Principal Electrical Engineer, Medical Devices

in Pharma
  • Madison, WI View on Map
  • Salary: $105,000.00 - $135,000.00
Permanent

Job Detail

  • Experience Level Manager
  • Degree Type Bachelor of Science (BS)
  • Employment Full Time
  • Working Type Hybrid
  • Job Reference 0000007691
  • Salary Type Annually
  • Industry Pharmaceuticals
  • Selling Points

    One of the most senior positions at the site! Requires the ability to teach and mentor others, and a strong capacity for collaboration and helping team members. While there are no direct reports, this position will lead the department.

Job Description

Responsibilities:

  • Lead system-level design analysis and improvements in electrical and electromechanical areas.
  • Collaborate with cross-functional teams to enhance product quality, safety, reliability, and customer satisfaction.
  • Drive product design changes to improve safety, performance, and reduce costs.
  • Support complex root cause investigations, issue resolutions, and other technical projects.
  • Provide expert guidance to manufacturing, reliability, and quality engineering teams.
  • Lead or participate in regulatory compliance activities and safety assessments.
  • Mentor less experienced engineers and support new product development initiatives.

Requirements:

  • Bachelor's degree in Electrical Engineering or related field (Master’s preferred).
  • 10+ years of experience in medical device engineering, preferably in respiratory care or electromechanical devices.
  • Strong problem-solving and analytical skills, with experience in system-level design.
  • Ability to read and interpret technical documentation such as electrical schematics and system specifications.
  • Experience with Failure Modes Effects Analysis, Electromagnetic Compatibility, and relevant regulatory standards.
  • Leadership experience in cross-functional teams and project management.

Preferred Experience:

  • Expertise in medical device technology, especially in respiratory systems.
  • Proficiency with design tools like Altium and knowledge of ISO 13485 and cGMP requirements.
  • Familiarity with accelerated life testing and compliance testing.

Working Conditions:

  • Office, laboratory, and device assembly environments.
  • Some domestic and international travel (up to 20%).
  • ShareAustin:

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