Electrical Engineering Manager- Power Tools

Johnson & Johnson Innovative MedicineRaynham, MA
$117,000 - $201,250Hybrid

About The Position

We are seeking top talent for the Electrical Engineering Manager- Power Tools role on our DePuy Synthes Orthopaedics team. This position may be based in Raynham, MA or Palm Beach Gardens, FL. Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of Orthopedics? Ready to join a team that’s reimagining how we heal? Our Orthopedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone Orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes, and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

Requirements

  • BS in Electrical Engineering required; Advance degree preferred
  • 7+ years of electrical engineering experience, with significant exposure to medical devices or other regulated electromechanical systems
  • Prior experience leading or managing engineering teams
  • Prior experience with sterilizable batteries/packs, performance, and cell chemistry
  • Working knowledge of medical device quality systems and regulatory expectations
  • Familiarity with test equipment such as Digital Multimeter (DMM), Oscilloscope, Logic Analyzer, DC Power Supply, and Data Acquisition (DAQ).
  • Schematic layout with CAD tools such as Altium or Cadence
  • Demonstrated ownership of electrical systems from design through development
  • Strong knowledge of electrical controls, circuits, schematics and components
  • Expertise in control systems and circuit design

Nice To Haves

  • Demonstrated experience developing hardware for Class I, II and/or Class III medical devices
  • Familiarity with test equipment such as dynamometer, battery/power analyzer, DC load tester, and BLDC (Brushless DC) motors.

Responsibilities

  • Lead the full lifecycle development of electrical hardware subsystems for Power Tool platforms, from early concept and prototyping through verification, release, and post-market support.
  • Own, define, and evolve the electrical system architecture for Power Tool platforms, including motor controllers, power distribution, and safety circuits.
  • Define component-level and system-level electrical requirements, interfaces, and design standards aligned with clinical use, regulatory requirements, and business objectives.
  • Provide hands-on technical leadership in schematic design, PCB layout reviews, design trade studies, and root-cause analysis of complex system-level issues.
  • Lead the electrical design, integration, and verification of power tools and subsystems, including motor, controller, charger, and batteries.
  • Oversee the development of real-time control hardware, deterministic communication networks (e.g., LINbus, UART), and high-reliability power architectures used in surgical Power Tools.
  • Drive designs that meet requirements for safety, reliability, EMI/EMC compliance, manufacturability, serviceability, scalability, and cost efficiency.
  • Ensure electrical systems comply with applicable medical device standards and regulations, including IEC 60601-1, ISO 13485, and FDA requirements.
  • Support and lead design reviews, risk management activities (FMEA), verification and validation (V&V), and design history file (DHF) documentation.
  • Partner cross-functionally to support architectural decisions, system improvements, and continuous enhancement of overall power platform performance.
  • Lead and participate in architecture reviews, design reviews, and cross-disciplinary technical trade-off discussions.
  • Support design transfer, manufacturing readiness, and product launch activities.
  • Participate in complaint investigations, post-market surveillance, and controlled software updates.
  • Build, mentor, and retain a high-performing electrical engineering team.
  • Identify project critical paths, proactively manage risks, and facilitate cross-functional problem solving.
  • Support resource planning, staffing, and schedule estimation.
  • Communicate risks, opportunities, and execution status clearly to senior leadership.
  • Foster a culture of technical excellence, accountability, ownership, and continuous improvement.
  • Communicate business-related issues, risks, and opportunities to senior management in a timely and effective manner.
  • Interface with regulatory, quality, and manufacturing teams to support audits and inspections.
  • Responsible for communicating business-related issues or opportunities to next management level.
  • Responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable.
  • Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
  • Identify critical paths during product development, address bottlenecks and risks and facilitate problem solving across R&D teams.
  • Support project resource and schedule planning.
  • Performs other duties as assigned.

Benefits

  • Vacation –120 hours per calendar year
  • Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
  • Holiday pay, including Floating Holidays –13 days per calendar year
  • Work, Personal and Family Time - up to 40 hours per calendar year
  • Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
  • Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
  • Caregiver Leave – 80 hours in a 52-week rolling period
  • Volunteer Leave – 32 hours per calendar year
  • Military Spouse Time-Off – 80 hours per calendar year
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