✦ Luna Orbit — Product Management

Sr. Quality Product Owner - Shockwave Medical

at Johnson & Johnson

📍 Santa Clara, California, United States of America Unknown 💰 $91K – $147K USD / year Posted March 13, 2026
Salary $91K – $147K USD / year
Type Not Specified
Experience mid
Exp. Years Not specified
Education Not specified
Category Product Management

This role involves supporting and optimizing quality application systems within Johnson & Johnson's medical device sector, acting as a liaison between business stakeholders and technical teams.

  • Support quality application systems
  • Liaise between stakeholders and IT teams
  • Develop process documentation
  • Implement system improvements
  • Ensure compliance with standards

The position requires experience with quality management systems, regulatory standards, and system support in a regulated environment, with a focus on process documentation and system enhancements.

The ideal candidate is a mid-level product owner or business analyst with experience supporting quality systems in regulated environments like medical devices. Strong communication and collaboration skills are essential to liaise between stakeholders and technical teams.

Experience supporting quality application systemsAbility to liaise between stakeholders and IT/engineering teams
Experience in medical devicesRegulatory environment knowledge
Quality Management SystemsIT systemsWorkflow documentation tools
Product ManagementBusiness AnalysisQuality SystemsRegulated EnvironmentsSystem SupportTrainingProcess DocumentationSystem EnhancementsIT Support
Product ManagementBusiness AnalysisQuality SystemsRegulated EnvironmentsSystem SupportTrainingProcess DocumentationSystem EnhancementsIT Support
communicationcollaborationproblem-solvingtrainingdetail-oriented
Industry Healthcare & Medical
Job Function Product & Platform Management
Product ManagementBusiness AnalysisQuality SystemsRegulated EnvironmentsSystem SupportTrainingProcess DocumentationSystem EnhancementsIT SupportQuality Application SystemsMedical DevicesRegulatory Standards

Lack of experience in regulated environments, No background in quality systems, Inability to communicate effectively with stakeholders, Unwillingness to work in an unspecified environment

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