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Cadwell

Produces EMG, EEG, IONM equipment

Sustaining Engineering Manager

Engineering LeadershipConfirmed live in the last 24 hours
Full-timeKennewick, WA, USA

About the Job

Requirements

  • Comprehensive knowledge of engineering team leadership, staff development, and the development of engineering procedures, checklists, and work instructions.
  • Comprehensive knowledge of printed circuit board design from concept through manufacturing transfer and post-release support, including Design for Manufacturability and Test analysis.
  • Thorough knowledge of electrical engineering principles, including failure analysis, reliability engineering, component selection, and risk-based decision making.
  • Thorough knowledge of common embedded electronic circuits, including DC-DC converters, embedded microcontrollers, memory interfaces, and sensors.
  • Thorough knowledge of regulatory compliance and quality management systems required for medical devices.
  • Thorough knowledge of the entire hardware development life cycle, including development, testing, change control, deployment to production, and maintenance.
  • Ability to plan, organize, exercise sound judgment, communicate plans and schedules, motivate and lead employees, and collaborate with other teams.
  • Ability to assess, articulate, and manage risk with urgency to meet product requirements, schedule, and budget; see the big picture, prepare contingency plans, and ensure their execution through organizational awareness.
  • Bachelor of Science in Electrical Engineering or equivalent work experience.
  • Typically, more than ten years of relevant professional or technical engineering management experience with increasing responsibility and assignment difficulty.
  • Experience designing regulated equipment; experience in the medical or a similarly safety-conscious, highly regulated industry is ideal.
  • May require reaching, bending, stooping, squatting, crawling, kneeling, pushing, pulling, lifting and carrying up to 50 pounds, finger dexterity, repetitive motions, standing, walking, sitting, hearing, visual acuity, color vision, and two-way written and verbal communication.
  • Extensive computer use is required.
  • Must be able to obtain necessary travel documents.
  • Work hours outside normal business hours may be required at times to meet business needs.

Responsibilities

  • Lead the Engineering Laboratory team in supporting new development and post-release sustaining of the company's medical devices, including failure analysis, design verification testing, component management, production and procurement support, design improvements, and release of new and updated engineering designs.
  • Provide mentorship and guidance to Laboratory Technicians and Engineers, support their technical development, and strategically grow and diversify team skills and composition.
  • Oversee and actively manage Engineering Laboratory resources to ensure effective application across projects and supporting activities; evaluate the team, outputs, and workload to identify and communicate resource needs and schedule impacts, adjusting plans and priorities as needed.
  • Ensure timely resolution of engineering support escalations from other departments and externally sourced escalations from vendors.
  • Lead engineering change control for released designs, chair change control activities, and coordinate cross-functionally with Production, Procurement, and Manufacturing Engineering.
  • Provide direction for Engineering Laboratory standards, processes, checklists, and tools; monitor and manage team and system performance against established goals.
  • Maintain technical expertise to evaluate, guide, and improve team work; ensure work quality meets company design standards and industry best practices.
  • Partner with Procurement, Manufacturing, Service, Software and Hardware Engineering, Regulatory Affairs, Quality Assurance, and Supplier Quality Engineering to provide support as needed.
  • Ensure team processes, training, and outputs align with applicable regulations, including FDA 21 CFR Part 820 and ISO 13485, and company processes; support internal and external audits by the FDA and Notified Bodies.
  • Perform other duties as assigned.

About the Company

Cadwell

Produces EMG, EEG, IONM equipment

Cadwell designs and sells medical neurophysiology equipment, consumables, and software for electrodiagnostic testing, covering EMG, IONM, EEG, and sleep studies. It captures electrical signals with sensors and electrodes, then Cadwell hardware amplifies, records, and CadLink software analyzes the data to support diagnosis and monitoring. The company differentiates itself with a long history of customer feedback, an integrated line of hardware, consumables, and software, and its CadLink data management platform. Its goal is to help clinicians assess nervous system function more reliably so patients receive better care.

Company size
201-500
Company stage
Not listed
Total funding
Not listed
Headquarters
Kennewick, WA
Founded
1979

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