Technical Project Manager - Next Generation Ventilator Program

Dormont Manufacturing Co

Franklin (VA)

On-site

USD 80,000 - 100,000

Full time

14 days+

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Benefits offered by this job

Competitive salary and equity opportunity
Health insurance stipend
401(k) plan
Paid PTO and holidays

Job summary

Dormont Manufacturing Co in Franklin, Virginia, is seeking a Technical Project Manager to lead the development of a new Class II ventilator. This role requires a hands-on engineer who excels in cross-team coordination and program execution.

The ideal candidate will have an engineering background and experience in product development, with skills in managing schedules, risks, and vendor interactions. Competitive salary and equity opportunities are available.

Qualifications

  • Up to five years of experience in product development or technical project work.
  • Exposure to electromechanical systems or embedded hardware.
  • Familiarity with ISO 13485, IEC 60601, risk management, or FDA 510(k) processes.

Responsibilities

  • Own day-to-day program execution, including schedule and risk management.
  • Translate product requirements into actionable engineering workstreams.
  • Coordinate closely with various engineering teams to integrate subsystems.
  • Ensure documentation and traceability in accordance with FDA design controls.

Skills

Engineering background (ME, EE, BME, CompE)
Strong technical literacy
Excellent organizational discipline
High ownership mindset

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.


Requirements

What We Are Looking For


  • Engineering background, such as ME, EE, BME, CompE, or related field

  • Strong technical literacy and the ability to interface directly with engineering teams

  • Excellent organizational discipline and a bias for clarity, simplification, and forward progress

  • High ownership mindset and a willingness to run toward problems


Ability to thrive in a fast‑paced, highly collaborative, high‑expectation environment


Preferred Experience

We will take horsepower over years of experience.


Up to five years of experience in product development or technical project work


Exposure to electromechanical systems or embedded hardware


Familiarity with ISO 13485, IEC 60601, risk management, or FDA 510(k) processes


Experience with prototyping, lab testing, or hands‑on engineering work


Benefits

What We Offer


  • A front row seat in a fast‑growing, mission‑driven medtech company

  • Competitive salary and equity opportunity

  • Health insurance stipend, QSEHRA, and 401(k).


Paid PTO and holidays

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