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Remote Medical Device Technical Writer Jobs in California

Technical Writer Client: Medical Device Manufacturing Company Duration: 6 Months (Possible ... Northridge, CA / Remote Shift: 1st Shift Responsibilities: * Create, edit, and maintain technical ...

Technical Writer

Beale Air Force Base, CA ยท 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

San Diego, CA ยท On-site +1

$55K - $126K/yr

Remote Work: No Job Number: R0242471 Location: San Diego,CA,US Share job via: Share Technical Writer The Opportunity: Join us and work with a Navy client to create, edit, publish, and maintain ...

Remote/Onsite (Based on Business Need) Employment Type: Full-Time Experience Level: Intermediate ... High attention to detail * Healthcare or medical device experience preferred * Excellent ...

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Remote Medical Device Technical Writer information

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.

What are popular job titles related to Remote Medical Device Technical Writer jobs in California? For Remote Medical Device Technical Writer jobs in California, the most frequently searched job titles are:
What job categories do people searching Remote Medical Device Technical Writer jobs in California look for? The top searched job categories for Remote Medical Device Technical Writer jobs in California are:
What cities in California are hiring for Remote Medical Device Technical Writer jobs? Cities in California with the most Remote Medical Device Technical Writer job openings:
Infographic showing various Remote Medical Device Technical Writer job openings in California as of August 2026, with employment types broken down into 85% Full Time, 10% Part Time, and 5% Contract. Highlights an 100% Remote job distribution.

Technical Writer

Three Point Solutions

Los Angeles, CA โ€ข Remote

Contractor

This job post hasย expired today.ย Applications are no longer accepted.


Job description

Job Title: Technical Writer

Client: Medical Device Manufacturing Company
Duration: 6 Months (Possible Extension)
Location: Northridge, CA / Remote
Shift: 1st Shift

Responsibilities:

  • Create, edit, and maintain technical documents, manuals, work instructions, and procedures.
  • Review and update documentation to reflect product and process changes.
  • Collaborate with Engineering, Quality, Regulatory, and Manufacturing teams.
  • Organize technical information into clear, user-friendly documentation.
  • Ensure documents comply with company standards and regulatory requirements.
  • Support document control, version management, and revision activities.
  • Proofread documents for grammar, formatting, consistency, and technical accuracy.
  • Prepare patient-facing and medical device documentation when required.
  • Maintain accurate documentation and support continuous process improvements.

Required Qualifications:

  • Bachelor's degree required.
  • Experience writing technical or patient-facing documentation.
  • Strong written and verbal communication skills.
  • Excellent attention to detail and organizational skills.
  • Proficiency in Microsoft Word, Excel, Outlook, and PowerPoint.

Preferred Qualifications:

  • Experience in the medical device or regulated industry.
  • Knowledge of document control and quality management systems.
  • Ability to work independently and collaborate with cross-functional teams.
  • Strong editing, proofreading, and technical writing skills.

#ZR

Company Description

As a leading contract, contract-to-hire and professional placement firm, Three Point Solution understands the importance of aligning our client with the right resource at the right time. We are committed to the highest caliber of service that will benefit our clients, candidates and employees. Unlike large, corporate style recruiting firms, we commit to individualized attention that uniquely positions us to bridge the communication gap between recruiter, employer and candidate. Our goal is to cultivate and maintain true partnerships with our clients and candidates.