Sr. Staff Technical Program Manager - Stelo
$156,400–$260,600 year
On-siteSan Diego, California, United States
Job Summary
Lead cross-functional program/project teams driving research, development, and V&V of wearable platforms from feasibility through commercialization. Manage plans and activities across R&D, Commercial, Operations, Quality, Clinical, Regulatory, Finance, and Legal to drive cross-functional alignment of program scope, product roadmaps, and delivery timelines. Resolve internal and external product tradeoffs, manage risks, and make decisions within product contract bounds while communicating strategy and updates to executive leadership. Mentor team members, provide candid feedback for performance reviews, and remove organizational barriers to ensure collaboration. This role supports the Stelo team's mission to reimagine consumer engagement with over-the-counter glucose biosensors through AI-driven insights and partner ecosystem integrations.
Required Qualifications
- Demonstrated successful leadership of a complex medical device development program that introduced new technologies to market, utilizing strong technical, cross-functional, and managed risk leadership
- Demonstrated cross-functional technical leadership and relevant experience across mechanical, electrical, systems, and mobile app engineering disciplines in medical device product development or adjacent industries
- Experience integrating complex hardware, software, and connected mobile experiences
- Driving technical tradeoffs across product architecture, design, verification, validation, and manufacturability
- Partnering with engineering teams to deliver wearable or connected technologies from feasibility through commercialization
- Experience supporting regulatory filings for novel medical technologies or combination medical devices through EU MDR and/or FDA pathways
- Ability to work in environments that are fast-paced and highly dynamic and are comfortable in dealing with a high degree of ambiguity and trade-off
- Excellent communication skills with the ability to convey technical and business information clearly and effectively through documents, reports, and presentations both formally and informal
- Expertise with either stage-gate based product development frameworks and/or software development agile frameworks (medical preferred)
- Experience managing stakeholders inclusive of all technical and leadership levels: working effectively to drive critical program decisions and resolve competing stakeholder interests
- Experience working in the Medical Device industry as well as knowledge of the industry practices, techniques, and standards including a proven ability to both understand and work effectively within a Quality System that is compliant with FDA regulations related to Design Control
- Bachelor's degree in a technical discipline
- Minimum of 13+ years related experience
- Master's degree and 8+ years equivalent industry experience
- PhD and 5+ years of experience
- Must live within commuting distance of your assigned Dexcom site (typically 75 miles/120km)
Desired Qualifications
- Particularly helpful is experience supporting regulatory filings for novel medical technologies or combination medical devices through EU MDR and/or FDA pathways
- Experience with either stage-gate based product development frameworks and/or software development agile frameworks (medical preferred)
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