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Work From Home Medical Device Technical Writer Jobs in Raleigh, NC

Actalent

Technical Writer

Raleigh, NC · On-site +1

$50 - $68.50/hr

Ability to work effectively with cross-functional technical teams and translate complex concepts ... Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre ...

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Work From Home Medical Device Technical Writer information

See Raleigh, NC salary details

$13

$37

$64

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

As of Sep 7, 2026, the average hourly pay for work from home medical device technical writer in Raleigh, NC is $37.86, according to ZipRecruiter salary data. Most workers in this role earn between $28.03 and $45.82 per hour, depending on experience, location, and employer.

What does a work from home medical device technical writer do?

A Work From Home Medical Device Technical Writer is responsible for creating clear, accurate, and compliant documentation related to medical devices. This can include user manuals, regulatory submission documents, standard operating procedures, and technical reports. They collaborate with engineers, scientists, and regulatory teams to gather information and ensure that all documents meet industry standards and regulatory requirements. Working remotely, they use digital tools to communicate, manage projects, and deliver high-quality documentation to support the safe use and approval of medical devices.

What are the key skills and qualifications needed to thrive as a work from home medical device technical writer?

To thrive as a Work From Home Medical Device Technical Writer, you need strong technical writing skills, attention to detail, and a background in life sciences or engineering, often supported by a relevant degree. Familiarity with document management systems, regulatory guidelines (such as FDA or ISO standards), and authoring tools like Adobe FrameMaker or MS Word is typically required. Exceptional communication, self-motivation, and time management are essential soft skills for collaborating remotely and managing projects independently. These competencies ensure accurate, compliant, and user-friendly documentation that meets industry standards and facilitates safe device use.

How does a work from home medical device technical writer collaborate effectively with engineering and regulatory teams?

As a remote Medical Device Technical Writer, collaboration with engineering and regulatory teams is typically achieved through regular virtual meetings, shared documentation platforms, and project management tools. Writers are expected to proactively communicate and clarify technical information, review feedback, and ensure all documentation aligns with compliance standards. Building strong relationships with subject matter experts and maintaining clear channels for questions are key to efficiently producing accurate, regulatory-ready documents from a remote setting.

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For Work From Home Medical Device Technical Writer jobs in Raleigh, NC, the most frequently searched job titles are:

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Work From Home Medical Device Technical Writer jobs near you
Infographic showing various Work From Home Medical Device Technical Writer job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 20% Part Time, and 4% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $78,739 per year, or $37.9 per hour.

(Contract) Quality Technical Writer

Kymanox

Morrisville, NC • Remote

Contractor

Re-posted 16 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

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