Software Product Owner

Acumed LLC

Hillsboro, OR, United States
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Digital surgery planning software experience
Voice of customer analysis and prioritization
Cross-functional team leadership and collaboration
** Acumed LLC is seeking a Software Product Owner to define and execute the vision and roadmap for its Digital Surgery Planning software. The role involves acting as a liaison between users, internal teams, and external partners to ensure high-quality software solutions that meet clinical and operational needs. **

Job Summary

  • This role serves as the primary liaison between surgeons, sales, planners, and operations teams to deliver high-quality software solutions.
  • The position requires owning the vision and roadmap for DISRP and Acumed Digital Surgery Planning platforms while translating customer feedback into actionable requirements.
  • Candidates must collaborate with QA and Regulatory Affairs on validation and verification processes to ensure compliance for launches and upgrades.

Matching Summary

Match Score: 75

** Acumed LLC is seeking a Software Product Owner to define and execute the vision and roadmap for its Digital Surgery Planning software. The role involves acting as a liaison between users, internal teams, and external partners to ensure high-quality software solutions that meet clinical and operational needs. **

Skills & Requirements

Must-have

  • Digital Surgery Planning software experience
  • Voice of Customer analysis and prioritization
  • Cross-functional team leadership and collaboration
  • Regulatory Affairs validation and verification knowledge
  • Third-party vendor management capabilities

Nice-to-have

  • Experience with guided surgery or virtual surgical planning
  • Advanced FEA (Finite Element Analysis) proficiency
  • Patent landscape analysis and application support
  • Clinical outcomes data interpretation skills
  • Additive manufacturing for bone fixation knowledge

Key Requirements

  • Bachelor's degree in Mechanical or Biomechanical Engineering preferred
  • 5+ years experience or 10 years medical device development experience
  • Knowledge of 510(k), CE marking, and design-change risk impacts
  • Ability to manage junior staff, vendors, and project schedules independently

Work Rights

Not specified

Tailored Resume

Cover Letter