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Posted 7mo ago

Technical Project Manager - Next Generation Ventilator Program

@ Enexor
Franklin, Tennessee, United States
OnsiteFull Time
Responsibilities:Own program execution, Translate requirements, Coordinate subsystems
Requirements Summary:Engineering background; strong technical literacy; ownership mindset; ability to interface with engineering teams; thrive in fast-paced, collaborative environment.
Technical Tools Mentioned:ISO 13485, IEC 60601, FDA 510(k), Regulatory compliance, Prototyping tools
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Job Description

About Us

We are an early-stage company developing disruptive medical technologies that challenge industry norms and dramatically reduce cost and complexity. Our small, hands-on team designs, builds, and validates next-generation medical devices entirely in-house from concept through FDA submission.

If you are motivated by complex problems, rapid iteration, and creating products that make a real impact, this is the place where your work will matter every day.

The Opportunity

We are recruiting a Technical Project Manager to drive the end-to-end development of a new Class II ventilator. You will be the connective tissue across mechanical, electrical, firmware, industrial design, manufacturing, and regulatory teams, keeping the program aligned, moving forward, and delivering results.

We are not looking for a career PM who hides behind process. We want a sharp, driven engineer who thrives on ownership, clarity, and execution. If you can think like an engineer but operate like a program leader, you will excel in this role.

What You Will Do

  • Own day-to-day program execution, including schedule, risk management, deliverables, and cross-team coordination

  • Translate product requirements into actionable engineering workstreams and hold teams accountable.

  • Design reviews, maintain the engineering backlog, and drive decision-making with incomplete information.

  • Coordinate closely with mechanical, electrical, firmware, and industrial design teams to integrate subsystems.

  • Manage vendor interactions, including ID and UX firms, PCB vendors, plastics suppliers, sensor suppliers, test labs, and manufacturing partners.

  • Ensure documentation, DMR, and DHF organization, traceability, and test readiness in accordance with FDA design controls.

  • Support prototyping, V and V planning, test execution, and system integration when needed. This role is hands-on.