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Remote Medical Device Technical Writer Jobs (NOW HIRING)

Job Role - Technical Writer Location - Secaucus, NJ(Remote) Qualifications: Education Preferred ... Knowledge of medical terminology Knowledge of Adobe Framemaker Knowledge of GitLab and GitHub ...

Primarily remote work with some planned onsite work in Jackson, MS Remote with occasional travel onsite Rate: xxx/hr on C2C All Inclusive or xxx/hr on W2 Without Benefits State Agency: MS MDCPS ...

$127K - $190K/yr

As a Technical Writer, you will join a global, remote-first environment where you will shape how developers and technical users interact with complex software solutions. You will own documentation ...

Most of our positions are remote, offering flexibility while working on impactful projects. Key Skills amp; Qualifications We're Looking For: * Technical Writing: Proven experience in creating clear ...

Stay informed about changes to relevant medical device regulations and standards and ensure that ... technical writing in the medical device sector. Other Helpful Knowledge, Skills and Abilities ...

Job Title: Technical Writer Location: Denver, CO - Remote Duration: 1 Months Contract QUALIFICATIONS: Microsoft Excel 2010/2013 Duties and Responsibilities: This person would be transcribing past ...

Remote Position Overview The State Court Administrator's Office (Court Services Division) is seeking a Technical Writer/Data Specialist for a short-term, one-month project . Important: This ...

Technical Writer

$50K - $75K/yr

... is seeking a Technical Writer to support our federal software development program. The ideal ... This is a remote, full-time, W2 role. Key Responsibilities: * Develop, edit, and maintain end-user ...

Technical Writer

Chantilly, VA · On-site +1

$120K - $160K/yr

Technical Writer/Ed Schedule: Full-Time Shift: Day Job Travel: Yes - 25% of the time Minimum ... None Potential for Remote Work: ORA_HYBRID Description SAIC is a trusted leader in delivering ...

Technical Writer

Beale Air Force Base, CA · On-site +1

$120K - $160K/yr

Technical Writer/Ed Schedule: Full-Time Shift: Day Job Travel: Yes - 25% of the time Minimum ... None Potential for Remote Work: ORA_HYBRID Description SAIC is a trusted leader in delivering ...

While currently defined as a remote position, this will become an on-site role when space on the ... Experience working in a regulated environment, preferably in medical device * Comfortable working ...

Remote Summary Overview : The Office of Integrated Food Safety System Partnerships (OIFSSP) leads ... The technical writer will develop, revise, and maintain documentation for operational and ...

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Remote Medical Device Technical Writer information

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$14

$38

$57

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

As of Aug 1, 2026, the average hourly pay for remote 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 is the difference between Remote Medical Device Technical Writer vs Remote Regulatory Affairs Specialist?

AspectRemote Medical Device Technical WriterRemote Regulatory Affairs Specialist
CredentialsTypically requires a degree in life sciences, engineering, or related field; certifications like RMT or technical writing certifications are commonRequires degrees in life sciences, law, or regulatory fields; certifications like RAC are often preferred
Work EnvironmentPrimarily writes and edits technical documents remotely for medical device companiesFocuses on regulatory submissions, compliance, and communication with authorities, often remotely
Industry UsageUsed across medical device companies, biotech, and healthcare tech firmsCommon in medical device, pharmaceutical, and biotech industries

While both roles require knowledge of medical devices and regulatory standards, the Remote Medical Device Technical Writer primarily creates technical documentation, whereas the Remote Regulatory Affairs Specialist manages regulatory compliance and submissions. Both roles often work remotely and require relevant industry experience, but their core responsibilities differ significantly.

