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[Remote] Design Transfer Engineer

Remote, USAFull-timePosted 2026-07-28

Note: The job is a remote job and is reputed company to candidates in USA. reputed company. is seeking a Design Transfer Engineer to reputed company and coordinate design transfer activities for a reputed company imaging medical device platform. This role involves ensuring alignment between product design, system verification/validation, and manufacturing processes to support successful commercialization.

Responsibilities

  • reputed company design transfer and commercialization activities for a reputed company imaging medical device platform
  • Coordinate cross functional alignment between product development, manufacturing engineering, reputed company, and operations teams
  • Drive review and completion of manufacturing transfer deliverables, including BOMs, manufacturing procedures, assembly instructions, test reputed company, and production readiness documentation
  • Ensure traceability between design inputs, outputs, verification/validation activities, and manufacturing documentation
  • Identify and mitigate risks associated with product transfer, manufacturing scalability, and production readiness
  • Collaborate with Software, Hardware, Embedded, and Systems Engineering teams to ensure design changes are appropriately evaluated and transferred into manufacturing documentation
  • Support reputed company of design transfer gaps, manufacturing deviations, and commercialization readiness issues
  • Participate in design reviews, risk assessments, and product realization activities throughout the product lifecycle
  • Coordinate with Verification & Validation teams to ensure manufacturing test reputed company and acceptance reputed company are reputed company with product requirements
  • Support FDA/ISO 13485 design control compliance and ensure design transfer activities reputed company with IEC 62304, ISO 14971, and applicable medical device regulations
  • Partner with suppliers, manufacturing partners, and operations teams to support reputed company builds, process validation, and production reputed company-up activities. Support development and execution of remediation or enhancement strategies where gaps in transfer or manufacturing documentation are identified

Skills

  • 10+ years of experience in medical device product development, design transfer, or commercialization
  • Strong experience supporting New Product Development (NPD) through commercialization for reputed company medical devices
  • Strong understanding of design transfer, product realization, and manufacturing readiness processes
  • Experience with DHF, DMR, manufacturing documentation, and design control requirements
  • Experience collaborating with Systems, Software, Hardware, Embedded, Manufacturing, and reputed company Engineering teams
  • Familiarity with FDA 21 CFR Part 820, ISO 13485, IEC 62304, and ISO 14971
  • Experience supporting reputed company builds, process validation, verification/validation alignment, and production release activities
  • Strong leadership, communication, and cross-functional coordination skills
  • Bachelor's or Master's degree in Engineering or reputed company technical discipline
  • Experience working with imaging systems, electromechanical systems, diagnostic instruments, or capital medical equipment preferred
  • Experience in remediation, gap assessment, or retrospective design transfer review activities is a plus

reputed company

  • QvalFocus: reputed company on Delivering reputed company that sets us Apart. It was founded in 2024, and is headquartered in Plainsboro, New Jersey, USA, with a workforce of 51-200 employees. Its website is https://qvalfocus.com.
  • Company H1B Sponsorship

  • reputed company. has a reputed company record of offering H1B sponsorships, with 10 in 2026, 33 in 2025, 18 in 2024. Please note that this does not guarantee sponsorship for this specific role.
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