Technical Writer at GE HealthCare

Ideal for a mid-level technical writer with at least 2 years of experience, preferably in the medical device industry, who can translate complex technical infor

Work type: onsite

Location: Herlev

Type: Full-time

Summary

Ideal for a mid-level technical writer with at least 2 years of experience, preferably in the medical device industry, who can translate complex technical information into clear documentation. **What makes it worth a look...** This full-time, on-site role at GE HealthCare in Herlev, Denmark, offers the chance to work with a global leader in medical technology. The company highlights its comprehensive rewards package designed to support ambition and flexibility. **You might be a good fit if you...** * Have 2+ years of experience as a technical writer. * Are proficient with Microsoft Office (Word, PowerPoint, Excel). * Have experience with a Content Management System (CMS) like Astoria or Tridion. * Medical device experience is preferred.

Job Description

# Job Description Summary

GE Healthcare is looking for a talented technical writer to join our medical devices team in Herlev, Denmark.

Activities contributing to the design and development of products, solutions and systems. Includes activities linked to technical improvement of existing products and components Impacts quality of own work and the work of others on the team. Executes standard operational/technical tasks typically subject to instructions and work routines. There is latitude to rearrange the sequence to complete task/duties based on changing work situations.

GE HealthCare is a leading global medical technology and digital solutions innovator with over 100 years of healthcare industry experience and around 50,000 employees globally. We enable clinicians to make faster, more informed decisions through intelligent devices, data analytics, applications and services, supported by our Edison intelligence platform. We operate at the center of an ecosystem working toward precision health - digitizing healthcare, helping drive productivity and improving outcomes for patients, providers, health systems and researchers around the world.

# Job Description

## Responsibilities

• Partner with project managers, R&D, marketing, and regulatory affairs to gather input, clarify requirements, and produce clear, accurate documentation that supports internal and external stakeholders.

• Create, update, review, and release technical documentation (e.g., user manuals, instructions for use, and product data sheets) in line with established processes.

• Support translation and localization activities by preparing source content, coordinating reviews, and helping ensure translated deliverables meet quality expectations.

• Coordinate day-to-day documentation tasks with other team members in Technical Documentation and provide regular status updates on assigned work.

• Follow corporate documentation standards, templates, and style guidelines to ensure consistency across deliverables.

• Contribute to knowledge management by maintaining and improving documentation templates, reusable content, and internal guidelines.

• Identify opportunities to improve documentation quality and efficiency, and share practical best practices with the team.

• Apply relevant regulations, policies, and internal procedures when developing and maintaining documentation, in collaboration with regulatory and quality stakeholders.

## Qualifications

• 2+ years of experience as a technical writer or technical documentation specialist (medical device experience is preferred).

• Education in technical writing, technical communication, engineering, linguistics, or a related field is an advantage.

• Strong written and verbal communication skills in English, with attention to detail.

• Proficiency with Microsoft Office (Word, PowerPoint, and Excel).

• Experience working with a Content Management System (CMS) such as Astoria or Tridion (or similar tools).

• Familiarity with Adobe InDesign and Illustrator is a plus.

• Proactive and resourceful approach to finding and validating information with SMEs.

• Strong interpersonal and collaboration skills, including the ability to communicate effectively across functions and geographies.

• Experience working with global development or production sites is a plus.

• Ability to work independently on assigned documentation tasks while contributing effectively within a team environment.

• Structured, problem-solving mindset with the ability to handle multiple priorities in a fast-paced setting.

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.

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