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DEKA Research & Development Corp.

Independent R&D lab developing medical devices

Medical Device Software Engineering Lead

Engineering LeadershipConfirmed live in the last 24 hours
Full-timeManchester, NH, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in Computer Science or equivalent work experience, and at least five years of relevant experience.
  • Proven experience as a technical lead or go-to software engineer designing and implementing software/hardware systems for medical devices or other safety-critical, regulated products.
  • Demonstrated experience leading or mentoring junior engineers.
  • Experience developing real-time operating system and embedded systems software, such as FreeRTOS, embedded Linux, or similar safety-critical platforms.
  • Experience with Android application development.
  • Experience defining software requirements and architecture for large, multi-component software systems.
  • Experience developing and verifying software test procedures against defined requirements.
  • Strong troubleshooting skills and ability to adapt rapidly to changing circumstances and technology.
  • Excellent communication skills and attention to detail, with a desire to teach and help others succeed.

Responsibilities

  • Own and drive software architecture, technical direction, and key design decisions across embedded, Android, and cloud layers.
  • Design, implement, and verify medical device software with a focus on reliability, performance, and maintainability.
  • Lead a team of engineers, set planning, standup, and review cadence, and hold the team accountable for progress and quality.
  • Plan releases and maintain status against them, ensuring required features and bug fixes are complete and testing is properly defined and passing before release.
  • Lead technical design, architecture, and code reviews, and mentor junior engineers in technical practice and ways of working.
  • Solve complex system-level problems across hardware and software boundaries in partnership with electrical, mechanical, and biomedical engineering.
  • Define, analyze, and maintain software requirements, interfaces, and development procedures within the FDA design-controls process.
  • Perform software risk and failure mode analysis in accordance with ISO 14971 and ensure lifecycle activities align with IEC 62304.
  • Develop and verify software test procedures to confirm requirements are met.

Desired Qualifications

  • Familiarity with FDA design controls and medical device software standards, including IEC 62304 and ISO 14971.
  • Controls engineering experience.

About the Company

DEKA Research & Development Corp.

Independent R&D lab developing medical devices

DEKA Research & Development Corp. is a leading engineering R&D lab in Manchester, New Hampshire that develops a wide range of practical technologies and devices. It operates by interdisciplinary teams of engineers, machinists, designers, and technicians who take ambitious ideas and turn them into tangible products using advanced design and manufacturing methods. The company differentiates itself through its culture of hands-on experimentation, diverse project portfolio, and a track record of bringing to market or translating ideas into real-world applications. Its goal is to create technologies with a positive, lasting impact on people’s lives by solving meaningful problems.

Company size
501-1,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Manchester, NH
Founded
1982

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