Blue Origin seeks a Technical Program Manager to lead SoC (System-on-Chip) development programs from requirements through production. The role requires managing complex hardware and semiconductor programs across multiple lifecycle phases, coordinating with highly technical engineering teams, external suppliers, and IP providers.… Responsibilities include change management, build-versus-buy decisions, supplier strategy, scheduling, risk management, and translating between detailed technical execution and business objectives. The ideal candidate has 7+ years of technical program management experience, a strong background in IC/SoC development, analog/mixed-signal design, digital ASIC, RF systems, or satellite communications, plus demonstrated ability to lead through tapeout, silicon bring-up, qualification, and production ramp.
six-sigma jobs in San Diego
Staff QA Engineer at Dexcom leading manufacturing quality and regulatory compliance for continuous glucose monitoring devices. Responsibilities include directing Design Control and design transfer strategy, managing process validation and commercialization, leading cross-functional teams on complex technical and compliance matters, and providing expert guidance on Quality Management System governance (FMEA, CAPA, process controls).… Requires deep hands-on experience with FDA 21 CFR 820, ISO 13485, and related QMS requirements, plus ability to mentor teams and represent the organization during audits and regulatory inspections.
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.… 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.