Director of Electrical and Systems Engineer | MedTech

Somerville, Massachusetts Permanent USD200,000 - USD250,000 per year View Job Description
This senior leadership position is responsible for defining, delivering, and sustaining the electrical and systems engineering capabilities that underpin a complex, regulated medical technology platform. The role combines hands-on technical leadership with strategic planning, people management, and cross‑functional collaboration to support both next‑generation product development and existing commercial systems.
  • Leadership Role: End‑to‑End Product Influence
  • Opportunity in the MedTech Space!

About Our Client

The organization operates in the medical technology sector, developing and commercializing advanced systems that directly impact patient outcomes on a global scale.

Job Description

  • Own the end‑to‑end electrical and systems architecture for a flagship, life‑critical medical platform, including design, implementation, testing, and lifecycle support.
  • Lead and influence internal engineering teams and external partners across new product development, sustaining engineering, complaint investigations, and technology obsolescence management.
  • Actively contribute at a technical level by reviewing designs, shaping engineering approaches, and supporting prototype development for both new and existing product lines.
  • Define electrical design inputs, requirements, and specifications aligned with project objectives, regulatory standards, and business needs.
  • Ensure high‑quality design documentation, including design reviews, theory of operation, risk analyses (e.g., DFMEA), and complete release packages ready for manufacturing.
  • Establish and drive verification and validation strategies for electrical subsystems, coordinating internal testing and external laboratory evaluations.
  • Partner with manufacturing and supply chain teams to develop scalable production test methods, fixtures, and process controls.
  • Provide technical oversight and support to contract manufacturers supplying PCB assemblies and electronic components.
  • Investigate and resolve field and quality issues through structured root‑cause analysis and implementation of corrective and preventive actions.
  • Set departmental objectives, track performance, and align resources to meet broader organizational and program goals.
  • Manage project planning, timelines, and budgets while delivering results with minimal oversight.
  • Collaborate closely with Quality, Regulatory, Operations, Supply Chain, and other internal stakeholders.

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.

The Successful Applicant

  • Bachelor's or Master's degree in Electrical Engineering or a closely related discipline.
  • 10+ years of experience designing electrical systems for regulated medical devices.
  • At least 3 years of experience leading and managing engineering teams.
  • Demonstrated experience with Class II or Class III medical devices and compliance with IEC 60601 and related standards.
  • Deep familiarity with medical device regulatory expectations and industry standards.
  • Proven expertise in designing, testing, and formally verifying complex analog and digital electrical systems, including:
    • Microprocessor‑based electromechanical systems
    • Analog front‑end data acquisition
    • Motor control
    • Communications interfaces
    • Power management and lithium‑ion battery systems
    • Physiological monitoring or stimulation technologies
  • Strong project leadership skills, with a track record of driving complex R&D programs from early concept through commercialization.
  • Experience with professional PCB design tools such as Altium and Cadence (OrCAD/Allegro preferred).
  • Excellent written and verbal communication skills with the ability to clearly convey technical concepts to diverse audiences.
  • Ability to operate independently, exercise sound judgment, and deliver results in a fast‑paced, regulated environment.
  • Project management certification or equivalent experience managing large, cross‑disciplinary engineering efforts.
  • Demonstrated success leading teams that deliver high‑reliability electromechanical medical devices compliant with U.S. and international safety and EMC standards.
  • Comprehensive understanding of the full medical device development lifecycle, from early innovation through market release and post‑market support.

What's on Offer

  • Comprehensive benefits package including medical, dental, vision, retirement savings, and paid time off
  • Exposure to cutting edge medical technology and complex engineering challenges
  • Strong emphasis on professional development, mentorship, and long term career progression
  • Hands-on technical role with real ownership and visibility across the organization
  • Stable onsite role with modern lab and office facilities and limited travel requirements



Contact
Marios Peripanos
Quote job ref
JN-042026-6999609

Job summary

Sector
Engineering & Manufacturing
Sub Sector
Engineering Design and R&D
Industry
Industrial / Manufacturing
Location
Somerville
Contract Type
Permanent
Consultant name
Marios Peripanos
Job Reference
JN-042026-6999609