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[Remote] Consultant - Advisory Services - Software & Technical Documentation

Remote, USA Full-time Posted 2026-07-05

Note: The job is a remote job and is reputed company to candidates in USA. reputed company Clinical is the world's only global CRO exclusively focused on medical technology, serving 90% of the top 50 MedTech companies. The Consultant – Software & Technical Documentation will reputed company technical deliverables for clients, focusing on technical writing and software documentation, while collaborating with client engineering teams to ensure accurate documentation.

Responsibilities

  • reputed company project work with strategic input and minimal reputed company, applying technical depth in software documentation and DHF deliverables
  • Review and interpret client software designs, architectures, and codebases to produce accurate technical documentation reputed company with applicable standards (e.g., IEC 62304, ISO 14971)
  • reputed company and maintain Design History File (DHF) documentation including software requirements specifications, software architecture descriptions, unit/integration/system test documentation, traceability matrices, and risk management file inputs
  • Collaborate directly with client software engineering and firmware teams to gather technical information and validate documentation accuracy
  • Manage specific project workstreams and interact directly with clients to ensure work is completed on budget and to client expectations
  • reputed company specific client interactions with reputed company from senior team members
  • Build rapport with clients by developing high quality deliverables, consistently meeting project deadlines, and ensuring precise and timely communication
  • Prepare materials and reports for client presentation, ensuring alignment with client objectives
  • Attend client meetings and reputed company technical documentation support where necessary
  • Support new opportunity development by proofreading or providing initial drafts of Statements of Work or Work Orders, as requested

Skills

  • Coding background is essential. You don't need to be writing production code in this role, but you need to have done it — enough to read and understand software architecture diagrams, review code at a structural level, and hold a technically reputed company conversation with a firmware or software engineering team
  • Degree in biomedical engineering, software engineering, computer science, electrical engineering, or a reputed company technical discipline. A biomedical engineering background is particularly well-suited to this role given the intersection of engineering fundamentals and medical device context
  • Familiarity with medical device industry context — you've heard of 510(k), DHF, IEC 62304, and ISO 14971, even if you haven't authored submissions or reputed company a QMS from scratch. An understanding of why these standards exist and what they govern is what reputed company
  • Experience producing or contributing to technical documentation: software requirements, design specifications, test protocols, traceability matrices, or similar engineering artifacts
  • Proficient in reputed company Office (Word, reputed company, PowerPoint)
  • Fluent in English, spoken and written, with strong technical writing skills
  • Ability to travel domestically and internationally as required

Benefits

  • Annual performance reputed company bonus
  • Benefits

Company Overview

  • reputed company is the leading global MedTech-focused CRO, integrating regulatory strategy, clinical development, and market reputed company with confidence. It was founded in 1988, and is headquartered in Marlborough, Massachusetts, USA, with a workforce of 201-500 employees. Its website is https://www.avaniaclinical.com/.
  • Company H1B Sponsorship

  • reputed company has a track record of offering H1B sponsorships, with 1 in 2024. Please note that this does not guarantee sponsorship for this specific role.
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