More about Remote Medical Device Technical Writer jobs
What cities are hiring for Remote Medical Device Technical Writer jobs? Cities with the most Remote Medical Device Technical Writer job openings:
What are the most commonly searched types of Medical Device Technical Writer jobs? The most popular types of Medical Device Technical Writer jobs are:
What states have the most Remote Medical Device Technical Writer jobs? States with the most job openings for Remote Medical Device Technical Writer jobs include:
Infographic showing various Remote Medical Device Technical Writer job openings in the United States as of July 2026, with employment types broken down into 62% Full Time, 13% Part Time, and 25% Contract. Highlights an 100% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

(Contract) Quality Technical Writer

Kymanox

Morrisville, NC • Remote

Contractor

Posted 10 days ago


Job description

Job Description:

Is Kymanox the right fit for you?

You want to make a difference and have an impact...

You enjoy having an influence in your day-to-day work...

You are motivated by working alongside a team filled with

subject matter experts who will help you learn and grow...

You wake up every day and do what you do

... because patients deserve better.

If this sounds like you, you've come to the right place.

The Technical Writer - General QMS (Contract)will perform technical writing and client support on a site readiness project authoring a range of engineering, compliance, and commercialization Standard Operating Procedures (SOPs).

Responsibilities:

  • Technical writing may include any of the following focus areas:
    1. Manufacturing equipment and processes
    2. Quality Control Laboratory instruments and methods
    3. Utility systems
    4. Facilities and maintenance equipment
    5. Logistics and warehousing processes
    6. Quality Assurance processes
    7. Environment, Health, and Safety processes
    8. Warehouse and Supply Chain
    9. Information Technology
    10. Training content.

Educational Background:

  • The ideal candidate will have a bachelor's degree in any Engineering discipline (prefer Biomedical, Mechanical, or Chemical engineering) or other STEM discipline (Biology, Chemistry, other) from an accredited institution or equivalent.

Experience:

  • A minimum of 3 to 5 years of experience in development and/or manufacturing in the pharmaceutical, biotechnology, combination product, and/or medical device sectors is required.
  • Senior level 8-15 years of experience in technical writing within the Pharma, Medical Device, or BioTech industries is desired.

Desired Aptitude and Skill Set:

  • Resourceful
  • Extremely detail oriented
  • Ability to work effectively with remote team members
  • Highly organized
  • Self-directing, self-pacing
  • Excellent written and oral English communication skills
  • Understanding of own limitations
  • Ability to solicit and utilize subject matter expert input
  • Fast learner
  • Pleasant and positive communication style
  • Strong customer-service aptitude
  • Ability to motivate self, team members, and direct reports
  • High energy level
  • Excellent problem-solving skills
  • Seasoned soft skills (i.e., high EQ)
  • Team player

Compensation:

Hourly rate is commensurate with experience, qualifications, and other intangibles evident during the interview process - as well as market conditions.

Travel:

Travel may be necessary to support client work.

About Kymanox:
Join Kymanox - a life sciences professional services company dedicated to life sciences who has successfully delivered over 4000 projects across 20+ countries. Become a member of a dynamic, fulfilling team that helps a broad range of life science products get to market more quickly, more affordably, and with the highest quality and safety standards possible in today's biotechnology, pharmaceutical, medical device, and combination product industries. With a reputation of providing unparalleled professional services and our highly collaborative team of engineering, compliance, and project management experts, Kymanox provides an outstanding opportunity for learning and career advancement. Kymanox encourages team members, especially new graduates, and young professionals, to work on a variety of projects to gain increased learnings in Kymanox's service offerings and the life science industry as a whole.

Kymanox is looking for motivated individuals who want to solve problems in the life science industries while doing the work they love and helping get modern medicines that enhance and save patient lives to market. Kymanox provides professional services related to engineering, compliance, and project management. We service clients ranging from Fortune 100 companies to virtual start-up companies. The company was founded in 2004 and has been growing steadily since its inception. Our corporate HQ is based in Research Triangle Park, NC.

To learn more about our company, please visit our website:Life Science Solutions | Kymanox

Kymanox is an equal-opportunity employer and works diligently to protect the rights of job seekers by following all local, state, and federal laws as well as best Human Resource (HR) practices in the Life Science industry.

Employment Type: Contractor