ZipRecruiter

Log In

2

Entry Level Medical Device Technical Writer Jobs

Three Point Solutions

Technical Writer

Northridge, CA · On-site

$20 - $22/hr

Medical Device Manufacturing Company Duration: 6 Months (Possible Extension) Location: Northridge, CA / Remote Shift: 1st Shift Responsibilities: * Create, edit, and maintain technical documents ...

Jobtailor

NY · On-site

$75 - $110/hr

Experience developing controlled or regulated documentation, preferably in a medical device ... Previous experience as a Technical Writer, Medical Writer, or Regulatory Communications specialist

Marquee Staffing - OC

Be Seen First

$20/hr. Medical Device Assembler Clean Room First Shift

Irvine, CA · On-site

$19 - $20/hr

... entry level medical device assembly. You are welcome to apply too Location Irvine. Pay Rate ... Use a computer or write when needed. * Wear PPE as required. Physical Requirements * Stand, walk ...

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 ...

MiniMed

Technical Writer

Los Angeles, CA · On-site

$64K - $110K/yr

About the Role The Technical Writer scopes, revises and drafts a variety of patient-facing ... Develop of a working understanding of medical device products * Work with required subject matter ...

next page

Showing results 1-20

All JobsEducation JobsBusiness Education JobsTechnical Writer JobsEntry Level Medical Device Technical Writer Jobs

Entry Level Medical Device Technical Writer information

See salary details

$14

$38

$57

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

As of Aug 23, 2026, the average hourly pay for entry level 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 Entry Level Medical Device Technical Writer vs Medical Device Quality Assurance Associate?

AspectEntry Level Medical Device Technical WriterMedical Device Quality Assurance Associate
Required CredentialsBachelor's in Life Sciences, Writing or related field; certifications like RAPS or regulatory writing helpfulBachelor's in Engineering, Life Sciences, or related; certifications like ISO or GMP training beneficial
Work EnvironmentOffice setting, documentation teams, regulatory departmentsManufacturing facilities, quality labs, compliance departments
Employer & Industry UsageMedical device companies, regulatory agencies, consulting firmsManufacturers, medical device firms, healthcare companies
Common Search & ComparisonYesYes

While both roles support the medical device industry, Entry Level Medical Device Technical Writers focus on creating and managing technical documentation, whereas Medical Device Quality Assurance Associates ensure product compliance and quality standards. Both positions require relevant certifications and work within similar industry environments, but their core responsibilities differ significantly.

How can I get into entry level medical device technical writing with no experience?

Entry level medical device technical writers typically need strong writing skills, basic knowledge of medical devices, and familiarity with regulatory standards like FDA or ISO. Gaining experience through internships, online courses, or certifications such as the Certified Professional Technical Communicator (CPTC) can improve prospects. Building a portfolio of writing samples and understanding medical terminology helps to enter the field without prior direct experience.
More about Entry Level Medical Device Technical Writer jobs

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 Entry Level Medical Device Technical Writer jobs?

States with the most job openings for Entry Level Medical Device Technical Writer jobs include:

What job categories do people searching Entry Level Medical Device Technical Writer jobs look for?

The top searched job categories for Entry Level Medical Device Technical Writer jobs are:

Entry Level Medical Device Technical Writer jobs near you
Infographic showing various Entry Level Medical Device Technical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

Medical Device Technical Writer: 25-03652 at Akraya, Inc. Sunnyvale, CA

Downtown Boulder Partnership

Sunnyvale, CA • On-site

$171.92/hr

Other

Posted 5 days ago

Job description

Medical Device Technical Writer (Job ID: 25-03652)

Location: Sunnyvale, CA (Hybrid) • Contract Type: W2 • Duration: 12+ Months • Pay Range: $60–$65 per hour

Job Summary: We are seeking two highly skilled QMS Technical Writers requiring 3‑5 years of experience in a regulated environment, to develop and maintain clear, compliant, and user‑friendly internal process documentation. The successful candidates will collaborate closely with cross‑functional teams and SMEs, ensuring all documentation adheres to company and regulatory guidelines. This self‑directed role demands excellent time management and communication skills, thriving in a fast‑paced setting.

Key Responsibilities
  • Write, edit, and maintain internal process documentation in line with company and regulatory standards.
  • Provide writing support for teams transitioning to new templates and guidelines, developing process documentation flowcharts.
  • Ensure compliance with Quality, Document Control, and Good Documentation Practice (GDP) guidelines.
  • Act as lead writer on projects, mentoring other writers, keeping abreast of compliance requirements, sharing expertise, and participating in regulatory training.
  • Manage multiple project deliverables under tight deadlines, prioritizing effectively and collaborating with project teams.
Must‑Have Skills
  • Exceptional writing, editing, and grammar skills in a regulated environment.
  • Strong organizational and time‑management capabilities.
  • Proficiency in Microsoft Word and Visio, with a solid understanding of Adobe Illustrator or Photoshop.
Domain Experience

Previous experience in the medical devices sector or other regulated environments is required, highlighting a deep understanding of the document control process and familiarity with decision tracking software like OneNote, Excel, and Smartsheet.

Primary Skills
  • SOPs (Expert)
  • Regulations/Medical Devices (Advanced)
  • Document Control (Expert)
  • Excel/Smartsheet/OneNote (Intermediate)
  • Meeting Leadership (Advanced)
#J-18808-Ljbffr

Apply