programs and projects. 

  • Work with product management and the Change Review Board to prioritize features and technical improvements and build these into the planned product.

  • Program Planning - Collaborates with stakeholders (engineering and test teams, product managers, and senior leadership, etc.) to define the scope, objectives, and deliverables of the projects/program. Develop detailed project plans (MS Project and Microsoft Azure DevOps), taking into account resource availability, timelines, and budget constraints.

  • Manage and continually improve the process for planning, execution, and refinements for Program Increments, Sprints, and the overall project schedule.

  • Work in tandem with software project managers to define, measure, analyze, improve, and Control (DMAIC) all aspects of software delivery, including performance metrics of team members, teams, and overall project/program performance.

  • Ensure delivery of the market deliverable targets of the family of programs.

  • Mentor and guide fellow program and project managers within the PMO.

  • Manage the development of required plans and documentation for all development activities.

  • Lead cross-functional teams to deliver on the plan, with a constant focus on delivering high-quality products that meet customer expectations; follow the Spacelabs QMS; and are fully compliant with government regulations across our customer base, including FDA, CSA, EU, CFDA, and others.

  • Build, drive, and support cross-functional teams through the development process. Set expectations and lead project delivery skill-building among team members.

  • Continuously seek innovative ways to improve development productivity through the introduction of new technologies, systems, methods, and controls.

  • Provide communications and formal project reviews with senior management, the program team, and others as required. 

  • Eliminate barriers, escalate issues as appropriate, and provide visibility into development status for other stakeholders. Provide frequent communications and formal project reviews with senior management, program team, and others as required.

  • Negotiate schedule, risk, product features, and resource trade-offs with project and program teams.

  • Uphold the Company’s core values of Integrity, Innovation, Accountability, and Teamwork.

  • Demonstrate behavior consistent with the Company’s Code of Ethics and Conduct.

  • Ensure that direct report(s) are trained and evaluated on their knowledge and adherence to the company’s values, Code of Ethics and Conduct, and applicable compliance policies.

  • It is the responsibility of every Spacelabs Healthcare employee to report to their manager or a member of senior management any quality problems or defects in order for corrective action to be implemented and to avoid the recurrence of the problem.

  • Duties may be modified or assigned at any time to meet the needs of the business.

  • Bachelor of Science degree in Engineering, Computer Science, or a similar related degree. A master’s degree is desirable.

  • 15+ years’ experience in software development.

  • 5+ years' experience in medical device development compliant with IEC 62304.

  • 5+ years’ experience in program management.

  • 5+ years’ experience in managing complex interdependent new product development projects within demanding timeframes required. Solid understanding of the development process, including requirements gathering, analysis and design, development tools and technologies, release and version control, contemporary testing methodologies, and deployment management.

  • 5+ years’ experience with Agile / Lean Software Development Lifecycle processes.

  • Knowledge of FDA and medical device regulatory and registration requirements or work in a similarly regulated industry is desirable.

  • Demonstrated track record of encouraging innovation and out-of-the-box thinking.
  • Proven ability to deliver results through others, both in direct and matrixed organizational models. 

  • Proven ability to lead dedicated, passionate teams, including an ability to motivate and hold others accountable, including international teams.

  • Excellent communication and negotiation skills, for both internal and external audiences, at all levels.

  • Experience in specifying and shipping software for use in cloud environments is highly desirable. 

  • Knowledge of and ability to work within a global corporate environment is required.
  • Must travel internationally and be able to acquire all necessary travel documents. 

  • Travel up to 15%.

  • PMI, PMP, or PMI-ACP Certification preferred.