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

As of May 30, 2026, the average hourly pay for part time 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 as a Part Time Medical Device Technical Writer, and why are they important?

A Part Time Medical Device Technical Writer requires strong technical writing abilities, knowledge of medical terminology, and familiarity with regulatory standards, typically supported by a degree in science, engineering, or communications. Proficiency with documentation tools like Microsoft Office, Adobe FrameMaker, and experience with quality management systems (QMS) and FDA or ISO regulations are common requirements. Excellent attention to detail, ability to communicate complex information clearly, and good time management are essential soft skills. These competencies ensure accurate, compliant, and user-friendly documentation, which is critical for regulatory approval and safe device operation.

How does a part-time medical device technical writer typically collaborate with engineering and regulatory teams?

As a part-time medical device technical writer, you'll frequently interact with engineering and regulatory teams to gather accurate technical information and ensure documentation complies with industry standards. Collaboration often involves attending meetings, reviewing product specifications, and incorporating feedback from subject matter experts. You'll need strong communication and organizational skills to manage document revisions and coordinate input from multiple stakeholders while working a flexible schedule. This cross-functional teamwork is essential to delivering clear, compliant, and user-friendly documentation.

What does a part time medical device technical writer do?

A part time medical device technical writer creates clear and accurate documentation related to medical devices, such as user manuals, regulatory submissions, instructions for use, and technical reports. They work closely with engineers, scientists, and regulatory teams to ensure that all materials meet industry standards and regulatory requirements. Working part time, they may focus on specific projects or support ongoing documentation needs while maintaining flexibility in their schedule.
What cities are hiring for Part Time Medical Device Technical Writer jobs? Cities with the most Part Time 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 Part Time Medical Device Technical Writer jobs? States with the most job openings for Part Time Medical Device Technical Writer jobs include:
Part Time Medical Device Technical Writer jobs near you
Technical Writer / Scientific Communications Specialist

Technical Writer / Scientific Communications Specialist

BeVera Solutions LLC

Riverdale, GA • On-site

Part-time

Posted 22 days ago

Job description

Description:

About BeVera Solutions, LLC

BeVera Solutions, LLC is a rapidly growing public health and professional services company that provides innovative solutions to federal and state agencies. Our team supports mission-critical programs through expertise in program management, communications, acquisition, data analytics, and public health initiatives. BeVera’s CEO champions a people-first culture where every employee is valued. The company supports this commitment by offering competitive compensation and meaningful, impactful work assignments.


Recognized as one of Atlanta’s Best Places to Work (2024 & 2025) by the Atlanta Business Chronicle, BeVera fosters a culture of integrity, excellence, and collaboration.


Job Description

BeVera Solutions, LLC is seeking a part-time Technical Writer / Scientific Communications Specialist to support a federal public health communications contract with the Centers for Disease Control and Prevention (CDC). This role supports the development of written communication products that translate technical and scientific information into clear and accessible materials for diverse audiences. The Technical Writer develops manuscripts, technical reports, conference abstracts, and campaign documentation that support public health communication initiatives and program reporting requirements.


NOTE: Position Contingent upon award of contract. This role is part of a pre-award candidate search for an upcoming federal government contract.


Requirements:
  • Develop manuscripts supporting public health communication initiatives.
  • Prepare technical and scientific reports for program documentation and reporting.
  • Draft conference abstracts, summaries, and supporting materials for dissemination of findings.
  • Develop campaign documentation including background materials, summaries, and supporting communication products.
  • Collaborate with research, communications, and program teams to translate technical information into clear written products.
  • Ensure written materials align with campaign messaging and federal communication standards.
  • Edit and review technical documents to ensure clarity, accuracy, and consistency.
  • Coordinate with project leadership to ensure documentation deliverables meet project schedules and requirements.
  • Ability to support project activities and coordination with federal stakeholders; travel may occasionally be requested.

Educational and Experience Qualifications

The following qualifications are the minimum requirements for successful performance under the anticipated contract.

  • Bachelor’s or Master’s degree in Communications, Journalism, Public Health, or a related field.
  • 5–8 years of experience preparing technical and scientific reports.
  • Demonstrated experience writing manuscripts, reports, and technical documentation.
  • Strong ability to translate complex scientific information into clear written materials.
  • Experience supporting public health or scientific communication initiatives.

Additional information

All information will be kept confidential according to EEO guidelines.


Equal Employment Opportunity Statement

BeVera Solutions is an Equal Opportunity Employer. Employment decisions are made solely on the basis of merit, qualifications, and business needs. We prohibit discrimination against any applicant or employee based on race, color, religion, sex, national origin, age, United States military veteran status, ancestry, marital status, family structure, medical condition (including genetic information), disability, or any other status protected under applicable federal, state, or local law, provided the essential functions of the job can be performed with or without reasonable accommodation.


BeVera complies with all applicable federal, state, and local equal employment opportunity laws and maintains a strictly merit-based hiring process consistent with current federal contracting requirements.

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