Director, Device Engineering

Beacon Biosignals

Boston, MA, United States
Base: $200,000–$215,000; equity: included in total...
On-site
10+ years post-graduate hardware engineering experience
Fda and ce regulated product commercialization
5+ years direct people management experience
Beacon Biosignals is revolutionizing precision medicine for the brain with its at-home EEG platform supporting clinical development of novel therapeutics

Job Summary

  • Beacon Biosignals is revolutionizing precision medicine for the brain with its at-home EEG platform supporting clinical development of novel therapeutics.
  • The Director of Device Engineering will own the end-to-end lifecycle of home sleep testing products from concept through mass production and sustaining engineering.
  • This role requires leading a multidisciplinary team to deliver safe, reliable medical devices that meet rigorous FDA and ISO regulatory standards.

Matching Summary

Beacon Biosignals is revolutionizing precision medicine for the brain with its at-home EEG platform supporting clinical development of novel therapeutics.

Salary

Base: $200,000–$215,000; Equity: Included in total compensation package; Benefits: PTO and other benefits included

Skills & Requirements

Must-have

  • 10+ years post-graduate hardware engineering experience
  • FDA and CE regulated product commercialization
  • 5+ years direct people management experience
  • Wearable devices and embedded systems expertise
  • FDA 21 CFR Part 820 and ISO 13485 knowledge
  • EVT DVT PVT build and manufacturing transfer
  • Design control execution and risk management

Nice-to-have

  • Startup or high-growth company experience
  • MS or PhD in Engineering preferred
  • Cloud-native analytics platform familiarity
  • AI algorithms integration experience
  • Cross-functional leadership in dynamic environments

Key Requirements

  • Bachelor's degree in Engineering required; MS/PhD preferred
  • 10+ years post-graduate experience in hardware/device engineering
  • 5+ years of direct people management experience
  • Experience with FDA 21 CFR Part 820 and ISO 14971
  • Hands-on experience with EVT/DVT/PVT builds

Work Rights

Not specified

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