work-breakdown-structure jobs in San Diego

Lead the Sensor Technology workstream for Dexcom's Innovation, Ventures & Sensor Technology PMO, managing biosensing technology development from concept through product lifecycle. Own integrated program timelines, Work Breakdown Structure, and design controls compliance under 21 CFR 820 regulations.…See more Manage budget, resources, risk, documentation in the PLM system, and coordinate build/test activities while serving as the primary stakeholder liaison. This role requires significant medical device development expertise, strong project management skills across waterfall and hybrid methodologies, and preferably a technical background in Material Science or Electrochemistry.

Lead and manage cross-functional teams delivering power distribution and utility engineering projects, overseeing design, construction, budgets, schedules, and resource allocation. Develop project scopes, cost estimates, and Work Breakdown Structures aligned with EPC delivery models while ensuring compliance with utility standards (NERC, IEEE, NEC), environmental regulations, and safety protocols.…See more Manage multiple concurrent projects involving distribution lines, feeders, and grid infrastructure upgrades, performing margin analysis, risk assessments, and earned value management. Coordinate with engineering teams, utilities, municipalities, and regulatory agencies while maintaining project documentation, change control, and closeout activities.

The Systems Engineer applies interdisciplinary expertise to define, develop, integrate, and test complex In Vitro Diagnostic systems for medical device applications. Responsibilities include documenting user and system requirements, decomposing system architecture into subsystems with defined interfaces, conducting hazard and risk analysis, managing configuration and change control, driving system integration and root-cause analysis, and supporting clinical validation.…See more The role requires 10+ years of industry experience with demonstrated mastery of the full product development lifecycle in medical device or regulated environments, including risk management, design reviews, and cross-functional collaboration with development, testing, and clinical teams.