Technical Writer (Medical Devices)

Technical Writer (Medical Devices)

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TECHNICAL WRITER (Medical Devices) We are looking for a

proactive, precise, and strong communicator

to join our team as a

Technical Writer

in the medical device field. In this role, you will be responsible for delivering

high-quality, compliant user documentation

that supports the safe and effective use of our products and meets strict regulatory requirements. You’ll work at the intersection of

engineering, regulatory, and product , transforming complex information into clear, structured, and user-focused content.

What You’ll Do Create, update, and manage

user manuals and technical documentation

in accordance with applicable regulations Ensure documentation is

clear, consistent, and aligned with usability and risk management requirements Collaborate closely with

R&D, Regulatory Affairs, and Product Management Gather and structure information from SMEs, engineering documents, and risk files Contribute to

structured authoring and CCMS-based documentation

(modular, topic-based, single-source) Manage the full documentation lifecycle:

versioning, change control, and traceability Coordinate

localization processes

with external translation partners Prepare and publish documentation for

digital distribution Support

audits and regulatory submissions

What We’re Looking For Bachelor’s or Master’s degree in

Humanities, Engineering, or a related STEM field At least 2 years of experience

in technical writing (ideally within a regulated environment) Fluent written and spoken

English

(additional languages are a plus) Excellent communication skills:

clear, structured, and precise writing is essential Strong ability to work cross-functionally and

proactively gather information Experience with a

CCMS

(Paligo is a plus) Solid xpavfwm understanding of

structured authoring methodologies

(topic-based writing, modular content, single-source publishing)

Mandatory Technical Skills Advanced proficiency in

Microsoft Office (Word & Excel)

— essential for authoring, formatting, and document management Working knowledge of

Adobe tools (InDesign, PDF suite)

for layout, publishing, and final document preparation

Nice to Have Experience in the

medical device industry Familiarity with regulatory frameworks ( MDR, ISO 13485, FDA ) Knowledge of Adobe Illustrator or similar tools for graphics