Globus Medical

Medical Devices

TechnicalWriter

Massachusetts, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid candidates.

The Brief

“Technical Writer at Globus Medical. Skills: Technical writing, Medical devices, Regulatory compliance. Create clear, accurate, and compliant technical documentation. Translate complex imaging concepts into user-friendly documentation”

Industry & Context.

Medical Devices
Problems you'll solve

Analytical and problem-solving skills

Eligibility Requirements

Climb or stoop, Kneel, Crouch or crawl, Lift and/or move up to 10 pounds, Occasionally lift and/or move up to 25 pounds, Specific vision abilities required, Close vision, Distance vision, Color vision, Peripheral vision, Depth perception, Capacity to adjust focus

What They're Looking For.

Must Have

Proven working experience in technical writing of software documentation, Exceptional attention to detail and accuracy, Analytical and problem-solving skills, Ability to learn complex technical systems quickly, Comfort working in highly regulated environment, Ability to quickly grasp complex technical concepts and make them easily understandable in text and pictures, Working knowledge of Microsoft Office, Minimum of 5 years of experience in technical writing, Experience writing documentation for regulated products (FDA, CE, ISO), Excellent written and verbal communication skills, Ability to manage multiple projects and deadlines simultaneously

Nice to Have

Bachelor’s degree in computer science, Engineering or equivalent, preferably in medical devices, healthcare, or regulated industries, understanding of medical imaging workflows, terminology, or clinical environments

What You'll Do.

and compliant technical documentation

Translate complex imaging concepts into user-friendly documentation

Ensure compliance with company policies

Maintain compliance with US FDA regulations

Maintain compliance with international medical device regulations

Maintain compliance with ISO 13485 quality system requirements

Work with internal teams

Obtain in-depth understanding of product

Produce high-quality documentation

Create SOPs and procedures

Test and verify FS procedures

Create and maintain System Functionality

Create and maintain Installation procedures

Create and maintain Preventative Maintenance

Create and maintain Accuracy Checklist

Analyze existing and potential content

Focus on reuse opportunities

Focus on single-sourcing opportunities

Create and maintain information architecture

Research technical writing tools

Standardize templates for ease creation

Standardize templates for ease maintenance

Ensure documentation complies with applicable standards

Represent FS in the DCO process

Maintain document version control

Maintain change histories

Maintain review workflows

Maintain FS Calibrated equipment inventory

Maintain FS tool inventory

Adhere to company Code of Conduct

Adhere to AdvaMed Code

Adhere to MedTech Code

Adhere to all company policies

Ensure compliance with governmental laws

Complete introductory training

Complete annual training

Maintain knowledge of compliance

Represent the company professionally

Uphold highest standards of ethical business practices

Uphold highest standards of socially responsible conduct

How You'll Work.

Team & Collaboration

Partnering with researchers and educators; Work with internal teams; Translate complex imaging concepts; Bridges engineering, clinical, regulatory, and quality teams; Work with system Field Service Team; Work with Product Trainer; Work with Engineering staff; Collaborative mindset; Teamwork

Communication Scope

Excellent written communication skills; Excellent verbal communication skills

Process & Methodology

Independently manage time/schedule, Manage multiple projects, Manage deadlines simultaneously

Full Job Description

At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons and healthcare providers who treat them. We embrace a culture of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and outcomes of surgery so patients can resume their lives as quickly as possible. ** _Position Summary_****:** Our rapidly growing medical imaging, navigations and robotics division is searching for a field service technical writer. The candidate will create clear, accurate, and compliant technical documentation for medical imaging products and systems. This role bridges engineering, clinical, regulatory, and quality teams to translate complex imaging concepts into user-friendly documentation that supports product development, regulatory submissions, and end-user adoption. While ensuring compliance with all company policies & procedures and maintaining compliance with US FDA and international medical device regulations and ISO 13485 quality system requirements. The job requires the individual to be a self-starter and team player with the ability to work well without close supervision, can independently manage time/schedule and function well in a challenging and fast paced environment. Must be enthusiastic, positive, even tempered and have strong skills in areas of dependability, interpersonal relationships, flexibility and maturity. **_Essential Functions_****:** * Work with internal teams to obtain an in-depth understanding of the product and the documentation requirements * Produce high-quality documentation that meets applicable standards with system Field Service Team, Product Trainer and Engineering staff to create SOPs and procedures across all products. * Test and Verify all FS procedures from Engineering * Create and Mai

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