ExecutivePlacements.com
Technical Writer / Editor
ExecutivePlacements.com, Newton, Massachusetts, United States, 02165
Job Overview
We are seeking a Contract Technical Writer to join our Endovascular Robotics business within Advanced Therapies. This role involves translating complex technical engineering processes into clear, accurate, and compliant documentation for a cutting-edge medical robotics system that leverages endovascular robotics, image guidance, and dedicated devices.
Location & Work Arrangement Hybrid: Preferred, but flexible depending on the candidate. Remote work may be up to 90% for highly qualified candidates. Location preference: Initially targeting Boston‑area candidates, open to nearby states (NH, VT, ME) for exceptional profiles.
Compensation $50.00–$65.00 per hour (1st Shift) – Full‑time contract.
Responsibilities
Author and revise IFUs, operator manuals, installation manuals, service manuals, and quick reference guides in accordance with FDA, MDR, and ISO standards.
Translate complex engineering concepts into clear, concise, and accessible documentation for clinical and technical audiences.
Collaborate with cross‑functional teams (engineering, regulatory, human factors, QA) to gather source material and verify/validate content.
Maintain version control and traceability of documentation.
Support risk management and design history file (DHF) documentation as needed.
Assist in developing templates, style guides, and documentation standards.
Qualifications & Experience
Bachelor’s degree in Engineering, Technical Communication, Life Sciences, or related field.
5+ years of experience in technical writing, preferably in medical devices or regulated industries.
Experience writing or leading the creation of user guides for complex electromechanical or software‑based medical devices.
Background in the medical device industry.
Strong attention to detail, organization, and the ability to manage multiple projects.
Excellent written and verbal communication skills.
Familiarity with usability testing, risk management, and regulatory documentation (FDA 21 CFR Part 820, ISO 13485).
Experience with authoring tools (Adobe FrameMaker, MadCap Flare, Microsoft Word) and content management systems.
Experience authoring IFU/operator manuals for highly complex medical devices.
Knowledge of tools such as Adobe FrameMaker, MadCap Flare, and Microsoft Word.
Nice-to-have: Experience with robotic systems and developing training materials.
Ability to work independently and collaborate closely with Systems Engineering, Product Management, and Usability Teams.
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Location & Work Arrangement Hybrid: Preferred, but flexible depending on the candidate. Remote work may be up to 90% for highly qualified candidates. Location preference: Initially targeting Boston‑area candidates, open to nearby states (NH, VT, ME) for exceptional profiles.
Compensation $50.00–$65.00 per hour (1st Shift) – Full‑time contract.
Responsibilities
Author and revise IFUs, operator manuals, installation manuals, service manuals, and quick reference guides in accordance with FDA, MDR, and ISO standards.
Translate complex engineering concepts into clear, concise, and accessible documentation for clinical and technical audiences.
Collaborate with cross‑functional teams (engineering, regulatory, human factors, QA) to gather source material and verify/validate content.
Maintain version control and traceability of documentation.
Support risk management and design history file (DHF) documentation as needed.
Assist in developing templates, style guides, and documentation standards.
Qualifications & Experience
Bachelor’s degree in Engineering, Technical Communication, Life Sciences, or related field.
5+ years of experience in technical writing, preferably in medical devices or regulated industries.
Experience writing or leading the creation of user guides for complex electromechanical or software‑based medical devices.
Background in the medical device industry.
Strong attention to detail, organization, and the ability to manage multiple projects.
Excellent written and verbal communication skills.
Familiarity with usability testing, risk management, and regulatory documentation (FDA 21 CFR Part 820, ISO 13485).
Experience with authoring tools (Adobe FrameMaker, MadCap Flare, Microsoft Word) and content management systems.
Experience authoring IFU/operator manuals for highly complex medical devices.
Knowledge of tools such as Adobe FrameMaker, MadCap Flare, and Microsoft Word.
Nice-to-have: Experience with robotic systems and developing training materials.
Ability to work independently and collaborate closely with Systems Engineering, Product Management, and Usability Teams.
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