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Medical Device Technical Writer Jobs (NOW HIRING)

Superbeo

Technical Writer

New York, NY · On-site

Technical Writer Job location: New York City, New York Job Duration: 3 Months, Contract to Hire ... Writing experience in the medical device industry or any relevant industry * Experience in writing ...

Pacer Group

Technical Writer

New York, NY · On-site

Technical Writer Job Location: New York City, NY Job Duration: 3 Months, Contract to Hire Job ... Writing experience in the medical device industry or any relevant industry * Experience in writing ...

millenniumsoft

Technical Writer

Salt Lake City, UT · On-site

Technical Writer Location: Salt Lake City, UT Duration: 6+ Months Contract Total Hours/week: 40.00 ... Experience in the medical device industry. Experience in continuous improvement projects ...

Medtronic

Technical Writer

Moundsview, MN · On-site

In this exciting role as a Technical Writer , you will produce customer-facing product ... Plan, research, develop, and write medical device labeling, and manage labeling deliverables as ...

Intuitive Surgical

Technical Writer

Sunnyvale, CA

Plan, write, and edit instructions for use (IFU) for medical device systems and instruments ... Work with interaction designers and technical illustrators to develop documentation images ...

Intuitive

Technical Writer

Sunnyvale, CA

Plan, write, and edit instructions for use (IFU) for medical device systems and instruments ... Work with interaction designers and technical illustrators to develop documentation images ...

Intuitive

Technical Writer

Sunnyvale, CA · On-site

Plan, write, and edit instructions for use (IFU) for medical device systems and instruments ... Work with interaction designers and technical illustrators to develop documentation images ...

The Contingent Plan

Technical Writer II

San Diego, CA · On-site

Pharmaceutical and/or medical device experience preferred. * Understanding of cGMP, ISO13485, and regulatory requirements * Three years of experience working as a technical writer. * Project ...

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Medical Device Technical Writer information

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How much do medical device technical writer jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for medical device technical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Medical Device Technical Writer position, and why are they important?

To thrive as a Medical Device Technical Writer, you need a deep understanding of medical terminology, regulatory standards, and technical writing best practices, typically supported by a degree in science, engineering, or technical communication. Familiarity with document management systems, authoring tools (such as Adobe FrameMaker or MadCap Flare), and knowledge of FDA or ISO documentation requirements are often essential. Exceptional attention to detail, strong organizational skills, and clear communication help writers collaborate effectively with engineers, clinicians, and regulatory teams. These skills and attributes ensure that complex medical device information is accurately documented, compliant with regulations, and accessible to diverse stakeholders.

What are the typical day-to-day responsibilities of a Medical Device Technical Writer?

As a Medical Device Technical Writer, your daily responsibilities usually include creating and revising user manuals, product instructions, and regulatory documentation for medical devices. You'll often collaborate closely with subject matter experts such as engineers, product managers, and quality assurance teams to gather technical details and ensure accuracy. You may also be involved in reviewing documents for compliance with industry regulations and standards, as well as participating in document audits or updates. The role requires balancing multiple projects and deadlines while ensuring all materials are clear, concise, and suitable for their intended audience.

What is a Medical Device Technical Writer job?

A Medical Device Technical Writer creates clear, accurate documentation for medical devices, including user manuals, regulatory submissions, and technical reports. They translate complex technical information into understandable content for various audiences, such as healthcare professionals, regulatory agencies, and end-users. This role requires knowledge of medical device regulations, engineering concepts, and technical writing standards. Strong attention to detail and collaboration with engineers, regulatory specialists, and subject matter experts are essential.

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Medical Device Technical Writer jobs near you
Sr. Technical Writer

Sr. Technical Writer

Integrated Resources INC

Bridgewater, NJ

Other

Posted 6 days ago

Job description

Company Description

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

Job Description

Position: Sr. Technical Writer

Duration: 6+ contract

Location: Bridgewater, NJ

Direct Client: Immediate interview

SR tech writer. The person has to be very familiar with working in an R&D shop writing very detailed Functional Specifications working with developers and understanding the software development life cycle.

The candidate should be able to write very precise business and technical requirements in order to write Requirement Specification documents. I want a senior level persons who can self

Manage and motivate and some biology, life science, pharma, biotech or cro experience.

Sr Technical Writer/Lead to assist with writing requirements, FS, management of documents, coordination, knowledge of document management tools like Alfresco, SVN 9 version control, Robohelp, Adobe, Word, etc. Need excellent writing skills, technical background and experience of clinical trials domain/ CRO/Medical Device is must. . Experience in Pharma, CRO, Medical Device or Biotech industry is a must. Long Term Contract opportunity.

Additional Information

Regards,

Nagesh

732-429-1641

Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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